Name

Craniofacial anomalies and anterior segment dysgenesis syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

craniofacial anomalies and anterior segment dysgenesis syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniofacial anomalies and anterior segment dysgenesis syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Foveal hypoplasia and anterior segment dysgenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Foveal hypoplasia and anterior segment dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Foveal Hypoplasia and Anterior Segment Dysgenesis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Foveal Hypoplasia and Anterior Segment Dysgenesis from the curated CTD Gene-Disease Associations dataset.

foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis Gene Set

From OMIM Gene-Disease Associations

genes associated with the foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

Anterior segment mesenchymal dysgenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Anterior segment mesenchymal dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anterior segment mesenchymal dysgenesis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anterior segment mesenchymal dysgenesis from the curated CTD Gene-Disease Associations dataset.

anterior segment dysgenesis Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior segment dysgenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior segment mesenchymal dysgenesis Gene Set

From OMIM Gene-Disease Associations

genes associated with the anterior segment mesenchymal dysgenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniofacial dysmorphism, skeletal anomalies, and mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

anterior segment anomalies with or without cataract Gene Set

From OMIM Gene-Disease Associations

genes associated with the anterior segment anomalies with or without cataract phenotype from the curated OMIM Gene-Disease Associations dataset.

Defective CYP26B1 causes Radiohumeral fusions with other skeletal and craniofacial anomalies (RHFCA) Gene Set

From Reactome Pathways

proteins participating in the Defective CYP26B1 causes Radiohumeral fusions with other skeletal and craniofacial anomalies (RHFCA) pathway from the Reactome Pathways dataset.

abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; congenital heart defects; craniofacial abnormalities; ectodermal dysplasia; heart defects, congenital; noonan syndrome; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anterior pituitary dysgenesis Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior pituitary dysgenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the anterior segment of the eye Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the anterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the anterior segment of the eye Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the anterior segment of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

aplasia/hypoplasia affecting the anterior segment of the eye Gene Set

From HPO Gene-Disease Associations

genes associated with the aplasia/hypoplasia affecting the anterior segment of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior segment of eye aplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior segment of eye aplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal anterior eye segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal anterior eye segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome from the curated CTD Gene-Disease Associations dataset.

cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ANTLEY-BIXLER SYNDROME WITH GENITAL ANOMALIES AND DISORDERED STEROIDOGENESIS from the curated CTD Gene-Disease Associations dataset.

Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome from the curated CTD Gene-Disease Associations dataset.

antley-bixler syndrome with genital anomalies and disordered steroidogenesis Gene Set

From OMIM Gene-Disease Associations

genes associated with the antley-bixler syndrome with genital anomalies and disordered steroidogenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Psychomotor retardation, epilepsy, and craniofacial dysmorphism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Psychomotor retardation, epilepsy, and craniofacial dysmorphism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

psychomotor retardation, epilepsy, and craniofacial dysmorphism Gene Set

From OMIM Gene-Disease Associations

genes associated with the psychomotor retardation, epilepsy, and craniofacial dysmorphism phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects phenotype from the curated OMIM Gene-Disease Associations dataset.

Craniofacial deafness hand syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Craniofacial deafness hand syndrome from the curated CTD Gene-Disease Associations dataset.

abnormalities, multiple; craniofacial abnormalities; mental retardation; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; craniofacial abnormalities; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

craniofacial abnormalities; growth disorders; learning disorders; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease craniofacial abnormalities; growth disorders; learning disorders; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; congenital abnormalities; craniofacial abnormalities; syndrome; translocation, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; congenital abnormalities; craniofacial abnormalities; syndrome; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; craniofacial abnormalities; mouth abnormalities; pallister-hall syndrome; polydactyly; syndactyly Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; craniofacial abnormalities; mouth abnormalities; pallister-hall syndrome; polydactyly; syndactyly in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

craniofacial-deafness-hand syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniofacial-deafness-hand syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Anterior hypothalamic nucleus, anterior part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior hypothalamic nucleus, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

abnormal anterior commissure pars anterior morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal anterior commissure pars anterior morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease 46,XX SEX REVERSAL WITH DYSGENESIS OF KIDNEYS, ADRENALS, AND LUNGS from the curated CTD Gene-Disease Associations dataset.

Sudden Infant Death with Dysgenesis of the Testes Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sudden Infant Death with Dysgenesis of the Testes Syndrome from the curated CTD Gene-Disease Associations dataset.

sudden infant death with dysgenesis of the testes syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the sudden infant death with dysgenesis of the testes syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

athabaskan brainstem dysgenesis syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the athabaskan brainstem dysgenesis syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly with mental retardation and digital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly with mental retardation and digital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies, type A14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniosynostosis and dental anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Craniosynostosis and dental anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aplasia cutis congenita, reticulolinear, with microcephaly, facial dysmorphism, and other congenital anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Craniosynostosis, anal anomalies, and porokeratosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Craniosynostosis, anal anomalies, and porokeratosis from the curated CTD Gene-Disease Associations dataset.

Bifid Nose With Or Without Anorectal And Renal Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bifid Nose With Or Without Anorectal And Renal Anomalies from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 2 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 6 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 5 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 4 from the curated CTD Gene-Disease Associations dataset.

Microcephaly with Mental Retardation and Digital Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microcephaly with Mental Retardation and Digital Anomalies from the curated CTD Gene-Disease Associations dataset.

pituitary anomalies and holoprosencephaly-like features. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pituitary anomalies and holoprosencephaly-like features. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

robin sequence with cleft mandible and limb anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the robin sequence with cleft mandible and limb anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

{congenital anomalies of kidney and urinary tract, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {congenital anomalies of kidney and urinary tract, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

craniosynostosis and dental anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniosynostosis and dental anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type a, 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal opacification and other ocular anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal opacification and other ocular anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

aplasia cutis congenita, reticulolinear, with mmicrocephaly, facial dysmorphism and other congenital anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the aplasia cutis congenita, reticulolinear, with mmicrocephaly, facial dysmorphism and other congenital anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

bifid nose with or without anorectal and renal anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the bifid nose with or without anorectal and renal anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Saethre-Chotzen syndrome with eyelid anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Saethre-Chotzen syndrome with eyelid anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Immunodeficiency-centromeric instability-facial anomalies syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency-centromeric instability-facial anomalies syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple congenital anomalies-hypotonia-seizures syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease IMMUNODEFICIENCY-CENTROMERIC INSTABILITY-FACIAL ANOMALIES SYNDROME 1 from the curated CTD Gene-Disease Associations dataset.

Saethre-Chotzen Syndrome with Eyelid Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Saethre-Chotzen Syndrome with Eyelid Anomalies from the curated CTD Gene-Disease Associations dataset.

ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ANTLEY-BIXLER SYNDROME WITHOUT GENITAL ANOMALIES OR DISORDERED STEROIDOGENESIS from the curated CTD Gene-Disease Associations dataset.

coronary vessel anomalies; mucocutaneous lymph node syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary vessel anomalies; mucocutaneous lymph node syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antley-bixler syndrome without genital anomalies or disordered steroidogenesis Gene Set

From OMIM Gene-Disease Associations

genes associated with the antley-bixler syndrome without genital anomalies or disordered steroidogenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency-centromeric instability-facial anomalies syndrome-2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency-centromeric instability-facial anomalies syndrome-2 phenotype from the curated OMIM Gene-Disease Associations dataset.

saethre-chotzen syndrome with eyelid anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the saethre-chotzen syndrome with eyelid anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

?multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?multiple congenital anomalies-hypotonia-seizures syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple congenital anomalies-hypotonia-seizures syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple congenital anomalies-hypotonia-seizures syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the multiple congenital anomalies-hypotonia-seizures syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency-centromeric instability-facial anomalies syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency-centromeric instability-facial anomalies syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

Craniofacial Abnormalities Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Craniofacial Abnormalities from the curated CTD Gene-Disease Associations dataset.

Craniofacial Dysostosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Craniofacial Dysostosis from the curated CTD Gene-Disease Associations dataset.

acrocephalosyndactylia; craniofacial dysostosis; craniosynostoses; plagiocephaly, nonsynostotic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acrocephalosyndactylia; craniofacial dysostosis; craniosynostoses; plagiocephaly, nonsynostotic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; craniofacial abnormalities Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; craniofacial abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

craniofacial Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term craniofacial in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

craniofacial suture morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the craniofacial suture morphogenesis biological process from the curated GO Biological Process Annotations dataset.

craniofacial disproportion Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the craniofacial disproportion phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

craniofacial osteosclerosis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the craniofacial osteosclerosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

craniofacial dysostosis Gene Set

From HPO Gene-Disease Associations

genes associated with the craniofacial dysostosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

craniofacial dystonia Gene Set

From HPO Gene-Disease Associations

genes associated with the craniofacial dystonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

craniofacial disproportion Gene Set

From HPO Gene-Disease Associations

genes associated with the craniofacial disproportion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

craniofacial hyperostosis Gene Set

From HPO Gene-Disease Associations

genes associated with the craniofacial hyperostosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

craniofacial osteosclerosis Gene Set

From HPO Gene-Disease Associations

genes associated with the craniofacial osteosclerosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Craniofacial Abnormalities Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Craniofacial Abnormalities phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Craniofacial Dysostosis Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Craniofacial Dysostosis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

SWR1-complex protein 5/Craniofacial development protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the SWR1-complex protein 5/Craniofacial development protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

absent craniofacial bones Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent craniofacial bones phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

craniofacial phenotype Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the craniofacial phenotype phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal craniofacial development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal craniofacial development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

craniofacial asymmetry Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the craniofacial asymmetry phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal craniofacial morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal craniofacial morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal craniofacial bone morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal craniofacial bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

craniofacial-skeletal-dermatologic dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniofacial-skeletal-dermatologic dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

craniofacial region Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue craniofacial region from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

craniofacial region Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue craniofacial region in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease digeorge syndrome; pharyngeal pouch; syndrome; velo-cardio-facial syndrome; 22q11 deletion syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Irido-corneo-trabecular dysgenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Irido-corneo-trabecular dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Reticular dysgenesis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Reticular dysgenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ovarian dysgenesis 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ovarian dysgenesis 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ovarian dysgenesis 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ovarian dysgenesis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

46,XY gonadal dysgenesis, partial, with minifascicular neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 46,XY gonadal dysgenesis, partial, with minifascicular neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

46,XY gonadal dysgenesis, complete, dhh-related Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 46,XY gonadal dysgenesis, complete, dhh-related phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gonadal dysgenesis with auditory dysfunction, autosomal recessive inheritance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gonadal Dysgenesis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gonadal Dysgenesis from the curated CTD Gene-Disease Associations dataset.

Gonadal Dysgenesis, 46,XX Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gonadal Dysgenesis, 46,XX from the curated CTD Gene-Disease Associations dataset.

OVARIAN DYSGENESIS 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease OVARIAN DYSGENESIS 1 from the curated CTD Gene-Disease Associations dataset.

Athabaskan brainstem dysgenesis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Athabaskan brainstem dysgenesis from the curated CTD Gene-Disease Associations dataset.

46,XY Gonadal Dysgenesis, Complete or Partial, DHH-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease 46,XY Gonadal Dysgenesis, Complete or Partial, DHH-Related from the curated CTD Gene-Disease Associations dataset.

RENAL TUBULAR DYSGENESIS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease RENAL TUBULAR DYSGENESIS from the curated CTD Gene-Disease Associations dataset.

46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease 46,Xy Gonadal Dysgenesis, Partial, With Minifascicular Neuropathy from the curated CTD Gene-Disease Associations dataset.

Reticular dysgenesis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Reticular dysgenesis from the curated CTD Gene-Disease Associations dataset.

Ovarian Dysgenesis 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ovarian Dysgenesis 2 from the curated CTD Gene-Disease Associations dataset.

Gonadal Dysgenesis, 46,XY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gonadal Dysgenesis, 46,XY from the curated CTD Gene-Disease Associations dataset.

Gonadal dysgenesis XX type deafness Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Gonadal dysgenesis XX type deafness from the curated CTD Gene-Disease Associations dataset.

gonadal dysgenesis Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease gonadal dysgenesis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

reticular dysgenesis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease reticular dysgenesis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

46 xy gonadal dysgenesis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease 46 xy gonadal dysgenesis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

gonadal dysgenesis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease gonadal dysgenesis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

mixed gonadal dysgenesis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease mixed gonadal dysgenesis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

hypothyroidism; thyroid dysgenesis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypothyroidism; thyroid dysgenesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thyroid dysgenesis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease thyroid dysgenesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gonadal dysgenesis, 46,xy; infertility, male; sudden infant death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gonadal dysgenesis, 46,xy; infertility, male; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gonadal dysgenesis, 46,xy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gonadal dysgenesis, 46,xy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital abnormalities; hypothyroidism; thyroid dysgenesis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital abnormalities; hypothyroidism; thyroid dysgenesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital hypothyroidism; thyroid dysgenesis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital hypothyroidism; thyroid dysgenesis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dysgenesis Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term dysgenesis in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

gonadal dysgenesis Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease gonadal dysgenesis in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

testicular dysgenesis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the testicular dysgenesis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

thyroid dysgenesis Gene Set

From HPO Gene-Disease Associations

genes associated with the thyroid dysgenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

gonadal dysgenesis Gene Set

From HPO Gene-Disease Associations

genes associated with the gonadal dysgenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

testicular dysgenesis Gene Set

From HPO Gene-Disease Associations

genes associated with the testicular dysgenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

adrenal gland dysgenesis Gene Set

From HPO Gene-Disease Associations

genes associated with the adrenal gland dysgenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

gonadal dysgenesis, male Gene Set

From HPO Gene-Disease Associations

genes associated with the gonadal dysgenesis, male phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

unilateral primary pulmonary dysgenesis Gene Set

From HPO Gene-Disease Associations

genes associated with the unilateral primary pulmonary dysgenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

posterior pituitary dysgenesis Gene Set

From HPO Gene-Disease Associations

genes associated with the posterior pituitary dysgenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

renotubular dysgenesis Gene Set

From HPO Gene-Disease Associations

genes associated with the renotubular dysgenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

dysgenesis of the cerebellar vermis Gene Set

From HPO Gene-Disease Associations

genes associated with the dysgenesis of the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

intrahepatic biliary dysgenesis Gene Set

From HPO Gene-Disease Associations

genes associated with the intrahepatic biliary dysgenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

parathyroid dysgenesis Gene Set

From HPO Gene-Disease Associations

genes associated with the parathyroid dysgenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Gonadal Dysgenesis Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Gonadal Dysgenesis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Thyroid Dysgenesis Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Thyroid Dysgenesis phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Gonadal Dysgenesis, 46,XY Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Gonadal Dysgenesis, 46,XY phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

ovarian dysgenesis 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ovarian dysgenesis 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

ovarian dysgenesis 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ovarian dysgenesis 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

ovarian dysgenesis 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ovarian dysgenesis 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

46xy partial gonadal dysgenesis, with minifascicular neuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the 46xy partial gonadal dysgenesis, with minifascicular neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

renal tubular dysgenesis Gene Set

From OMIM Gene-Disease Associations

genes associated with the renal tubular dysgenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

reticular dysgenesis Gene Set

From OMIM Gene-Disease Associations

genes associated with the reticular dysgenesis phenotype from the curated OMIM Gene-Disease Associations dataset.

globus pallidus, internal segment, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in globus pallidus, internal segment, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

globus pallidus, external segment, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in globus pallidus, external segment, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

globus pallidus, internal segment, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in globus pallidus, internal segment, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

globus pallidus, external segment, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in globus pallidus, external segment, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

Globus pallidus, internal segment Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Globus pallidus, internal segment relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Globus pallidus, external segment Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Globus pallidus, external segment relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

internal segment of globus pallidus Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in internal segment of globus pallidus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

external segment of globus pallidus Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in external segment of globus pallidus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

photoreceptor outer segment Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the photoreceptor outer segment cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

photoreceptor inner segment membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the photoreceptor inner segment membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

photoreceptor inner segment Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the photoreceptor inner segment cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

axon initial segment Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the axon initial segment cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

photoreceptor outer segment membrane Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the photoreceptor outer segment membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

photoreceptor outer segment membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the photoreceptor outer segment membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

photoreceptor outer segment Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the photoreceptor outer segment cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

photoreceptor inner segment membrane Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the photoreceptor inner segment membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

photoreceptor inner segment Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the photoreceptor inner segment cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

axon initial segment Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the axon initial segment cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

segment Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term segment in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

proximal convoluted tubule segment 2 development Gene Set

From GO Biological Process Annotations

genes participating in the proximal convoluted tubule segment 2 development biological process from the curated GO Biological Process Annotations dataset.

metanephric proximal convoluted tubule segment 2 development Gene Set

From GO Biological Process Annotations

genes participating in the metanephric proximal convoluted tubule segment 2 development biological process from the curated GO Biological Process Annotations dataset.

photoreceptor cell outer segment organization Gene Set

From GO Biological Process Annotations

genes participating in the photoreceptor cell outer segment organization biological process from the curated GO Biological Process Annotations dataset.

protein localization to photoreceptor outer segment Gene Set

From GO Biological Process Annotations

genes participating in the protein localization to photoreceptor outer segment biological process from the curated GO Biological Process Annotations dataset.

segment specification Gene Set

From GO Biological Process Annotations

genes participating in the segment specification biological process from the curated GO Biological Process Annotations dataset.

photoreceptor outer segment membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the photoreceptor outer segment membrane cellular component from the curated GO Cellular Component Annotations dataset.

photoreceptor outer segment Gene Set

From GO Cellular Component Annotations

proteins localized to the photoreceptor outer segment cellular component from the curated GO Cellular Component Annotations dataset.

photoreceptor inner segment membrane Gene Set

From GO Cellular Component Annotations

proteins localized to the photoreceptor inner segment membrane cellular component from the curated GO Cellular Component Annotations dataset.

photoreceptor inner segment Gene Set

From GO Cellular Component Annotations

proteins localized to the photoreceptor inner segment cellular component from the curated GO Cellular Component Annotations dataset.

axon initial segment Gene Set

From GO Cellular Component Annotations

proteins localized to the axon initial segment cellular component from the curated GO Cellular Component Annotations dataset.

PR segment Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the PR segment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

abnormality of the posterior segment of the eye Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the posterior segment of the eye phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

increased upper to lower segment ratio Gene Set

From HPO Gene-Disease Associations

genes associated with the increased upper to lower segment ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal st segment Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal st segment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

long-segment aganglionic megacolon Gene Set

From HPO Gene-Disease Associations

genes associated with the long-segment aganglionic megacolon phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal upper to lower segment ratio Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal upper to lower segment ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

st segment elevation Gene Set

From HPO Gene-Disease Associations

genes associated with the st segment elevation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the posterior segment of the eye Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the posterior segment of the eye phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Misato Segment II tubulin-like domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Misato Segment II tubulin-like domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Sperm equatorial segment protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Sperm equatorial segment protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

disorganized photoreceptor inner segment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the disorganized photoreceptor inner segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short photoreceptor inner segment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short photoreceptor inner segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal cone cell inner segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal cone cell inner segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short photoreceptor outer segment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short photoreceptor outer segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal rod cell outer segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal rod cell outer segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent photoreceptor outer segment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent photoreceptor outer segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

photoreceptor inner segment degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the photoreceptor inner segment degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal photoreceptor outer segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal photoreceptor outer segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal st segment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal st segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent photoreceptor inner segment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent photoreceptor inner segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

disorganized photoreceptor outer segment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the disorganized photoreceptor outer segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal loop of henle ascending limb thick segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal loop of henle ascending limb thick segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

photoreceptor outer segment degeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the photoreceptor outer segment degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal axon initial segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal axon initial segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal rod cell inner segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal rod cell inner segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal photoreceptor inner segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal photoreceptor inner segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal posterior eye segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal posterior eye segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

prolonged st segment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the prolonged st segment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal cone cell outer segment morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal cone cell outer segment morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Heterotrimeric G-protein signaling pathway-rod outer segment phototransduction Gene Set

From PANTHER Pathways

proteins participating in the Heterotrimeric G-protein signaling pathway-rod outer segment phototransduction pathway from the PANTHER Pathways dataset.

Mental retardation, anterior maxillary protrusion, and strabismus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, anterior maxillary protrusion, and strabismus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS from the curated CTD Gene-Disease Associations dataset.

Sacral defect and anterior sacral meningocele Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sacral defect and anterior sacral meningocele from the curated CTD Gene-Disease Associations dataset.

thorax and anterior abdomen determination Gene Set

From GO Biological Process Annotations

genes participating in the thorax and anterior abdomen determination biological process from the curated GO Biological Process Annotations dataset.

mental retardation, anterior maxillary protrusion, and strabismus Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, anterior maxillary protrusion, and strabismus phenotype from the curated OMIM Gene-Disease Associations dataset.

Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Set

From Reactome Pathways

proteins participating in the Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways dataset.

anterior spinal artery syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease anterior spinal artery syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

anterior compartment syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease anterior compartment syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Sacral agenesis with vertebral anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sacral agenesis with vertebral anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Testicular anomalies with or without congenital heart disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Testicular anomalies with or without congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth hormone deficiency with pituitary anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth hormone deficiency with pituitary anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anophthalmos with limb anomalies Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Anophthalmos with limb anomalies phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chondrodysplasia, acromesomelic, with genital anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Chondrodysplasia, acromesomelic, with genital anomalies from the curated CTD Gene-Disease Associations dataset.

Cavitary Optic Disc Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cavitary Optic Disc Anomalies from the curated CTD Gene-Disease Associations dataset.

Heterotopia, Periventricular, associated with Chromosome 5p Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heterotopia, Periventricular, associated with Chromosome 5p Anomalies from the curated CTD Gene-Disease Associations dataset.

Coronary Vessel Anomalies Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Coronary Vessel Anomalies from the curated CTD Gene-Disease Associations dataset.

cardiomyopathy; heart anomalies, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy; heart anomalies, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart anomalies, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart anomalies, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital anomalies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital anomalies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital anomalies; cleft lip with or without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital anomalies; cleft lip with or without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital anomalies; renal disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital anomalies; renal disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart anomalies, congenital; pulmonary hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart anomalies, congenital; pulmonary hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

thromboembolism, venous; heart anomalies, congenital; neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate; omphalocele Gene Set

From GAD Gene-Disease Associations

genes associated with the disease thromboembolism, venous; heart anomalies, congenital; neural tube defects; cleft lip with cleft palate; cleft lip without cleft palate; omphalocele in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart anomalies, congenital; cleft lip with cleft palate; cleft lip without cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart anomalies, congenital; cleft lip with cleft palate; cleft lip without cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anomalies Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term anomalies in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

pigmentation anomalies of sun-exposed skin Gene Set

From HPO Gene-Disease Associations

genes associated with the pigmentation anomalies of sun-exposed skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

multiple skeletal anomalies Gene Set

From HPO Gene-Disease Associations

genes associated with the multiple skeletal anomalies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Coronary Vessel Anomalies Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Coronary Vessel Anomalies phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

chrondrodysplasia, acromesomelic, with genital anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the chrondrodysplasia, acromesomelic, with genital anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

brain small vessel disease with or without ocular anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the brain small vessel disease with or without ocular anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

rieger or axenfeld anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the rieger or axenfeld anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

microphthalmia with limb anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the microphthalmia with limb anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

?testicular anomalies with or without congenital heart disease Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?testicular anomalies with or without congenital heart disease phenotype from the curated OMIM Gene-Disease Associations dataset.

synpolydactyly with foot anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the synpolydactyly with foot anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

cavitary optic disc anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the cavitary optic disc anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

sacral agenesis with vertebral anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the sacral agenesis with vertebral anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

growth hormone deficiency with pituitary anomalies Gene Set

From OMIM Gene-Disease Associations

genes associated with the growth hormone deficiency with pituitary anomalies phenotype from the curated OMIM Gene-Disease Associations dataset.

cleidocranial dysplasia, forme fruste, dental anomalies only Gene Set

From OMIM Gene-Disease Associations

genes associated with the cleidocranial dysplasia, forme fruste, dental anomalies only phenotype from the curated OMIM Gene-Disease Associations dataset.

Noonan syndrome and Noonan-related syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Noonan syndrome and Noonan-related syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection; wounds and injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds and injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; multiple organ failure; respiratory distress syndrome, adult; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Lynch syndrome:Lynch syndrome:Lynch syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lynch syndrome:Lynch syndrome:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

fatigue syndrome, chronic; fatigue syndrome; postviral; persian gulf syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fatigue syndrome, chronic; fatigue syndrome; postviral; persian gulf syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nocturnal myoclonus syndrome; restless legs syndrome; tourette syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nocturnal myoclonus syndrome; restless legs syndrome; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease meconium aspiration syndrome; resp distress syndrome neonatal; respiratory distress syndrome, newborn; sleep disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult; severe acute respiratory syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin resistance; metabolic syndrome x; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anterior group of nuclei, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior group of nuclei, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

anterior orbital gyrus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior orbital gyrus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral hypothalamic area, anterior region, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral hypothalamic area, anterior region, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

paracentral lobule, anterior part, right, superior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in paracentral lobule, anterior part, right, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

paracentral lobule, anterior part, right, inferior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in paracentral lobule, anterior part, right, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

paracentral lobule, anterior part, left, inferior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in paracentral lobule, anterior part, left, inferior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

paracentral lobule, anterior part, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in paracentral lobule, anterior part, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

anterior group of nuclei, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior group of nuclei, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

lateral hypothalamic area, anterior region, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral hypothalamic area, anterior region, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

paracentral lobule, anterior part, left, superior bank of gyrus Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in paracentral lobule, anterior part, left, superior bank of gyrus relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

anterior hypothalamic area, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior hypothalamic area, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

anterior orbital gyrus, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior orbital gyrus, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

anterior hypothalamic area, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior hypothalamic area, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

anterior olfactory area, dorsal part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior olfactory area, dorsal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

anterior olfactory area, ventral part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior olfactory area, ventral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

anterior tegmental nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior tegmental nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior cingulate area, ventral part, layer 2/3 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior cingulate area, ventral part, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior cingulate area, dorsal part, layer 5 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior cingulate area, dorsal part, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

nucleus of the stria terminalis, medial division, anterior part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in nucleus of the stria terminalis, medial division, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

anterior paraventricular nucleus of thalamus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior paraventricular nucleus of thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Bed nuclei of the stria terminalis, anterior division, anterolateral area Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, anterolateral area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Bed nuclei of the stria terminalis, anterior division Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Bed nuclei of the stria terminalis, anterior division relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

anterior pretectal nucleus, ventral core part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior pretectal nucleus, ventral core part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Bed nuclei of the stria terminalis, anterior division, oval nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, oval nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

anterior nuclei Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior nuclei relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Dorsomedial nucleus of the hypothalamus, anterior part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Dorsomedial nucleus of the hypothalamus, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior olfactory nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior olfactory nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

anterior digastric muscle trigeminal motor cell group Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior digastric muscle trigeminal motor cell group relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior cingulate area Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior cingulate area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

interstitial nucleus of the posterior limb of the anterior commissure Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in interstitial nucleus of the posterior limb of the anterior commissure relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior cingulate area, ventral part, layer 5 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior cingulate area, ventral part, layer 5 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior cingulate area, ventral part, layer 1 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior cingulate area, ventral part, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior cingulate area, dorsal part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior cingulate area, dorsal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Bed nuclei of the stria terminalis, anterior division, fusiform nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, fusiform nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Bed nuclei of the stria terminalis, anterior division, ventral nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, ventral nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior hypothalamic nucleus, central part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior hypothalamic nucleus, central part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Bed nuclei of the stria terminalis, anterior division, juxtacapsular nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, juxtacapsular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Bed nuclei of the stria terminalis, anterior division, anteromedial area Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, anteromedial area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Basolateral amygdalar nucleus, anterior part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Basolateral amygdalar nucleus, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

anterior pretectal nucleus, ventral superficial part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior pretectal nucleus, ventral superficial part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Bed nucleus of the anterior commissure Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Bed nucleus of the anterior commissure relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior group of the dorsal thalamus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior group of the dorsal thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

anterior pretectal nucleus, dorsal superficial part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior pretectal nucleus, dorsal superficial part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior olfactory nucleus, lateral part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior olfactory nucleus, lateral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

anterior pretectal nucleus, dorsal core part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior pretectal nucleus, dorsal core part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

basomedial amygdaloid nucleus, anterior part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in basomedial amygdaloid nucleus, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Paraventricular hypothalamic nucleus, parvicellular division, anterior parvicellular part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Paraventricular hypothalamic nucleus, parvicellular division, anterior parvicellular part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Ventral anterior-lateral complex of the thalamus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Ventral anterior-lateral complex of the thalamus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior amygdalar area Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior amygdalar area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior olfactory nucleus, dorsal part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior olfactory nucleus, dorsal part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior cingulate area, dorsal part, layer 2/3 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior cingulate area, dorsal part, layer 2/3 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior olfactory nucleus, external part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior olfactory nucleus, external part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Cortical amygdalar area, anterior part, layer 2 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Cortical amygdalar area, anterior part, layer 2 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior olfactory nucleus, medial part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior olfactory nucleus, medial part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Bed nuclei of the stria terminalis, anterior division, rhomboid nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, rhomboid nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior cingulate area, dorsal part, layer 1 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior cingulate area, dorsal part, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

basolateral amygdaloid nucleus, anterior part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in basolateral amygdaloid nucleus, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior hypothalamic nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Cortical amygdalar area, anterior part, layer 1 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Cortical amygdalar area, anterior part, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Basomedial amygdalar nucleus, anterior part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Basomedial amygdalar nucleus, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior olfactory nucleus, posteroventral part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior olfactory nucleus, posteroventral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

anterior part of Int Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior part of Int relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior hypothalamic nucleus, posterior part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior hypothalamic nucleus, posterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior cingulate area, ventral part, 6b Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior cingulate area, ventral part, 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior cingulate area, ventral part, 6a Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior cingulate area, ventral part, 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Bed nuclei of the stria terminalis, anterior division, magnocellular nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, magnocellular nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Cortical amygdalar area, anterior part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Cortical amygdalar area, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior cingulate area, ventral part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior cingulate area, ventral part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior olfactory nucleus, layer 1 Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior olfactory nucleus, layer 1 relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior pretectal nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior pretectal nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior cingulate area, dorsal part, layer 6b Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior cingulate area, dorsal part, layer 6b relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Anterior cingulate area, dorsal part, layer 6a Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Anterior cingulate area, dorsal part, layer 6a relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Bed nuclei of the stria terminalis, anterior division, dorsomedial nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Bed nuclei of the stria terminalis, anterior division, dorsomedial nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

posterior part of anterior hypothalamic nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in posterior part of anterior hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

lateral anterior hypothalamic nucleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral anterior hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Ventromedial hypothalamic nucleus, anterior part Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Ventromedial hypothalamic nucleus, anterior part relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

anterior cortical amygdaloid area Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior cortical amygdaloid area relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_15 yrs_M_12299 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_15 yrs_M_12299 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_M_12820 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12879 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_3 yrs_M_12980 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_23 yrs_M_12300 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_37 yrs_M_12303 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_36 yrs_M_12302 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_8 yrs_M_12841 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_10 mos_M_12977 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_9 pcw_M_12833 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_9 pcw_M_12833 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_21 pcw_M_12886 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_12960 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_12960 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_21 pcw_F_12365 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_21 pcw_F_12365 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_17 pcw_F_12880 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_1 yrs_F_12830 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_13060 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_30 yrs_F_12290 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_2 yrs_F_12979 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_13 yrs_F_12831 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_18 yrs_M_12984 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_21 yrs_F_13057 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_8 pcw_M_13058 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_12835 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_40 yrs_F_12304 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_40 yrs_F_12304 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_19 pcw_F_12885 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_24 pcw_M_12288 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_4 mos_M_12296 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_F_12834 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12837 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_4 yrs_M_12298 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_4 yrs_M_12298 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12287 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_M_12888 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_M_12820 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_M_12820 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12879 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12879 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_19 yrs_F_12832 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_19 yrs_F_12832 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_19 pcw_F_12885 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_19 pcw_F_12885 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_8 yrs_M_12981 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_8 yrs_M_12981 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_3 yrs_M_12980 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_3 yrs_M_12980 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_37 yrs_M_12303 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_37 yrs_M_12303 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_36 yrs_M_12302 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_36 yrs_M_12302 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_11 yrs_F_12289 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_11 yrs_F_12289 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_8 yrs_M_12841 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_8 yrs_M_12841 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_10 mos_M_12977 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_10 mos_M_12977 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_9 pcw_M_12833 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_9 pcw_M_12833 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_17 pcw_F_12880 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_17 pcw_F_12880 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_21 pcw_M_12886 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_21 pcw_M_12886 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_13060 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_13060 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_1 yrs_F_12830 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_1 yrs_F_12830 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_37 pcw_M_263195015 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_37 pcw_M_263195015 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_30 yrs_F_12290 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_30 yrs_F_12290 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_2 yrs_F_12979 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_2 yrs_F_12979 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_13 yrs_F_12831 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_13 yrs_F_12831 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_18 yrs_M_12984 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_18 yrs_M_12984 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_12835 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_12 pcw_F_12835 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_21 yrs_F_13057 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_21 yrs_F_13057 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_4 mos_M_12890 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_4 mos_M_12890 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_8 pcw_M_13058 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_8 pcw_M_13058 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_M_12888 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_M_12888 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_24 pcw_M_12288 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_24 pcw_M_12288 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_4 mos_M_12296 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_4 mos_M_12296 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_F_12834 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_13 pcw_F_12834 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12837 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12837 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12287 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_16 pcw_M_12287 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior (rostral) cingulate (medial prefrontal) cortex_23 yrs_M_12300 Gene Set

From Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq

genes with high or low expression in anterior (rostral) cingulate (medial prefrontal) cortex_23 yrs_M_12300 relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.

anterior hypothalamic nucleus Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior hypothalamic nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

anterior nucleus of pulvinar Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior nucleus of pulvinar relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

anterior cortical nucleus Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior cortical nucleus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

ventral anterior nucleus of thalamus Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in ventral anterior nucleus of thalamus relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

anterior amygdaloid area Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in anterior amygdaloid area relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

lateral hypothalamic area, anterior part Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in lateral hypothalamic area, anterior part relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

rostral (anterior) extramural migratory stream Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in rostral (anterior) extramural migratory stream relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

Lethal arthrogryposis with anterior horn cell disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lethal arthrogryposis with anterior horn cell disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NONARTERITIC ANTERIOR ISCHEMIC OPTIC NEUROPATHY, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

Myopathy, Distal, with Anterior Tibial Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Distal, with Anterior Tibial Onset from the curated CTD Gene-Disease Associations dataset.

Anterior polar cataract 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anterior polar cataract 2 from the curated CTD Gene-Disease Associations dataset.

Lethal Arthrogryposis With Anterior Horn Cell Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lethal Arthrogryposis With Anterior Horn Cell Disease from the curated CTD Gene-Disease Associations dataset.

anterior horn cell disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease anterior horn cell disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

anterior cranial fossa meningioma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease anterior cranial fossa meningioma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

anterior uveitis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease anterior uveitis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

anterior scleritis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease anterior scleritis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

anterior cerebral artery infarction Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease anterior cerebral artery infarction in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

anterior ischemic optic neuropathy Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease anterior ischemic optic neuropathy in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

rheumatoid spondylitis; spondylitis, ankylosing; uveitis, anterior Gene Set

From GAD Gene-Disease Associations

genes associated with the disease rheumatoid spondylitis; spondylitis, ankylosing; uveitis, anterior in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

uveitis, anterior Gene Set

From GAD Gene-Disease Associations

genes associated with the disease uveitis, anterior in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute anterior uveitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute anterior uveitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anterior wall myocardial infarction; arrhythmias, cardiac; death, sudden, cardiac; disease susceptibility; heart arrest; myocardial infarction; sudden cardiac death; ventricular fibrillation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anterior wall myocardial infarction; arrhythmias, cardiac; death, sudden, cardiac; disease susceptibility; heart arrest; myocardial infarction; sudden cardiac death; ventricular fibrillation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anterior Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term anterior in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

H6PD_KO_GDS3195_603_mouse_Skeletal muscle - Tibialis anterior Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the H6PD_KO_GDS3195_603_mouse_Skeletal muscle - Tibialis anterior gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

positive regulation of anterior head development Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of anterior head development biological process from the curated GO Biological Process Annotations dataset.

embryonic heart tube anterior/posterior pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the embryonic heart tube anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations dataset.

anterior/posterior axis specification, embryo Gene Set

From GO Biological Process Annotations

genes participating in the anterior/posterior axis specification, embryo biological process from the curated GO Biological Process Annotations dataset.

specification of ureteric bud anterior/posterior symmetry Gene Set

From GO Biological Process Annotations

genes participating in the specification of ureteric bud anterior/posterior symmetry biological process from the curated GO Biological Process Annotations dataset.

anterior neuropore closure Gene Set

From GO Biological Process Annotations

genes participating in the anterior neuropore closure biological process from the curated GO Biological Process Annotations dataset.

anterior compartment pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the anterior compartment pattern formation biological process from the curated GO Biological Process Annotations dataset.

cardioblast anterior-lateral migration Gene Set

From GO Biological Process Annotations

genes participating in the cardioblast anterior-lateral migration biological process from the curated GO Biological Process Annotations dataset.

negative regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

anterior/posterior pattern specification involved in kidney development Gene Set

From GO Biological Process Annotations

genes participating in the anterior/posterior pattern specification involved in kidney development biological process from the curated GO Biological Process Annotations dataset.

canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

anterior commissure morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the anterior commissure morphogenesis biological process from the curated GO Biological Process Annotations dataset.

anterior/posterior pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations dataset.

polarity specification of anterior/posterior axis Gene Set

From GO Biological Process Annotations

genes participating in the polarity specification of anterior/posterior axis biological process from the curated GO Biological Process Annotations dataset.

specification of anterior mesonephric tubule identity Gene Set

From GO Biological Process Annotations

genes participating in the specification of anterior mesonephric tubule identity biological process from the curated GO Biological Process Annotations dataset.

epiblast cell-extraembryonic ectoderm cell signaling involved in anterior/posterior axis specification Gene Set

From GO Biological Process Annotations

genes participating in the epiblast cell-extraembryonic ectoderm cell signaling involved in anterior/posterior axis specification biological process from the curated GO Biological Process Annotations dataset.

spemann organizer formation at the anterior end of the primitive streak Gene Set

From GO Biological Process Annotations

genes participating in the spemann organizer formation at the anterior end of the primitive streak biological process from the curated GO Biological Process Annotations dataset.

zygotic determination of anterior/posterior axis, embryo Gene Set

From GO Biological Process Annotations

genes participating in the zygotic determination of anterior/posterior axis, embryo biological process from the curated GO Biological Process Annotations dataset.

regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

anterior/posterior axis specification Gene Set

From GO Biological Process Annotations

genes participating in the anterior/posterior axis specification biological process from the curated GO Biological Process Annotations dataset.

fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the fibroblast growth factor receptor signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

neural plate anterior/posterior regionalization Gene Set

From GO Biological Process Annotations

genes participating in the neural plate anterior/posterior regionalization biological process from the curated GO Biological Process Annotations dataset.

spinal cord anterior/posterior patterning Gene Set

From GO Biological Process Annotations

genes participating in the spinal cord anterior/posterior patterning biological process from the curated GO Biological Process Annotations dataset.

anterior/posterior axon guidance Gene Set

From GO Biological Process Annotations

genes participating in the anterior/posterior axon guidance biological process from the curated GO Biological Process Annotations dataset.

regulation of anterior head development Gene Set

From GO Biological Process Annotations

genes participating in the regulation of anterior head development biological process from the curated GO Biological Process Annotations dataset.

anterior/posterior pattern specification involved in ureteric bud development Gene Set

From GO Biological Process Annotations

genes participating in the anterior/posterior pattern specification involved in ureteric bud development biological process from the curated GO Biological Process Annotations dataset.

anterior semicircular canal development Gene Set

From GO Biological Process Annotations

genes participating in the anterior semicircular canal development biological process from the curated GO Biological Process Annotations dataset.

regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of canonical wnt signaling pathway involved in neural plate anterior/posterior pattern formation biological process from the curated GO Biological Process Annotations dataset.

forebrain anterior/posterior pattern specification Gene Set

From GO Biological Process Annotations

genes participating in the forebrain anterior/posterior pattern specification biological process from the curated GO Biological Process Annotations dataset.

specification of ureteric bud anterior/posterior symmetry by bmp signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the specification of ureteric bud anterior/posterior symmetry by bmp signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of transcription involved in anterior/posterior axis specification Gene Set

From GO Biological Process Annotations

genes participating in the regulation of transcription involved in anterior/posterior axis specification biological process from the curated GO Biological Process Annotations dataset.

Anterior chamber depth Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Anterior chamber depth phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

abnormality of the anterior pituitary Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the anterior pituitary phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

anterior polar cataract Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior polar cataract phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior chamber synechiae Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior chamber synechiae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

irregular ossification at anterior rib ends Gene Set

From HPO Gene-Disease Associations

genes associated with the irregular ossification at anterior rib ends phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior beaking of lumbar vertebrae Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior beaking of lumbar vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior encephalocele Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior encephalocele phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the anterior chamber Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the anterior chamber phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

left anterior fascicular block Gene Set

From HPO Gene-Disease Associations

genes associated with the left anterior fascicular block phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior tibial bowing Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior tibial bowing phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior beaking of thoracic vertebrae Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior beaking of thoracic vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior rib cupping Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior rib cupping phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

small anterior fontanelle Gene Set

From HPO Gene-Disease Associations

genes associated with the small anterior fontanelle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

wide anterior fontanel Gene Set

From HPO Gene-Disease Associations

genes associated with the wide anterior fontanel phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

thick anterior alveolar ridges Gene Set

From HPO Gene-Disease Associations

genes associated with the thick anterior alveolar ridges phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior sacral meningocele Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior sacral meningocele phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior clefting of vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior clefting of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior hypopituitarism Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior hypopituitarism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

deep anterior chamber Gene Set

From HPO Gene-Disease Associations

genes associated with the deep anterior chamber phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior creases of earlobe Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior creases of earlobe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

polymicrogyria, anterior to posterior gradient Gene Set

From HPO Gene-Disease Associations

genes associated with the polymicrogyria, anterior to posterior gradient phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

low anterior hairline Gene Set

From HPO Gene-Disease Associations

genes associated with the low anterior hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the anterior fontanelle Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the anterior fontanelle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior open-bite malocclusion Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior open-bite malocclusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

neoplasm of the anterior pituitary Gene Set

From HPO Gene-Disease Associations

genes associated with the neoplasm of the anterior pituitary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior open bite Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior open bite phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior basal encephalocele Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior basal encephalocele phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior beaking of lower thoracic vertebrae Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior beaking of lower thoracic vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

midline skin dimples over anterior/posterior fontanelles Gene Set

From HPO Gene-Disease Associations

genes associated with the midline skin dimples over anterior/posterior fontanelles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal anterior horn cell morphology Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal anterior horn cell morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

delayed closure of the anterior fontanelle Gene Set

From HPO Gene-Disease Associations

genes associated with the delayed closure of the anterior fontanelle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

nonarteritic anterior ischemic optic neuropathy Gene Set

From HPO Gene-Disease Associations

genes associated with the nonarteritic anterior ischemic optic neuropathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

persistent open anterior fontanelle Gene Set

From HPO Gene-Disease Associations

genes associated with the persistent open anterior fontanelle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of the anterior pituitary Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the anterior pituitary phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

paucity of anterior horn motor neurons Gene Set

From HPO Gene-Disease Associations

genes associated with the paucity of anterior horn motor neurons phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior bowing of long bones Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior bowing of long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior lenticonus Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior lenticonus phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior wedging of l2 Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior wedging of l2 phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior wedging of l1 Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior wedging of l1 phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior rounding of vertebral bodies Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior rounding of vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

disorganization of the anterior cerebellar vermis Gene Set

From HPO Gene-Disease Associations

genes associated with the disorganization of the anterior cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

shallow anterior chamber Gene Set

From HPO Gene-Disease Associations

genes associated with the shallow anterior chamber phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

high anterior hairline Gene Set

From HPO Gene-Disease Associations

genes associated with the high anterior hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior rib punctate calcifications Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior rib punctate calcifications phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior pituitary agenesis Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior pituitary agenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior pituitary hypoplasia Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior pituitary hypoplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior radial head dislocation Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior radial head dislocation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

degeneration of anterior horn cells Gene Set

From HPO Gene-Disease Associations

genes associated with the degeneration of anterior horn cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

anterior concavity of thoracic vertebrae Gene Set

From HPO Gene-Disease Associations

genes associated with the anterior concavity of thoracic vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent anterior eye chamber Gene Set

From HPO Gene-Disease Associations

genes associated with the absent anterior eye chamber phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Anterior Wall Myocardial Infarction Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Anterior Wall Myocardial Infarction phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Infarction, Anterior Cerebral Artery Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Infarction, Anterior Cerebral Artery phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Uveitis, Anterior Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Uveitis, Anterior phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

absent anterior definitive endoderm Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent anterior definitive endoderm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal anterior commissure morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal anterior commissure morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

anterior subcapsular cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the anterior subcapsular cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

anterior polar cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the anterior polar cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased anterior commissure size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased anterior commissure size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal anterior lingual gland morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal anterior lingual gland morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased tibialis anterior weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased tibialis anterior weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal anterior visceral endoderm morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal anterior visceral endoderm morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal medulla oblongata anterior median fissure morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal medulla oblongata anterior median fissure morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cerebellum anterior vermis morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cerebellum anterior vermis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent anterior lingual gland Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent anterior lingual gland phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent arcus anterior Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent arcus anterior phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

prostate gland anterior lobe hyperplasia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the prostate gland anterior lobe hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal eye anterior chamber morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal eye anterior chamber morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

enlarged eye anterior chamber Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the enlarged eye anterior chamber phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent prostate gland anterior lobe Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent prostate gland anterior lobe phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

anterior iris synechia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the anterior iris synechia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cerebellum anterior lobe morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cerebellum anterior lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal anterior visceral endoderm cell migration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal anterior visceral endoderm cell migration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased anterior commissure size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased anterior commissure size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal eye anterior chamber depth Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal eye anterior chamber depth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal anterior primitive streak morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal anterior primitive streak morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent anterior visceral endoderm Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent anterior visceral endoderm phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal anterior corticospinal tract morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal anterior corticospinal tract morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal anterior definitive endoderm morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal anterior definitive endoderm morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

enlarged prostate gland anterior lobe Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the enlarged prostate gland anterior lobe phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal anterior commissure pars posterior morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal anterior commissure pars posterior morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal arcus anterior morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal arcus anterior morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal tibialis anterior weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal tibialis anterior weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal tibialis anterior morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal tibialis anterior morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

large anterior fontanelle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the large anterior fontanelle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased anterior vermis size Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased anterior vermis size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

small prostate gland anterior lobe Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the small prostate gland anterior lobe phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal anterior stroma morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal anterior stroma morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent anterior chamber Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent anterior chamber phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

anterior cortical cataracts Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the anterior cortical cataracts phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal prostate gland anterior lobe morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal prostate gland anterior lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal anterior uvea morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal anterior uvea morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased tibialis anterior weight Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased tibialis anterior weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal anterior cardinal vein morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal anterior cardinal vein morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent anterior commissure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent anterior commissure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

arthrogryposis, lethal, with anterior horn cell disease Gene Set

From OMIM Gene-Disease Associations

genes associated with the arthrogryposis, lethal, with anterior horn cell disease phenotype from the curated OMIM Gene-Disease Associations dataset.

{nonarteritic anterior ischemic optic neuropathy, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {nonarteritic anterior ischemic optic neuropathy, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, distal, with anterior tibial onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, distal, with anterior tibial onset phenotype from the curated OMIM Gene-Disease Associations dataset.

H3K36me3_Brain Anterior Caudate Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K36me3_Brain Anterior Caudate histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K9ac_Brain Anterior Caudate Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K9ac_Brain Anterior Caudate histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K9me3_Brain Anterior Caudate Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K9me3_Brain Anterior Caudate histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K4me3_Brain Anterior Caudate Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me3_Brain Anterior Caudate histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K27me3_Brain Anterior Caudate Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K27me3_Brain Anterior Caudate histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K4me1_Brain Anterior Caudate Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K4me1_Brain Anterior Caudate histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

H3K27ac_Brain Anterior Caudate Gene Set

From Roadmap Epigenomics Histone Modification Site Profiles

genes with high histone modification abundance in the H3K27ac_Brain Anterior Caudate histone modification site profile from the Roadmap Epigenomics Histone Modification Site Profiles dataset.

anterior lobe Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

proteins highly expressed in the tissue anterior lobe from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset.

anterior visceral endoderm Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue anterior visceral endoderm in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

anterior commissure Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue anterior commissure in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

anterior chamber of the eye Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue anterior chamber of the eye in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

anterior paraventricular nucleus Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue anterior paraventricular nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

ventral anterior nucleus of thalamus Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue ventral anterior nucleus of thalamus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

anterior adductor muscle Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue anterior adductor muscle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

anterior visceral ectoderm Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue anterior visceral ectoderm in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

anterior spinal root Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue anterior spinal root in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

tibialis anterior Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue tibialis anterior in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

anterior silk gland Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue anterior silk gland in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

anterior midgut Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue anterior midgut in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

anterior cingulate cortex Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue anterior cingulate cortex in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

anterior cardinal vein Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue anterior cardinal vein in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

anterior olfactory lobule Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue anterior olfactory lobule in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

anterior hypothalamic nucleus Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue anterior hypothalamic nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

anterior lobe Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue anterior lobe in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

anterior pharynx Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue anterior pharynx in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

anterior olfactory nucleus Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue anterior olfactory nucleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

anterior horn Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue anterior horn in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression Gene Set

From Biocarta Pathways

proteins participating in the basic mechanism of action of ppara pparb(d) and pparg and effects on gene expression pathway from the Biocarta Pathways dataset.

BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BRCA1 and BRCA2 Hereditary Breast and Ovarian Cancer phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Coloboma, uveal, with cleft lip and palate and mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Coloboma, uveal, with cleft lip and palate and mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, progressive, with seizures and cerebral and cerebellar atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diabetes mellitus AND insipidus with optic atrophy AND deafness Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diabetes mellitus AND insipidus with optic atrophy AND deafness phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset.

Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leukoencephalopathy with Brainstem and Spinal Cord Involvement and Lactate Elevation from the curated CTD Gene-Disease Associations dataset.

Congenital, Hereditary, and Neonatal Diseases and Abnormalities Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities from the curated CTD Gene-Disease Associations dataset.

Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation And Microcephaly With Pontine And Cerebellar Hypoplasia from the curated CTD Gene-Disease Associations dataset.

Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, Hereditary Sensory And Autonomic, Type I, With Cough And Gastroesophageal Reflux from the curated CTD Gene-Disease Associations dataset.

Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations from the curated CTD Gene-Disease Associations dataset.

postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anxiety and hostility and depression Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anxiety and hostility and depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease charcot-marie-tooth disease; hereditary motor and sensory neuropathies; hereditary sensory and motor neuropathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

frontotemporal dementia and pick-like 3r and 4r tauopathy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease frontotemporal dementia and pick-like 3r and 4r tauopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

squamous cell carcinomas of the head and neck (scchn) and breast cancer Gene Set

From GAD Gene-Disease Associations

genes associated with the disease squamous cell carcinomas of the head and neck (scchn) and breast cancer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

vitamins and metabolites in pregnant women and neonates Gene Set

From GAD Gene-Disease Associations

genes associated with the disease vitamins and metabolites in pregnant women and neonates in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

racemase and epimerase activity, acting on amino acids and derivatives Gene Set

From GO Molecular Function Annotations

genes performing the racemase and epimerase activity, acting on amino acids and derivatives molecular function from the curated GO Molecular Function Annotations dataset.

racemase and epimerase activity, acting on carbohydrates and derivatives Gene Set

From GO Molecular Function Annotations

genes performing the racemase and epimerase activity, acting on carbohydrates and derivatives molecular function from the curated GO Molecular Function Annotations dataset.

leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation Gene Set

From OMIM Gene-Disease Associations

genes associated with the leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation phenotype from the curated OMIM Gene-Disease Associations dataset.

microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma Gene Set

From OMIM Gene-Disease Associations

genes associated with the microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma phenotype from the curated OMIM Gene-Disease Associations dataset.

hypomyelination with brainstem and spinal cord involvement and leg spasticity Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypomyelination with brainstem and spinal cord involvement and leg spasticity phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, mental retardation, and distinctive facies, with cardiac and genitourinary malformations phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation and microcephaly with pontine and cerebellar hypoplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation and microcephaly with pontine and cerebellar hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, progressive, seizures, and cerebral and cerebellar atrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, progressive, seizures, and cerebral and cerebellar atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Gene Set

From Reactome Pathways

proteins participating in the Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S pathway from the Reactome Pathways dataset.

Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding Gene Set

From Reactome Pathways

proteins participating in the Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding pathway from the Reactome Pathways dataset.

PI and PC transport between ER and Golgi membranes Gene Set

From Reactome Pathways

proteins participating in the PI and PC transport between ER and Golgi membranes pathway from the Reactome Pathways dataset.

Orexin and neuropeptides FF and QRFP bind to their respective receptors Gene Set

From Reactome Pathways

proteins participating in the Orexin and neuropeptides FF and QRFP bind to their respective receptors pathway from the Reactome Pathways dataset.

FGFR1c and Klotho ligand binding and activation Gene Set

From Reactome Pathways

proteins participating in the FGFR1c and Klotho ligand binding and activation pathway from the Reactome Pathways dataset.

Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane Gene Set

From Reactome Pathways

proteins participating in the Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane pathway from the Reactome Pathways dataset.

Synthesis and processing of ENV and VPU Gene Set

From Reactome Pathways

proteins participating in the Synthesis and processing of ENV and VPU pathway from the Reactome Pathways dataset.

Synthesis and interconversion of nucleotide di- and triphosphates Gene Set

From Reactome Pathways

proteins participating in the Synthesis and interconversion of nucleotide di- and triphosphates pathway from the Reactome Pathways dataset.

SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) pathway from the Wikipathways Pathways dataset.

SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) pathway from the Wikipathways Pathways dataset.

SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the SRF and miRs in Smooth Muscle Differentiation and Proliferation(Homo sapiens) pathway from the Wikipathways Pathways dataset.

visceral fat deposits and the metabolic syndrome Gene Set

From Biocarta Pathways

proteins participating in the visceral fat deposits and the metabolic syndrome pathway from the Biocarta Pathways dataset.

Retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Foveal hypoplasia and presenile cataract syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Foveal hypoplasia and presenile cataract syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Rigidity and multifocal seizure syndrome, lethal neonatal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alopecia, neurologic defects, and endocrinopathy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Knuckle pads, deafness AND leukonychia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Knuckle pads, deafness AND leukonychia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Jervell and Lange-Nielsen syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Jervell and Lange-Nielsen syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, epilepsy, and diabetes syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, epilepsy, and diabetes syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, hiatal hernia and nephrotic syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, hiatal hernia and nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Jervell and Lange-Nielsen syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Jervell and Lange-Nielsen syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cutis Gyrata syndrome of Beare and Stevenson Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cutis Gyrata syndrome of Beare and Stevenson phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alacrima, achalasia, and mental retardation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alacrima, achalasia, and mental retardation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cutaneous telangiectasia and cancer syndrome, familial Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pineal hyperplasia AND diabetes mellitus syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pineal hyperplasia AND diabetes mellitus syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Camptodactyly, tall stature, and hearing loss syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Camptodactyly, tall stature, and hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal dystrophy, iris coloboma, and comedogenic acne syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, and Hirschsprung Disease from the curated CTD Gene-Disease Associations dataset.

Keratitis, Ichthyosis, and Deafness (KID) Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Keratitis, Ichthyosis, and Deafness (KID) Syndrome from the curated CTD Gene-Disease Associations dataset.

Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 3 from the curated CTD Gene-Disease Associations dataset.

Cutis Gyrata Syndrome of Beare And Stevenson Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cutis Gyrata Syndrome of Beare And Stevenson from the curated CTD Gene-Disease Associations dataset.

Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 from the curated CTD Gene-Disease Associations dataset.

Hereditary Breast and Ovarian Cancer Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hereditary Breast and Ovarian Cancer Syndrome from the curated CTD Gene-Disease Associations dataset.

Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 from the curated CTD Gene-Disease Associations dataset.

Sarcoma family syndrome of Li and Fraumeni Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sarcoma family syndrome of Li and Fraumeni from the curated CTD Gene-Disease Associations dataset.

Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis from the curated CTD Gene-Disease Associations dataset.

Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 from the curated CTD Gene-Disease Associations dataset.

Jervell And Lange-Nielsen Syndrome 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Jervell And Lange-Nielsen Syndrome 2 from the curated CTD Gene-Disease Associations dataset.

Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alopecia, Neurologic Defects, and Endocrinopathy Syndrome from the curated CTD Gene-Disease Associations dataset.

Renal cysts and diabetes syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Renal cysts and diabetes syndrome from the curated CTD Gene-Disease Associations dataset.

blepharophimosis, ptosis, and epicanthus inversus syndrome Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease blepharophimosis, ptosis, and epicanthus inversus syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

tooth and nail syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease tooth and nail syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

blepharophimosis, ptosis, and epicanthus inversus syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease blepharophimosis, ptosis, and epicanthus inversus syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

hyper-ige syndrome and severe eczema. atopy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyper-ige syndrome and severe eczema. atopy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

psoriasis, psoriatic arthritis, and sapho syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease psoriasis, psoriatic arthritis, and sapho syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

jervell and lange-nielsen syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease jervell and lange-nielsen syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyper-igm syndrome can form oligomers and trigger cd40-mediated signals Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyper-igm syndrome can form oligomers and trigger cd40-mediated signals in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leigh syndrome and cytochrome c oxidase deficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leigh syndrome and cytochrome c oxidase deficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

complete androgen insensitivity syndrome and sertoli cell adenoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complete androgen insensitivity syndrome and sertoli cell adenoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

metabolic syndrome and electrocardiographic coronary artery disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease metabolic syndrome and electrocardiographic coronary artery disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

critical illness; respiratory distress syndrome, adult; wounds and injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease critical illness; respiratory distress syndrome, adult; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

systemic inflammatory response syndrome; wounds and injuries Gene Set

From GAD Gene-Disease Associations

genes associated with the disease systemic inflammatory response syndrome; wounds and injuries in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

elevated liver enzymes and metabolic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease elevated liver enzymes and metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

prader-willi and angelman syndromes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease prader-willi and angelman syndromes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

tic; combined vocal and multiple motor; tourette syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease tic; combined vocal and multiple motor; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

li-fraumeni and related syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease li-fraumeni and related syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Stevens-Johnson syndrome and toxic epidermal necrolysis (SJS-TEN) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Stevens-Johnson syndrome and toxic epidermal necrolysis (SJS-TEN) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

myasthenic syndrome, congenital, associated with facial dysmorphism and acetylcholine receptor deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenic syndrome, congenital, associated with facial dysmorphism and acetylcholine receptor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

jervell and lange-nielsen syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the jervell and lange-nielsen syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

lymphedema-distichiasis syndrome with renal disease and diabetes mellitus Gene Set

From OMIM Gene-Disease Associations

genes associated with the lymphedema-distichiasis syndrome with renal disease and diabetes mellitus phenotype from the curated OMIM Gene-Disease Associations dataset.

melanoma and neural system tumor syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the melanoma and neural system tumor syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

renal cysts and diabetes syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the renal cysts and diabetes syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

alacrima, achalasia, and mental retardation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the alacrima, achalasia, and mental retardation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

rigidity and multifocal seizure syndrome, lethal neonatal Gene Set

From OMIM Gene-Disease Associations

genes associated with the rigidity and multifocal seizure syndrome, lethal neonatal phenotype from the curated OMIM Gene-Disease Associations dataset.

myelodysplasia and leukemia syndrome with monosomy 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the myelodysplasia and leukemia syndrome with monosomy 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

aicardi-goutieres syndrome 1, dominant and recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the aicardi-goutieres syndrome 1, dominant and recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

?cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

proliferative vasculopathy and hydraencephaly-hydrocephaly syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the proliferative vasculopathy and hydraencephaly-hydrocephaly syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

?retinal dystrophy, juvenile cataracts, and short stature syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?retinal dystrophy, juvenile cataracts, and short stature syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

retinol dystrophy, iris coloboma, and comedogenic acne syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinol dystrophy, iris coloboma, and comedogenic acne syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene Set

From OMIM Gene-Disease Associations

genes associated with the interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, epilepsy, and diabetes syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, epilepsy, and diabetes syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

3-methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the 3-methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

jervell and lange-nielsen syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the jervell and lange-nielsen syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated OMIM Gene-Disease Associations dataset.

autoinflammation, antibody deficiency, and immune dysregulation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoinflammation, antibody deficiency, and immune dysregulation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

alopecia, neurologic defects, and endocrinopathy syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the alopecia, neurologic defects, and endocrinopathy syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

cutaneous telangiectasia and cancer syndrome, familial Gene Set

From OMIM Gene-Disease Associations

genes associated with the cutaneous telangiectasia and cancer syndrome, familial phenotype from the curated OMIM Gene-Disease Associations dataset.

mitochondrial recessive ataxia syndrome (includes sando and scae) Gene Set

From OMIM Gene-Disease Associations

genes associated with the mitochondrial recessive ataxia syndrome (includes sando and scae) phenotype from the curated OMIM Gene-Disease Associations dataset.

autoinflammation, lipodystrophy, and dermatosis syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the autoinflammation, lipodystrophy, and dermatosis syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis phenotype from the curated OMIM Gene-Disease Associations dataset.

?partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Lynch syndrome:Turcot syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lynch syndrome:Turcot syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary cancer-predisposing syndrome:Lynch syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary cancer-predisposing syndrome:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Zunich neuroectodermal syndrome:Zunich neuroectodermal syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Zunich neuroectodermal syndrome:Zunich neuroectodermal syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Von Hippel-Lindau syndrome:Hereditary cancer-predisposing syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Von Hippel-Lindau syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lynch syndrome:Hereditary cancer-predisposing syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lynch syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lynch syndrome:Lynch syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lynch syndrome:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Marfan's syndrome:Marfan's syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Marfan's syndrome:Marfan's syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary cancer-predisposing syndrome:Peutz-Jeghers syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary cancer-predisposing syndrome:Peutz-Jeghers syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

IFAP syndrome with or without BRESHECK syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the IFAP syndrome with or without BRESHECK syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lynch syndrome I:Lynch syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lynch syndrome I:Lynch syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hereditary cancer-predisposing syndrome:Hereditary cancer-predisposing syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary cancer-predisposing syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Miller-McKusick-Malvaux-Syndrome (3M Syndrome) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Miller-McKusick-Malvaux-Syndrome (3M Syndrome) from the curated CTD Gene-Disease Associations dataset.

Digeorge Syndrome/Velocardiofacial Syndrome Complex 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Digeorge Syndrome/Velocardiofacial Syndrome Complex 2 from the curated CTD Gene-Disease Associations dataset.

menarch; natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious Gene Set

From GAD Gene-Disease Associations

genes associated with the disease menarch; natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperhomocysteinemia; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperhomocysteinemia; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cornelia de lange syndrome; de lange syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cornelia de lange syndrome; de lange syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fatigue syndrome, chronic; fatigue syndrome; postviral Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fatigue syndrome, chronic; fatigue syndrome; postviral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease resp distress syndrome neonatal; respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lung diseases; resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lung diseases; resp distress syndrome neonatal; respiratory distress syndrome, newborn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperandrogenism; insulin resistance; obesity; polycystic ovarian syndrome; polycystic ovary syndrome; thinness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperandrogenism; insulin resistance; obesity; polycystic ovarian syndrome; polycystic ovary syndrome; thinness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

restless legs syndrome; tourette syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease restless legs syndrome; tourette syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

endometriosis; infertility, female; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease endometriosis; infertility, female; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal alcohol syndrome; syndrome; fetal, alcohol (dysmorphic) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal alcohol syndrome; syndrome; fetal, alcohol (dysmorphic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

behcet syndrome; uveomeningoencephalitic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease behcet syndrome; uveomeningoencephalitic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperandrogenism; hyperinsulinism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperandrogenism; hyperinsulinism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune thyroiditis; helicobacter infections; thyroiditis, autoimmune; turner syndrome; xo syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune thyroiditis; helicobacter infections; thyroiditis, autoimmune; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infertility, female; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infertility, female; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melas syndrome; merrf syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease melas syndrome; merrf syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

haemolytic-uraemic syndrome; hemolytic-uremic syndrome; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease haemolytic-uraemic syndrome; hemolytic-uremic syndrome; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infertility; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease infertility; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; genetic diseases, inborn; kallmann syndrome; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; genetic diseases, inborn; kallmann syndrome; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

angelman syndrome; rett syndrome; seizures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angelman syndrome; rett syndrome; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis; carpal tunnel syndrome; cryoglobulinemia; hepatitis c, chronic; sjogren's syndrome; thyroiditis, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis; carpal tunnel syndrome; cryoglobulinemia; hepatitis c, chronic; sjogren's syndrome; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose intolerance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose intolerance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

escherichia coli infections; haemolytic-uraemic syndrome; hemolytic-uremic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease escherichia coli infections; haemolytic-uraemic syndrome; hemolytic-uremic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult respiratory distress syndrome; respiratory distress syndrome, adult Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

digeorge syndrome; memory disorders; pharyngeal pouch; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease digeorge syndrome; memory disorders; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult respiratory distress syndrome; chromosome deletion; respiratory distress syndrome, adult Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; chromosome deletion; respiratory distress syndrome, adult in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; noonan syndrome; pulmonary valve stenosis; syndrome; turner's phenotype, karyotype normal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; noonan syndrome; pulmonary valve stenosis; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; haemolytic-uraemic syndrome; hemolytic-uremic syndrome; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; haemolytic-uraemic syndrome; hemolytic-uremic syndrome; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

metabolic syndrome ; metabolic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease metabolic syndrome ; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

digeorge syndrome; pharyngeal pouch; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease digeorge syndrome; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fatigue; fatigue syndrome, chronic; fatigue syndrome; postviral Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fatigue; fatigue syndrome, chronic; fatigue syndrome; postviral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

haemolytic-uraemic syndrome; hemolytic-uremic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease haemolytic-uraemic syndrome; hemolytic-uremic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

inflammation; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease inflammation; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hantavirus infections; hantavirus pulmonary syndrome; heart diseases; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hantavirus infections; hantavirus pulmonary syndrome; heart diseases; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenomatous polyposis coli; bone neoplasms; epidermal cyst; gardner syndrome; gardner's syndrome; osteoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenomatous polyposis coli; bone neoplasms; epidermal cyst; gardner syndrome; gardner's syndrome; osteoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute lung injury; adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute lung injury; adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

down syndrome; ehlers-danlos syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease down syndrome; ehlers-danlos syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis; felty's syndrome; large granular lymphocyte syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis; felty's syndrome; large granular lymphocyte syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic ovarian syndrome; polycystic ovary syndrome; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease polycystic ovarian syndrome; polycystic ovary syndrome; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin resistance; metabolic syndrome x; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin resistance; metabolic syndrome x; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

menarch; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious Gene Set

From GAD Gene-Disease Associations

genes associated with the disease menarch; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart-hand syndrome, holt-oram syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart-hand syndrome, holt-oram syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gynecomastia; klinefelter syndrome; klinefelter's syndrome; oligospermia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gynecomastia; klinefelter syndrome; klinefelter's syndrome; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult respiratory distress syndrome; community-acquired infections; pneumonia; respiratory distress syndrome, adult; septic shock; shock, septic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; community-acquired infections; pneumonia; respiratory distress syndrome, adult; septic shock; shock, septic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aneurysm, dissecting; aortic aneurysm, thoracic; loeys-dietz syndrome; marfan syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aneurysm, dissecting; aortic aneurysm, thoracic; loeys-dietz syndrome; marfan syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; glucose intolerance; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; glucose intolerance; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hirsutism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hirsutism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

haemolytic-uraemic syndrome; hematologic diseases; hemolytic-uremic syndrome; purpura, thrombocytopenic; thrombocytopenic purpura Gene Set

From GAD Gene-Disease Associations

genes associated with the disease haemolytic-uraemic syndrome; hematologic diseases; hemolytic-uremic syndrome; purpura, thrombocytopenic; thrombocytopenic purpura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dwarfism, pituitary; pituitary dwarfism; turner syndrome; xo syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dwarfism, pituitary; pituitary dwarfism; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

stuve-wiedemann syndrome/schwartz-jampel type 2 syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the stuve-wiedemann syndrome/schwartz-jampel type 2 syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

digeorge syndrome/velocardiofacial syndrome complex-2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the digeorge syndrome/velocardiofacial syndrome complex-2 phenotype from the curated OMIM Gene-Disease Associations dataset.

ifap syndrome with or without bresheck syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ifap syndrome with or without bresheck syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Basic cell groups and regions Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Basic cell groups and regions relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

head and face region of M1 Gene Set

From Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles

genes with high or low expression in head and face region of M1 relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.

telomeres telomerase cellular aging and immortality Gene Set

From Biocarta Pathways

proteins participating in the telomeres telomerase cellular aging and immortality pathway from the Biocarta Pathways dataset.

mcalpain and friends in cell motility Gene Set

From Biocarta Pathways

proteins participating in the mcalpain and friends in cell motility pathway from the Biocarta Pathways dataset.

role of ppar-gamma coactivators in obesity and thermogenesis Gene Set

From Biocarta Pathways

proteins participating in the role of ppar-gamma coactivators in obesity and thermogenesis pathway from the Biocarta Pathways dataset.

il12 and stat4 dependent signaling pathway in th1 development Gene Set

From Biocarta Pathways

proteins participating in the il12 and stat4 dependent signaling pathway in th1 development pathway from the Biocarta Pathways dataset.

hypoxia and p53 in the cardiovascular system Gene Set

From Biocarta Pathways

proteins participating in the hypoxia and p53 in the cardiovascular system pathway from the Biocarta Pathways dataset.

lissencephaly gene (lis1) in neuronal migration and development Gene Set

From Biocarta Pathways

proteins participating in the lissencephaly gene (lis1) in neuronal migration and development pathway from the Biocarta Pathways dataset.

role of erbb2 in signal transduction and oncology Gene Set

From Biocarta Pathways

proteins participating in the role of erbb2 in signal transduction and oncology pathway from the Biocarta Pathways dataset.

corticosteroids and cardioprotection Gene Set

From Biocarta Pathways

proteins participating in the corticosteroids and cardioprotection pathway from the Biocarta Pathways dataset.

cyclins and cell cycle regulation Gene Set

From Biocarta Pathways

proteins participating in the cyclins and cell cycle regulation pathway from the Biocarta Pathways dataset.

mechanism of acetaminophen activity and toxicity Gene Set

From Biocarta Pathways

proteins participating in the mechanism of acetaminophen activity and toxicity pathway from the Biocarta Pathways dataset.

nfat and hypertrophy of the heart Gene Set

From Biocarta Pathways

proteins participating in the nfat and hypertrophy of the heart pathway from the Biocarta Pathways dataset.

acetylation and deacetylation of rela in nucleus Gene Set

From Biocarta Pathways

proteins participating in the acetylation and deacetylation of rela in nucleus pathway from the Biocarta Pathways dataset.

thrombin signaling and protease-activated receptors Gene Set

From Biocarta Pathways

proteins participating in the thrombin signaling and protease-activated receptors pathway from the Biocarta Pathways dataset.

antigen processing and presentation Gene Set

From Biocarta Pathways

proteins participating in the antigen processing and presentation pathway from the Biocarta Pathways dataset.

stathmin and breast cancer resistance to antimicrotubule agents Gene Set

From Biocarta Pathways

proteins participating in the stathmin and breast cancer resistance to antimicrotubule agents pathway from the Biocarta Pathways dataset.

role of ß-arrestins in the activation and targeting of map kinases Gene Set

From Biocarta Pathways

proteins participating in the role of ß-arrestins in the activation and targeting of map kinases pathway from the Biocarta Pathways dataset.

cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway Gene Set

From Biocarta Pathways

proteins participating in the cystic fibrosis transmembrane conductance regulator (cftr) and beta 2 adrenergic receptor (b2ar) pathway pathway from the Biocarta Pathways dataset.

role of pi3k subunit p85 in regulation of actin organization and cell migration Gene Set

From Biocarta Pathways

proteins participating in the role of pi3k subunit p85 in regulation of actin organization and cell migration pathway from the Biocarta Pathways dataset.

btg family proteins and cell cycle regulation Gene Set

From Biocarta Pathways

proteins participating in the btg family proteins and cell cycle regulation pathway from the Biocarta Pathways dataset.

control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) Gene Set

From Biocarta Pathways

proteins participating in the control of skeletal myogenesis by hdac and calcium/calmodulin-dependent kinase (camk) pathway from the Biocarta Pathways dataset.

endocytotic role of ndk phosphins and dynamin Gene Set

From Biocarta Pathways

proteins participating in the endocytotic role of ndk phosphins and dynamin pathway from the Biocarta Pathways dataset.

regulation of eif-4e and p70s6 kinase Gene Set

From Biocarta Pathways

proteins participating in the regulation of eif-4e and p70s6 kinase pathway from the Biocarta Pathways dataset.

estrogen responsive protein efp controls cell cycle and breast tumors growth Gene Set

From Biocarta Pathways

proteins participating in the estrogen responsive protein efp controls cell cycle and breast tumors growth pathway from the Biocarta Pathways dataset.

vegf hypoxia and angiogenesis Gene Set

From Biocarta Pathways

proteins participating in the vegf hypoxia and angiogenesis pathway from the Biocarta Pathways dataset.

yaci and bcma stimulation of b cell immune responses Gene Set

From Biocarta Pathways

proteins participating in the yaci and bcma stimulation of b cell immune responses pathway from the Biocarta Pathways dataset.

lck and fyn tyrosine kinases in initiation of tcr activation Gene Set

From Biocarta Pathways

proteins participating in the lck and fyn tyrosine kinases in initiation of tcr activation pathway from the Biocarta Pathways dataset.

hiv-1 nef: negative effector of fas and tnf Gene Set

From Biocarta Pathways

proteins participating in the hiv-1 nef: negative effector of fas and tnf pathway from the Biocarta Pathways dataset.

nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells Gene Set

From Biocarta Pathways

proteins participating in the nuclear receptors coordinate the activities of chromatin remodeling complexes and coactivators to facilitate initiation of transcription in carcinoma cells pathway from the Biocarta Pathways dataset.

ucalpain and friends in cell spread Gene Set

From Biocarta Pathways

proteins participating in the ucalpain and friends in cell spread pathway from the Biocarta Pathways dataset.

ionomycin and phorbal ester signaling pathway Gene Set

From Biocarta Pathways

proteins participating in the ionomycin and phorbal ester signaling pathway pathway from the Biocarta Pathways dataset.

carm1 and regulation of the estrogen receptor Gene Set

From Biocarta Pathways

proteins participating in the carm1 and regulation of the estrogen receptor pathway from the Biocarta Pathways dataset.

phosphoinositides and their downstream targets Gene Set

From Biocarta Pathways

proteins participating in the phosphoinositides and their downstream targets pathway from the Biocarta Pathways dataset.

melanocyte development and pigmentation pathway Gene Set

From Biocarta Pathways

proteins participating in the melanocyte development and pigmentation pathway pathway from the Biocarta Pathways dataset.

akap95 role in mitosis and chromosome dynamics Gene Set

From Biocarta Pathways

proteins participating in the akap95 role in mitosis and chromosome dynamics pathway from the Biocarta Pathways dataset.

transcription factor creb and its extracellular signals Gene Set

From Biocarta Pathways

proteins participating in the transcription factor creb and its extracellular signals pathway from the Biocarta Pathways dataset.

the igf-1 receptor and longevity Gene Set

From Biocarta Pathways

proteins participating in the the igf-1 receptor and longevity pathway from the Biocarta Pathways dataset.

cdc25 and chk1 regulatory pathway in response to dna damage Gene Set

From Biocarta Pathways

proteins participating in the cdc25 and chk1 regulatory pathway in response to dna damage pathway from the Biocarta Pathways dataset.

human cytomegalovirus and map kinase pathways Gene Set

From Biocarta Pathways

proteins participating in the human cytomegalovirus and map kinase pathways pathway from the Biocarta Pathways dataset.

influence of ras and rho proteins on g1 to s transition Gene Set

From Biocarta Pathways

proteins participating in the influence of ras and rho proteins on g1 to s transition pathway from the Biocarta Pathways dataset.

proteolysis and signaling pathway of notch Gene Set

From Biocarta Pathways

proteins participating in the proteolysis and signaling pathway of notch pathway from the Biocarta Pathways dataset.

apoptotic dna-fragmentation and tissue homeostasis Gene Set

From Biocarta Pathways

proteins participating in the apoptotic dna-fragmentation and tissue homeostasis pathway from the Biocarta Pathways dataset.

ion channels and their functional role in vascular endothelium Gene Set

From Biocarta Pathways

proteins participating in the ion channels and their functional role in vascular endothelium pathway from the Biocarta Pathways dataset.

alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease Gene Set

From Biocarta Pathways

proteins participating in the alpha-synuclein and parkin-mediated proteolysis in parkinson`s disease pathway from the Biocarta Pathways dataset.

fosb gene expression and drug abuse Gene Set

From Biocarta Pathways

proteins participating in the fosb gene expression and drug abuse pathway from the Biocarta Pathways dataset.

links between pyk2 and map kinases Gene Set

From Biocarta Pathways

proteins participating in the links between pyk2 and map kinases pathway from the Biocarta Pathways dataset.

opposing roles of aif in apoptosis and cell survival Gene Set

From Biocarta Pathways

proteins participating in the opposing roles of aif in apoptosis and cell survival pathway from