Name

Microcephaly, short stature, and impaired glucose metabolism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, short stature, and impaired glucose metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

microcephaly, short stature, and impaired glucose metabolism Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, short stature, and impaired glucose metabolism phenotype from the curated OMIM Gene-Disease Associations dataset.

short stature with microcephaly and distinctive facies Gene Set

From OMIM Gene-Disease Associations

genes associated with the short stature with microcephaly and distinctive facies phenotype from the curated OMIM Gene-Disease Associations dataset.

BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

childhood-onset short-trunk short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the childhood-onset short-trunk short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

neonatal short-trunk short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the neonatal short-trunk short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

disproportionate short-trunk short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the disproportionate short-trunk short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

disproportionate short-limb short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the disproportionate short-limb short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

lethal short-limbed short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the lethal short-limbed short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

childhood onset short-limb short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the childhood onset short-limb short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

neonatal short-limb short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the neonatal short-limb short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations 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.

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.

Short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, optic nerve atrophy, and pelger-huet anomaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Facial dysmorphism, immunodeficiency, livedo, and short stature Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Facial dysmorphism, immunodeficiency, livedo, and short stature phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked mental retardation with short stature, hypogonadism and abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease OSTEOCHONDRITIS DISSECANS, SHORT STATURE, AND EARLY-ONSET OSTEOARTHRITIS from the curated CTD Gene-Disease Associations dataset.

short stature, onychodysplasia, facial dysmorphism, and hypotrichosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the short stature, onychodysplasia, facial dysmorphism, and hypotrichosis 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.

osteochondritis dissecans, short stature, and early-onset osteoarthritis Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteochondritis dissecans, short stature, and early-onset osteoarthritis phenotype from the curated OMIM Gene-Disease Associations dataset.

short stature, optic nerve atrophy, and pelger-huet anomaly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short stature, optic nerve atrophy, and pelger-huet anomaly 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.

Short stature, idiopathic, autosomal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, idiopathic, autosomal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectodermal dysplasia/short stature syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectodermal dysplasia/short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, idiopathic, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, idiopathic, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Yakut short stature syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Yakut short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental Retardation, X-Linked, with Short Stature Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, X-Linked, with Short Stature from the curated CTD Gene-Disease Associations dataset.

Short Stature, Idiopathic, Autosomal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Short Stature, Idiopathic, Autosomal from the curated CTD Gene-Disease Associations dataset.

Short Stature, Idiopathic, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Short Stature, Idiopathic, X-Linked from the curated CTD Gene-Disease Associations dataset.

short stature Gene Set

From GAD Gene-Disease Associations

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

idiopathic short stature Gene Set

From GAD Gene-Disease Associations

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

moderately short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the moderately short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short stature Gene Set

From HPO Gene-Disease Associations

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

mesomelic short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the mesomelic short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

disproportionate short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the disproportionate short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

mild short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the mild short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

proportionate short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the proportionate short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

severe short stature Gene Set

From HPO Gene-Disease Associations

genes associated with the severe short stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

ectodermal dysplasia/short stature syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia/short stature syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

short stature Gene Set

From OMIM Gene-Disease Associations

genes associated with the short stature phenotype from the curated OMIM Gene-Disease Associations dataset.

short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities Gene Set

From OMIM Gene-Disease Associations

genes associated with the short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, x-linked, with short stature Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, x-linked, with short stature phenotype from the curated OMIM Gene-Disease Associations dataset.

short stature, idiopathic familial Gene Set

From OMIM Gene-Disease Associations

genes associated with the short stature, idiopathic familial phenotype from the curated OMIM Gene-Disease Associations dataset.

plasma glucose, basal hepatic glucose and increased insulin release Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma glucose, basal hepatic glucose and increased insulin release in GWAS and other genetic association datasets from the GAD 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.

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.

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.

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.

insulin in obese women with impaired glucose tolerance (igt) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin in obese women with impaired glucose tolerance (igt) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes or impaired glucose tolerance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes or impaired glucose tolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

impaired cellular glucose import Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired cellular glucose import phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired glucose tolerance Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired glucose tolerance phenotype in transgenic mice from the MPO Gene-Phenotype 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.

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.

spondyloepiphyseal dysplasia tall stature and precocious osteoarthritis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease spondyloepiphyseal dysplasia tall stature and precocious osteoarthritis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth height growth to adolescence and adult stature Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth height growth to adolescence and adult stature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Glucose Metabolism Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glucose Metabolism Disorders from the curated CTD Gene-Disease Associations dataset.

glucose metabolism disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

glucose metabolism disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease glucose metabolism disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

glucose metabolism disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

diabetes mellitus type ii; diabetes mellitus, type 2; glucose metabolism disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; glucose metabolism disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose metabolism Gene Set

From GAD Gene-Disease Associations

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

gastritis; glucose metabolism disorders; helicobacter infections; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gastritis; glucose metabolism disorders; helicobacter infections; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; lipid metabolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; lipid metabolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose metabolism disorders; obesity; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose metabolism disorders; obesity; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose metabolism disorders Gene Set

From GAD Gene-Disease Associations

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

glucose metabolism disease Gene Set

From GWASdb SNP-Disease Associations

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

Glucose Metabolism Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Glucose Metabolism Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Glucose metabolism Gene Set

From Reactome Pathways

proteins participating in the Glucose metabolism pathway from the Reactome Pathways 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.

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.

Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation 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.

Microcephaly and chorioretinopathy, autosomal recessive, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly and chorioretinopathy, autosomal recessive, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, normal intelligence and immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, normal intelligence and immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, postnatal progressive, with seizures and brain atrophy 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.

Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation from the curated CTD Gene-Disease Associations dataset.

MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROCEPHALY, POSTNATAL PROGRESSIVE, WITH SEIZURES AND BRAIN ATROPHY from the curated CTD Gene-Disease Associations dataset.

MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MICROCEPHALY, SEIZURES, AND DEVELOPMENTAL DELAY from the curated CTD Gene-Disease Associations dataset.

Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microcephaly, microphthalmia, ectrodactyly of lower limbs, and prognathism 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.

microcephaly, postnatal progressive, with seizures and brain atrophy Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, postnatal progressive, with seizures and brain atrophy phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, seizures, and developmental delay Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, seizures, and developmental delay 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.

severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene Set

From OMIM Gene-Disease Associations

genes associated with the severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly and chorioretinopathy, autosomal recessive, 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly and chorioretinopathy, autosomal recessive, 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly and chorioretinopathy, autosomal recessive, 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly and chorioretinopathy, autosomal recessive, 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

fluvoxamine metabolism; omeprazole metabolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fluvoxamine metabolism; omeprazole metabolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acrylonitrile metabolism/toxicity; ethylene oxide metabolism/toxicity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acrylonitrile metabolism/toxicity; ethylene oxide metabolism/toxicity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

omeprazole metabolism; sulfone metabolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease omeprazole metabolism; sulfone metabolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

reduced trans-activation impaired sperm production and male infertility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease reduced trans-activation impaired sperm production and male infertility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

impaired fasting glycemia and type 2 diabetes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease impaired fasting glycemia and type 2 diabetes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

impaired fsh and lh secretion Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired fsh and lh secretion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired pursuit initiation and maintenance Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired pursuit initiation and maintenance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

reduced serum c-peptide and insulin responses to an oral glucose challenge Gene Set

From GAD Gene-Disease Associations

genes associated with the disease reduced serum c-peptide and insulin responses to an oral glucose challenge in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma triglyceride and c-reactive protein, fasting glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma triglyceride and c-reactive protein, fasting glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity and glucose homeostasis Gene Set

From GAD Gene-Disease Associations

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

cortisol escape from dexamethasone and elevated glucose levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cortisol escape from dexamethasone and elevated glucose levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Synthesis, secretion, and inactivation of Glucose-dependent Insulinotropic Polypeptide (GIP) Gene Set

From Reactome Pathways

proteins participating in the Synthesis, secretion, and inactivation of Glucose-dependent Insulinotropic Polypeptide (GIP) pathway from the Reactome Pathways dataset.

heritability of stature Gene Set

From GAD Gene-Disease Associations

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

stature among african pygmies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease stature among african pygmies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

testosterone; bone density; stature Gene Set

From GAD Gene-Disease Associations

genes associated with the disease testosterone; bone density; stature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

stature Gene Set

From GeneRIF Biological Term Annotations

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

disproportionate tall stature Gene Set

From HPO Gene-Disease Associations

genes associated with the disproportionate tall stature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

tall stature Gene Set

From HPO Gene-Disease Associations

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

{stature qtl 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {stature qtl 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

{stature qtl 17} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {stature qtl 17} phenotype from the curated OMIM Gene-Disease Associations dataset.

{stature qtl 15} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {stature qtl 15} phenotype from the curated OMIM Gene-Disease Associations dataset.

{stature qtl 13} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {stature qtl 13} phenotype from the curated OMIM Gene-Disease Associations dataset.

{stature qtl 11} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {stature qtl 11} phenotype from the curated OMIM Gene-Disease Associations dataset.

{stature qtl 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {stature qtl 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

{stature qtl 23} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {stature qtl 23} phenotype from the curated OMIM Gene-Disease Associations dataset.

{stature qtl 21} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {stature qtl 21} phenotype from the curated OMIM Gene-Disease Associations dataset.

{stature qtl 5} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {stature qtl 5} phenotype from the curated OMIM Gene-Disease Associations dataset.

{stature qtl 7} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {stature qtl 7} phenotype from the curated OMIM Gene-Disease Associations dataset.

{stature qtl 16} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {stature qtl 16} phenotype from the curated OMIM Gene-Disease Associations dataset.

{stature qtl 14} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {stature qtl 14} phenotype from the curated OMIM Gene-Disease Associations dataset.

{stature qtl 12} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {stature qtl 12} phenotype from the curated OMIM Gene-Disease Associations dataset.

{stature qtl 19} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {stature qtl 19} phenotype from the curated OMIM Gene-Disease Associations dataset.

{stature qtl 10} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {stature qtl 10} phenotype from the curated OMIM Gene-Disease Associations dataset.

{stature qtl 18} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {stature qtl 18} phenotype from the curated OMIM Gene-Disease Associations dataset.

{stature qtl 8} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {stature qtl 8} phenotype from the curated OMIM Gene-Disease Associations dataset.

{stature qtl 22} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {stature qtl 22} phenotype from the curated OMIM Gene-Disease Associations dataset.

{stature qtl 20} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {stature qtl 20} phenotype from the curated OMIM Gene-Disease Associations dataset.

{stature qtl 4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {stature qtl 4} phenotype from the curated OMIM Gene-Disease Associations dataset.

{stature qtl 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {stature qtl 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

{stature qtl 24} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {stature qtl 24} phenotype from the curated OMIM Gene-Disease Associations dataset.

Primary autosomal recessive microcephaly 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary autosomal recessive microcephaly 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary autosomal recessive microcephaly 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary autosomal recessive microcephaly 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary autosomal recessive microcephaly 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary autosomal recessive microcephaly 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary autosomal recessive microcephaly 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary autosomal recessive microcephaly 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary autosomal recessive microcephaly 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary autosomal recessive microcephaly 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly 12, primary, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly 12, primary, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary autosomal recessive microcephaly 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary autosomal recessive microcephaly 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary autosomal recessive microcephaly 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary autosomal recessive microcephaly 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly 10, primary, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly 10, primary, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amish lethal microcephaly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amish lethal microcephaly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly-capillary malformation syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly-capillary malformation syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly 11, primary, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly 11, primary, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly with chorioretinopathy, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly with chorioretinopathy, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly 9, primary, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly 9, primary, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly 13, primary, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly 13, primary, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amish lethal microcephaly Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amish lethal microcephaly from the curated CTD Gene-Disease Associations dataset.

Microcephaly, Primary Autosomal Recessive, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microcephaly, Primary Autosomal Recessive, 5 from the curated CTD Gene-Disease Associations dataset.

Microcephaly, Primary Autosomal Recessive, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microcephaly, Primary Autosomal Recessive, 4 from the curated CTD Gene-Disease Associations dataset.

Microcephaly, Primary Autosomal Recessive, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microcephaly, Primary Autosomal Recessive, 6 from the curated CTD Gene-Disease Associations dataset.

Microcephaly, Primary Autosomal Recessive, 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microcephaly, Primary Autosomal Recessive, 7 from the curated CTD Gene-Disease Associations dataset.

Microcephaly, Primary Autosomal Recessive, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microcephaly, Primary Autosomal Recessive, 3 from the curated CTD Gene-Disease Associations dataset.

Microcephaly, Primary Autosomal Recessive, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microcephaly, Primary Autosomal Recessive, 1 from the curated CTD Gene-Disease Associations dataset.

Microcephaly Gene Set

From CTD Gene-Disease Associations

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

microcephaly Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

microcephaly Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

autosomal dominant microcephaly Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

microcephaly Gene Set

From GAD Gene-Disease Associations

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

micrencephaly ; microcephaly Gene Set

From GAD Gene-Disease Associations

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

mental retardation; microcephaly Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mental retardation; microcephaly in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

microcephaly Gene Set

From GeneRIF Biological Term Annotations

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

congenital microcephaly Gene Set

From HPO Gene-Disease Associations

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

progressive microcephaly Gene Set

From HPO Gene-Disease Associations

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

postnatal microcephaly Gene Set

From HPO Gene-Disease Associations

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

microcephaly Gene Set

From HPO Gene-Disease Associations

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

Microcephaly Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Abnormal spindle-like microcephaly-associated protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Abnormal spindle-like microcephaly-associated protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

microcephaly Gene Set

From MPO Gene-Phenotype Associations

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

microcephaly, amish type Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, amish type phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly-capillary malformation syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly-capillary malformation syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

?microcephaly 11, primary, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?microcephaly 11, primary, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly 2, primary, autosomal recessive, with or without cortical malformations Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly 2, primary, autosomal recessive, with or without cortical malformations phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly 5, primary, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly 5, primary, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly 9, primary, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly 9, primary, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly 6, primary, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly 6, primary, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly 1, primary, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly 1, primary, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

?microcephaly 8, primary, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?microcephaly 8, primary, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly 3, primary, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly 3, primary, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

periventricular heterotopia with microcephaly Gene Set

From OMIM Gene-Disease Associations

genes associated with the periventricular heterotopia with microcephaly phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly with or without chorioretinopathy, lymphedema, or mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly with or without chorioretinopathy, lymphedema, or mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly 4, primary, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly 4, primary, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

lissencephaly 4 (with microcephaly) Gene Set

From OMIM Gene-Disease Associations

genes associated with the lissencephaly 4 (with microcephaly) phenotype from the curated OMIM Gene-Disease Associations dataset.

?microcephaly 12, primary, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?microcephaly 12, primary, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly 7, primary, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly 7, primary, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

?microcephaly 13, primary, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?microcephaly 13, primary, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

?microcephaly 10, primary, autosomal recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?microcephaly 10, primary, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

genetically deficient metabolism of debrisoquine and other drugs Gene Set

From GAD Gene-Disease Associations

genes associated with the disease genetically deficient metabolism of debrisoquine and other drugs in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lead and mercury metabolism Gene Set

From GAD Gene-Disease Associations

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

homocysteine metabolism, cognition, and white matter lesions Gene Set

From GAD Gene-Disease Associations

genes associated with the disease homocysteine metabolism, cognition, and white matter lesions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipid metabolism and adiposity Gene Set

From GAD Gene-Disease Associations

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

thyroid hormone metabolism II (via conjugation and/or degradation) Gene Set

From HumanCyc Pathways

proteins participating in the thyroid hormone metabolism II (via conjugation and/or degradation) pathway from the HumanCyc Pathways dataset.

sphingosine and sphingosine-1-phosphate metabolism Gene Set

From HumanCyc Pathways

proteins participating in the sphingosine and sphingosine-1-phosphate metabolism pathway from the HumanCyc Pathways dataset.

thyronamine and iodothyronamine metabolism Gene Set

From HumanCyc Pathways

proteins participating in the thyronamine and iodothyronamine metabolism pathway from the HumanCyc Pathways dataset.

androgen and estrogen metabolism Gene Set

From KEGG Pathways

proteins participating in the androgen and estrogen metabolism pathway from the KEGG Pathways dataset.

d glutamine and d glutamate metabolism Gene Set

From KEGG Pathways

proteins participating in the d glutamine and d glutamate metabolism pathway from the KEGG Pathways dataset.

glyoxylate and dicarboxylate metabolism Gene Set

From KEGG Pathways

proteins participating in the glyoxylate and dicarboxylate metabolism pathway from the KEGG Pathways dataset.

glycine serine and threonine metabolism Gene Set

From KEGG Pathways

proteins participating in the glycine serine and threonine metabolism pathway from the KEGG Pathways dataset.

arginine and proline metabolism Gene Set

From KEGG Pathways

proteins participating in the arginine and proline metabolism pathway from the KEGG Pathways dataset.

urea cycle and metabolism of amino groups Gene Set

From KEGG Pathways

proteins participating in the urea cycle and metabolism of amino groups pathway from the KEGG Pathways dataset.

taurine and hypotaurine metabolism Gene Set

From KEGG Pathways

proteins participating in the taurine and hypotaurine metabolism pathway from the KEGG Pathways dataset.

starch and sucrose metabolism Gene Set

From KEGG Pathways

proteins participating in the starch and sucrose metabolism pathway from the KEGG Pathways dataset.

nicotinate and nicotinamide metabolism Gene Set

From KEGG Pathways

proteins participating in the nicotinate and nicotinamide metabolism pathway from the KEGG Pathways dataset.

fructose and mannose metabolism Gene Set

From KEGG Pathways

proteins participating in the fructose and mannose metabolism pathway from the KEGG Pathways dataset.

porphyrin and chlorophyll metabolism Gene Set

From KEGG Pathways

proteins participating in the porphyrin and chlorophyll metabolism pathway from the KEGG Pathways dataset.

ascorbate and aldarate metabolism Gene Set

From KEGG Pathways

proteins participating in the ascorbate and aldarate metabolism pathway from the KEGG Pathways dataset.

alanine and aspartate metabolism Gene Set

From KEGG Pathways

proteins participating in the alanine and aspartate metabolism pathway from the KEGG Pathways dataset.

d arginine and d ornithine metabolism Gene Set

From KEGG Pathways

proteins participating in the d arginine and d ornithine metabolism pathway from the KEGG Pathways dataset.

Vitamin D metabolism and pathway Gene Set

From PANTHER Pathways

proteins participating in the Vitamin D metabolism and pathway pathway from the PANTHER Pathways dataset.

Abacavir transport and metabolism Gene Set

From Reactome Pathways

proteins participating in the Abacavir transport and metabolism pathway from the Reactome Pathways dataset.

Neurotransmitter uptake and Metabolism In Glial Cells Gene Set

From Reactome Pathways

proteins participating in the Neurotransmitter uptake and Metabolism In Glial Cells pathway from the Reactome Pathways dataset.

Biotin transport and metabolism Gene Set

From Reactome Pathways

proteins participating in the Biotin transport and metabolism pathway from the Reactome Pathways dataset.

Retinoid metabolism and transport Gene Set

From Reactome Pathways

proteins participating in the Retinoid metabolism and transport pathway from the Reactome Pathways dataset.

Metabolism of folate and pterines Gene Set

From Reactome Pathways

proteins participating in the Metabolism of folate and pterines pathway from the Reactome Pathways dataset.

Metabolism of steroid hormones and vitamin D Gene Set

From Reactome Pathways

proteins participating in the Metabolism of steroid hormones and vitamin D pathway from the Reactome Pathways dataset.

alpha-linolenic (omega3) and linoleic (omega6) acid metabolism Gene Set

From Reactome Pathways

proteins participating in the alpha-linolenic (omega3) and linoleic (omega6) acid metabolism pathway from the Reactome Pathways dataset.

Pyruvate metabolism and Citric Acid (TCA) cycle Gene Set

From Reactome Pathways

proteins participating in the Pyruvate metabolism and Citric Acid (TCA) cycle pathway from the Reactome Pathways dataset.

Astrocytic Glutamate-Glutamine Uptake And Metabolism Gene Set

From Reactome Pathways

proteins participating in the Astrocytic Glutamate-Glutamine Uptake And Metabolism pathway from the Reactome Pathways dataset.

Defects in vitamin and cofactor metabolism Gene Set

From Reactome Pathways

proteins participating in the Defects in vitamin and cofactor metabolism pathway from the Reactome Pathways dataset.

Metabolism of water-soluble vitamins and cofactors Gene Set

From Reactome Pathways

proteins participating in the Metabolism of water-soluble vitamins and cofactors pathway from the Reactome Pathways dataset.

Metabolism of lipids and lipoproteins Gene Set

From Reactome Pathways

proteins participating in the Metabolism of lipids and lipoproteins pathway from the Reactome Pathways dataset.

Metabolism of vitamins and cofactors Gene Set

From Reactome Pathways

proteins participating in the Metabolism of vitamins and cofactors pathway from the Reactome Pathways dataset.

Cobalamin (Cbl, vitamin B12) transport and metabolism Gene Set

From Reactome Pathways

proteins participating in the Cobalamin (Cbl, vitamin B12) transport and metabolism pathway from the Reactome Pathways dataset.

Fatty acid, triacylglycerol, and ketone body metabolism Gene Set

From Reactome Pathways

proteins participating in the Fatty acid, triacylglycerol, and ketone body metabolism pathway from the Reactome Pathways dataset.

Metabolism of amino acids and derivatives Gene Set

From Reactome Pathways

proteins participating in the Metabolism of amino acids and derivatives pathway from the Reactome Pathways dataset.

Bile acid and bile salt metabolism Gene Set

From Reactome Pathways

proteins participating in the Bile acid and bile salt metabolism pathway from the Reactome Pathways dataset.

Vitamin A and Carotenoid Metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Vitamin A and Carotenoid Metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Trans-sulfuration and one carbon metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Trans-sulfuration and one carbon metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Glutathione and one carbon metabolism(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Glutathione and one carbon metabolism(Mus musculus) pathway from the Wikipathways Pathways dataset.

One carbon metabolism and related pathways(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the One carbon metabolism and related pathways(Mus musculus) pathway from the Wikipathways Pathways dataset.

Selenium Metabolism and Selenoproteins(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Selenium Metabolism and Selenoproteins(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Urea cycle and metabolism of amino groups(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Urea cycle and metabolism of amino groups(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Alanine and aspartate metabolism(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Alanine and aspartate metabolism(Mus musculus) pathway from the Wikipathways Pathways dataset.

Alanine and aspartate metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Alanine and aspartate metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Nuclear receptors in lipid metabolism and toxicity(Mus musculus) Gene Set

From Wikipathways Pathways

proteins participating in the Nuclear receptors in lipid metabolism and toxicity(Mus musculus) pathway from the Wikipathways Pathways dataset.

Codeine and Morphine Metabolism(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Codeine and Morphine Metabolism(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Nuclear Receptors in Lipid Metabolism and Toxicity(Homo sapiens) Gene Set

From Wikipathways Pathways

proteins participating in the Nuclear Receptors in Lipid Metabolism and Toxicity(Homo sapiens) pathway from the Wikipathways Pathways dataset.

Triglyceride storage disease with impaired long-chain fatty acid oxidation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Triglyceride storage disease with impaired long-chain fatty acid oxidation from the curated CTD Gene-Disease Associations dataset.

impaired renal function disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease impaired renal function disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

impaired renal function disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

impaired proinsulin conversion Gene Set

From GAD Gene-Disease Associations

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

impaired exercise stress response Gene Set

From GAD Gene-Disease Associations

genes associated with the disease impaired exercise stress response in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

impaired glucagon suppression Gene Set

From GAD Gene-Disease Associations

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

impaired left ventricular function Gene Set

From GAD Gene-Disease Associations

genes associated with the disease impaired left ventricular function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

impaired fibrinolysis Gene Set

From GAD Gene-Disease Associations

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

impaired Gene Set

From GeneRIF Biological Term Annotations

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

impaired platelet aggregation Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the impaired platelet aggregation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

impaired left ventricular function Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the impaired left ventricular function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

impaired collagen-induced platelet aggregation Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired collagen-induced platelet aggregation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired adp-induced platelet aggregation Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired adp-induced platelet aggregation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired temperature sensation Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired temperature sensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired memory b-cell generation Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired memory b-cell generation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired distal vibration sensation Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired distal vibration sensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired distal tactile sensation Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired distal tactile sensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired vibration sensation in the lower limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired vibration sensation in the lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired pain sensation Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired pain sensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired renal uric acid clearance Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired renal uric acid clearance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired vibration sensation at ankles Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired vibration sensation at ankles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired convergence Gene Set

From HPO Gene-Disease Associations

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

impaired vibratory sensation Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired vibratory sensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired gluconeogenesis Gene Set

From HPO Gene-Disease Associations

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

impaired horizontal smooth pursuit Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired horizontal smooth pursuit phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired tactile sensation Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired tactile sensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired ig class switch recombination Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired ig class switch recombination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired ocular adduction Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired ocular adduction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired renal concentrating ability Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired renal concentrating ability phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired ocular abduction Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired ocular abduction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired thrombin-induced platelet aggregation Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired thrombin-induced platelet aggregation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired social interactions Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired social interactions phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired lymphocyte transformation with phytohemagglutinin Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired lymphocyte transformation with phytohemagglutinin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired left ventricular function Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired left ventricular function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired myocardial contractility Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired myocardial contractility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired neutrophil bactericidal activity Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired neutrophil bactericidal activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired smooth pursuit Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired smooth pursuit phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

emg: impaired neuromuscular transmission Gene Set

From HPO Gene-Disease Associations

genes associated with the emg: impaired neuromuscular transmission phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired thermal sensitivity Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired thermal sensitivity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired use of nonverbal behaviors Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired use of nonverbal behaviors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired t cell function Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired t cell function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired proprioception Gene Set

From HPO Gene-Disease Associations

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

impaired epinephrine-induced platelet aggregation Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired epinephrine-induced platelet aggregation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired platelet aggregation Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired platelet aggregation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired reabsorption of chloride Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired reabsorption of chloride phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired distal proprioception Gene Set

From HPO Gene-Disease Associations

genes associated with the impaired distal proprioception phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

impaired neutrophil recruitment Gene Set

From MPO Gene-Phenotype Associations

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

impaired passive avoidance behavior Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired passive avoidance behavior phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired behavioral response to nicotine Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired behavioral response to nicotine phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired spatial learning Gene Set

From MPO Gene-Phenotype Associations

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

impaired macrophage chemotaxis Gene Set

From MPO Gene-Phenotype Associations

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

impaired behavioral response to xenobiotic Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired behavioral response to xenobiotic phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired basement membrane formation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired basement membrane formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired fibroblast cell migration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired fibroblast cell migration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired social transmission of food preference Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired social transmission of food preference phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired behavioral response to morphine Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired behavioral response to morphine phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired neural crest cell differentiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired neural crest cell differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired behavioral response to anesthetic Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired behavioral response to anesthetic phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired mammary gland growth during pregnancy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired mammary gland growth during pregnancy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired luteinization Gene Set

From MPO Gene-Phenotype Associations

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

impaired muscle contractility Gene Set

From MPO Gene-Phenotype Associations

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

impaired branching involved in terminal bronchiole morphogenesis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired branching involved in terminal bronchiole morphogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired cued conditioning behavior Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired cued conditioning behavior phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired myelopoiesis Gene Set

From MPO Gene-Phenotype Associations

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

impaired righting response Gene Set

From MPO Gene-Phenotype Associations

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

impaired granulocyte bactericidal activity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired granulocyte bactericidal activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired neuron differentiation Gene Set

From MPO Gene-Phenotype Associations

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

impaired neutrophil chemotaxis Gene Set

From MPO Gene-Phenotype Associations

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

impaired contractility of urinary bladder detrusor smooth muscle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired contractility of urinary bladder detrusor smooth muscle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired discrimination learning Gene Set

From MPO Gene-Phenotype Associations

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

impaired branching involved in preterminal bronchiole morphogenesis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired branching involved in preterminal bronchiole morphogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired eosinophil recruitment Gene Set

From MPO Gene-Phenotype Associations

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

impaired placental function Gene Set

From MPO Gene-Phenotype Associations

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

impaired exercise endurance Gene Set

From MPO Gene-Phenotype Associations

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

impaired eosinophil chemotaxis Gene Set

From MPO Gene-Phenotype Associations

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

impaired embryo implantation Gene Set

From MPO Gene-Phenotype Associations

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

impaired branching involved in ureteric bud morphogenesis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired branching involved in ureteric bud morphogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired lectin complement pathway Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired lectin complement pathway phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired ovarian folliculogenesis Gene Set

From MPO Gene-Phenotype Associations

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

impaired behavioral response to cocaine Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired behavioral response to cocaine phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired contractility of jejunal smooth muscle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired contractility of jejunal smooth muscle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired spacing of implantation sites Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired spacing of implantation sites phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired macrophage phagocytosis Gene Set

From MPO Gene-Phenotype Associations

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

impaired myofibroblast differentiation Gene Set

From MPO Gene-Phenotype Associations

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

impaired contextual conditioning behavior Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired contextual conditioning behavior phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired humoral immune response Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired humoral immune response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired pupillary reflex Gene Set

From MPO Gene-Phenotype Associations

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

impaired branching involved in bronchus morphogenesis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired branching involved in bronchus morphogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired learning Gene Set

From MPO Gene-Phenotype Associations

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

impaired gastric peristalsis Gene Set

From MPO Gene-Phenotype Associations

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

impaired luteal cell differentiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired luteal cell differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired coordination Gene Set

From MPO Gene-Phenotype Associations

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

impaired lipolysis Gene Set

From MPO Gene-Phenotype Associations

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

impaired contractility of ileal smooth muscle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired contractility of ileal smooth muscle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired ureteric peristalsis Gene Set

From MPO Gene-Phenotype Associations

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

impaired skin barrier function Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired skin barrier function phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired conditioning behavior Gene Set

From MPO Gene-Phenotype Associations

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

impaired mucociliary clearance Gene Set

From MPO Gene-Phenotype Associations

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

impaired skeletal muscle contractility Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired skeletal muscle contractility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired complement classical pathway Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired complement classical pathway phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired cardiac neural crest cell differentiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired cardiac neural crest cell differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired neutrophil phagocytosis Gene Set

From MPO Gene-Phenotype Associations

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

impaired fertilization Gene Set

From MPO Gene-Phenotype Associations

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

impaired skeletal muscle regeneration Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired skeletal muscle regeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired muscle relaxation Gene Set

From MPO Gene-Phenotype Associations

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

impaired balance Gene Set

From MPO Gene-Phenotype Associations

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

impaired hematopoiesis Gene Set

From MPO Gene-Phenotype Associations

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

impaired acrosome reaction Gene Set

From MPO Gene-Phenotype Associations

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

impaired swimming Gene Set

From MPO Gene-Phenotype Associations

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

impaired granulosa cell differentiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired granulosa cell differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired contractility of intestinal smooth muscle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired contractility of intestinal smooth muscle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired complement alternative pathway Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired complement alternative pathway phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired conditioned place preference behavior Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired conditioned place preference behavior phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired wound healing Gene Set

From MPO Gene-Phenotype Associations

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

impaired smooth muscle contractility Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired smooth muscle contractility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired olfaction Gene Set

From MPO Gene-Phenotype Associations

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

impaired hearing Gene Set

From MPO Gene-Phenotype Associations

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

impaired limb coordination Gene Set

From MPO Gene-Phenotype Associations

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

impaired branching involved in respiratory bronchiole morphogenesis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired branching involved in respiratory bronchiole morphogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired febrile response Gene Set

From MPO Gene-Phenotype Associations

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

impaired behavioral response to alcohol Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired behavioral response to alcohol phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired natural killer cell mediated cytotoxicity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired natural killer cell mediated cytotoxicity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired lung alveolus development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired lung alveolus development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired branching involved in trachea morphogenesis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired branching involved in trachea morphogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired ossification of basisphenoid bone Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired ossification of basisphenoid bone phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired muscle regeneration Gene Set

From MPO Gene-Phenotype Associations

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

impaired sperm capacitation Gene Set

From MPO Gene-Phenotype Associations

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

impaired branching involved in alveolar sac morphogenesis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired branching involved in alveolar sac morphogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired osteoblast differentiation Gene Set

From MPO Gene-Phenotype Associations

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

impaired somite development Gene Set

From MPO Gene-Phenotype Associations

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

impaired active avoidance behavior Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired active avoidance behavior phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired ability to fire action potentials Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired ability to fire action potentials phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired stratum corneum desquamation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired stratum corneum desquamation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired avoidance learning behavior Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired avoidance learning behavior phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired adaptive thermogenesis Gene Set

From MPO Gene-Phenotype Associations

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

impaired synaptic plasticity Gene Set

From MPO Gene-Phenotype Associations

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

impaired lung lobe morphogenesis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired lung lobe morphogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired behavioral response to addictive substance Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired behavioral response to addictive substance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

obesity with impaired prohormone processing Gene Set

From OMIM Gene-Disease Associations

genes associated with the obesity with impaired prohormone processing phenotype from the curated OMIM Gene-Disease Associations dataset.

clopidogrel, impaired responsiveness to Gene Set

From OMIM Gene-Disease Associations

genes associated with the clopidogrel, impaired responsiveness to phenotype from the curated OMIM Gene-Disease Associations dataset.

impaired Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term impaired in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

APC truncation mutants have impaired AXIN binding Gene Set

From Reactome Pathways

proteins participating in the APC truncation mutants have impaired AXIN binding pathway from the Reactome Pathways dataset.

short insular gyri, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

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

short insular gyri, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

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

Short rib-polydactyly syndrome, Majewski type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short rib-polydactyly syndrome, Majewski type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short-sleeper Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short-sleeper phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short-rib thoracic dysplasia 11 with or without polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

short QT syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the short QT syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital short bowel syndrome, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital short bowel syndrome, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short rib polydactyly syndrome 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short rib polydactyly syndrome 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short rib polydactyly syndrome 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short rib polydactyly syndrome 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short-rib thoracic dysplasia 10 with or without polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

SHORT syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Brachyrachia (short spine dysplasia) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Brachyrachia (short spine dysplasia) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Short-rib thoracic dysplasia 3 with or without polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondylometaepiphyseal dysplasia short limb-hand type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondylometaepiphyseal dysplasia short limb-hand type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

short-chain collagen trimer Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the short-chain collagen trimer cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

short-chain collagen trimer Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the short-chain collagen trimer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

Short QT Syndrome 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Short QT Syndrome 1 from the curated CTD Gene-Disease Associations dataset.

Short QT Syndrome 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Short QT Syndrome 3 from the curated CTD Gene-Disease Associations dataset.

Short QT Syndrome 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Short QT Syndrome 2 from the curated CTD Gene-Disease Associations dataset.

Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type from the curated CTD Gene-Disease Associations dataset.

Short Rib-Polydactyly Syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Short Rib-Polydactyly Syndrome from the curated CTD Gene-Disease Associations dataset.

Short chain Acyl CoA dehydrogenase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Short chain Acyl CoA dehydrogenase deficiency from the curated CTD Gene-Disease Associations dataset.

SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SHORT-RIB THORACIC DYSPLASIA 3 WITH OR WITHOUT POLYDACTYLY from the curated CTD Gene-Disease Associations dataset.

Memory, Short-Term Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Memory, Short-Term in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

short bowel syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

memory, short-term Gene Set

From GAD Gene-Disease Associations

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

multiple organ failure; short bowel syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease multiple organ failure; short bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

short-term response to haloperidol treatment Gene Set

From GAD Gene-Disease Associations

genes associated with the disease short-term response to haloperidol treatment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

short Gene Set

From GeneRIF Biological Term Annotations

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

16478745-SuppTable1-short Gene Set

From GeneSigDB Published Gene Signatures

genes in signature reported in the publication with PubMedID 16478745-SuppTable1-short from the GeneSigDB Published Gene Signatures dataset.

short-chain fatty acid metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the short-chain fatty acid metabolic process biological process from the curated GO Biological Process Annotations dataset.

regulation of short-term neuronal synaptic plasticity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of short-term neuronal synaptic plasticity biological process from the curated GO Biological Process Annotations dataset.

short-chain fatty acid transport Gene Set

From GO Biological Process Annotations

genes participating in the short-chain fatty acid transport biological process from the curated GO Biological Process Annotations dataset.

short-chain fatty acid biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the short-chain fatty acid biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

short-chain fatty acid import Gene Set

From GO Biological Process Annotations

genes participating in the short-chain fatty acid import biological process from the curated GO Biological Process Annotations dataset.

short-term memory Gene Set

From GO Biological Process Annotations

genes participating in the short-term memory biological process from the curated GO Biological Process Annotations dataset.

short-chain fatty acid catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the short-chain fatty acid catabolic process biological process from the curated GO Biological Process Annotations dataset.

short-chain collagen trimer Gene Set

From GO Cellular Component Annotations

proteins localized to the short-chain collagen trimer cellular component from the curated GO Cellular Component Annotations dataset.

short-chain fatty acid uptake transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the short-chain fatty acid uptake transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

short-chain carboxylesterase activity Gene Set

From GO Molecular Function Annotations

genes performing the short-chain carboxylesterase activity molecular function from the curated GO Molecular Function Annotations dataset.

short-chain fatty acid transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the short-chain fatty acid transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

Hypertension risk in short sleep duration Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Hypertension risk in short sleep duration phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

short attention span Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the short attention span phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

short distal phalanx of finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short distal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short nasal bridge Gene Set

From HPO Gene-Disease Associations

genes associated with the short nasal bridge phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short chordae tendineae of the tricuspid valve Gene Set

From HPO Gene-Disease Associations

genes associated with the short chordae tendineae of the tricuspid valve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short nose Gene Set

From HPO Gene-Disease Associations

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

short 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short 5th toe Gene Set

From HPO Gene-Disease Associations

genes associated with the short 5th toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short 4th toe Gene Set

From HPO Gene-Disease Associations

genes associated with the short 4th toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short diaphyses Gene Set

From HPO Gene-Disease Associations

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

short metacarpals with rounded proximal ends Gene Set

From HPO Gene-Disease Associations

genes associated with the short metacarpals with rounded proximal ends phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short 1st metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the short 1st metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short femoral neck Gene Set

From HPO Gene-Disease Associations

genes associated with the short femoral neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short digit Gene Set

From HPO Gene-Disease Associations

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

relatively short spine Gene Set

From HPO Gene-Disease Associations

genes associated with the relatively short spine phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short sacroiliac notch Gene Set

From HPO Gene-Disease Associations

genes associated with the short sacroiliac notch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short chordae tendineae of the mitral valve Gene Set

From HPO Gene-Disease Associations

genes associated with the short chordae tendineae of the mitral valve phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short columella Gene Set

From HPO Gene-Disease Associations

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

short nail Gene Set

From HPO Gene-Disease Associations

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

short fourth metatarsal Gene Set

From HPO Gene-Disease Associations

genes associated with the short fourth metatarsal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short humerus Gene Set

From HPO Gene-Disease Associations

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

short middle phalanx of finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short middle phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short philtrum Gene Set

From HPO Gene-Disease Associations

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

short metatarsal Gene Set

From HPO Gene-Disease Associations

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

short umbilical cord Gene Set

From HPO Gene-Disease Associations

genes associated with the short umbilical cord phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short upper lip Gene Set

From HPO Gene-Disease Associations

genes associated with the short upper lip phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short distal phalanx of the 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short distal phalanx of the 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short palpebral fissure Gene Set

From HPO Gene-Disease Associations

genes associated with the short palpebral fissure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short femur Gene Set

From HPO Gene-Disease Associations

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

short phalanx of the thumb Gene Set

From HPO Gene-Disease Associations

genes associated with the short phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short attention span Gene Set

From HPO Gene-Disease Associations

genes associated with the short attention span phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short 5th metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the short 5th metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short middle phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short middle phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short proximal phalanx of finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short proximal phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short chin Gene Set

From HPO Gene-Disease Associations

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

short thorax Gene Set

From HPO Gene-Disease Associations

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

short mandibular rami Gene Set

From HPO Gene-Disease Associations

genes associated with the short mandibular rami phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short lingual frenulum Gene Set

From HPO Gene-Disease Associations

genes associated with the short lingual frenulum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short 3rd metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the short 3rd metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short palm Gene Set

From HPO Gene-Disease Associations

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

short mandibular condyles Gene Set

From HPO Gene-Disease Associations

genes associated with the short mandibular condyles phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short 2nd toe Gene Set

From HPO Gene-Disease Associations

genes associated with the short 2nd toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short proximal phalanx of thumb Gene Set

From HPO Gene-Disease Associations

genes associated with the short proximal phalanx of thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short middle phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short middle phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short neck Gene Set

From HPO Gene-Disease Associations

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

severe short-limb dwarfism Gene Set

From HPO Gene-Disease Associations

genes associated with the severe short-limb dwarfism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short phalanx of finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short phalanx of finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short foot Gene Set

From HPO Gene-Disease Associations

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

short distal phalanx of the 5th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short distal phalanx of the 5th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short ribs Gene Set

From HPO Gene-Disease Associations

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

short proximal phalanx of hallux Gene Set

From HPO Gene-Disease Associations

genes associated with the short proximal phalanx of hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short 3rd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short 3rd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short ear Gene Set

From HPO Gene-Disease Associations

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

short toe Gene Set

From HPO Gene-Disease Associations

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

short thumb Gene Set

From HPO Gene-Disease Associations

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

short iliac bones Gene Set

From HPO Gene-Disease Associations

genes associated with the short iliac bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short lower limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the short lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short distal phalanx of the thumb Gene Set

From HPO Gene-Disease Associations

genes associated with the short distal phalanx of the thumb phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short phalanx of hallux Gene Set

From HPO Gene-Disease Associations

genes associated with the short phalanx of hallux phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short hard palate Gene Set

From HPO Gene-Disease Associations

genes associated with the short hard palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short nasal septum Gene Set

From HPO Gene-Disease Associations

genes associated with the short nasal septum phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short distal phalanx of toe Gene Set

From HPO Gene-Disease Associations

genes associated with the short distal phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short metacarpal Gene Set

From HPO Gene-Disease Associations

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

short distal phalanx of the 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short distal phalanx of the 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short long bone Gene Set

From HPO Gene-Disease Associations

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

short sternum Gene Set

From HPO Gene-Disease Associations

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

short 4th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short stepped shuffling gait Gene Set

From HPO Gene-Disease Associations

genes associated with the short stepped shuffling gait phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short distal phalanx of the 4th finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short distal phalanx of the 4th finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short tibia Gene Set

From HPO Gene-Disease Associations

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

short 2nd finger Gene Set

From HPO Gene-Disease Associations

genes associated with the short 2nd finger phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short 4th metacarpal Gene Set

From HPO Gene-Disease Associations

genes associated with the short 4th metacarpal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short tubular bones (hand) Gene Set

From HPO Gene-Disease Associations

genes associated with the short tubular bones (hand) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short clavicles Gene Set

From HPO Gene-Disease Associations

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

short middle phalanx of toe Gene Set

From HPO Gene-Disease Associations

genes associated with the short middle phalanx of toe phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short first metatarsal Gene Set

From HPO Gene-Disease Associations

genes associated with the short first metatarsal phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

short finger Gene Set

From HPO Gene-Disease Associations

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

short hallux Gene Set

From HPO Gene-Disease Associations

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

Short Bowel Syndrome Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Short Bowel Syndrome phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Memory, Short-Term Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Short hematopoietin receptor, family 1, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Short hematopoietin receptor, family 1, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Short hematopoietin receptor, family 2, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Short hematopoietin receptor, family 2, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Short-chain dehydrogenase/reductase, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Short-chain dehydrogenase/reductase, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Short-chain dehydrogenase/reductase SDR Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Short-chain dehydrogenase/reductase SDR protein domain from the InterPro Predicted Protein Domain Annotations dataset.

short nasal bone Gene Set

From MPO Gene-Phenotype Associations

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

short frontal bone Gene Set

From MPO Gene-Phenotype Associations

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

short perineum Gene Set

From MPO Gene-Phenotype Associations

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

short tail Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short tail 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.

short squamosal bone Gene Set

From MPO Gene-Phenotype Associations

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

short malleus manubrium Gene Set

From MPO Gene-Phenotype Associations

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

short metestrus Gene Set

From MPO Gene-Phenotype Associations

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

short metatarsal bones Gene Set

From MPO Gene-Phenotype Associations

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

short diestrus Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short diestrus 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.

short vertebral body Gene Set

From MPO Gene-Phenotype Associations

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

short zygomatic bone Gene Set

From MPO Gene-Phenotype Associations

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

short fibula Gene Set

From MPO Gene-Phenotype Associations

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

short palate Gene Set

From MPO Gene-Phenotype Associations

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

short premaxilla Gene Set

From MPO Gene-Phenotype Associations

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

short excitatory postsynaptic current decay time Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short excitatory postsynaptic current decay time phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short proestrus Gene Set

From MPO Gene-Phenotype Associations

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

short ureter Gene Set

From MPO Gene-Phenotype Associations

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

short humerus Gene Set

From MPO Gene-Phenotype Associations

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

short uterine horn Gene Set

From MPO Gene-Phenotype Associations

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

abnormal short term object recognition memory Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal short term object recognition memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short tibia Gene Set

From MPO Gene-Phenotype Associations

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

short radius Gene Set

From MPO Gene-Phenotype Associations

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

short ulna Gene Set

From MPO Gene-Phenotype Associations

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

short stride length Gene Set

From MPO Gene-Phenotype Associations

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

short vibrissae Gene Set

From MPO Gene-Phenotype Associations

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

short umbilical cord Gene Set

From MPO Gene-Phenotype Associations

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

short malleus Gene Set

From MPO Gene-Phenotype Associations

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

short hair Gene Set

From MPO Gene-Phenotype Associations

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

short lumbar vertebrae Gene Set

From MPO Gene-Phenotype Associations

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

short estrous cycle Gene Set

From MPO Gene-Phenotype Associations

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

short mandible Gene Set

From MPO Gene-Phenotype Associations

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

short rostral-caudal axis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short rostral-caudal axis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short cochlear hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short cochlear hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short maxilla Gene Set

From MPO Gene-Phenotype Associations

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

short kidney papilla Gene Set

From MPO Gene-Phenotype Associations

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

short outer hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short outer hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short endolymphatic duct Gene Set

From MPO Gene-Phenotype Associations

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

short oviduct Gene Set

From MPO Gene-Phenotype Associations

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

short presphenoid bone Gene Set

From MPO Gene-Phenotype Associations

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

short ribs Gene Set

From MPO Gene-Phenotype Associations

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

short snout Gene Set

From MPO Gene-Phenotype Associations

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

short vertebral column Gene Set

From MPO Gene-Phenotype Associations

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

short nails Gene Set

From MPO Gene-Phenotype Associations

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

short cochlear outer hair cells Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short cochlear outer hair cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short gestation period Gene Set

From MPO Gene-Phenotype Associations

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

short sternum Gene Set

From MPO Gene-Phenotype Associations

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

abnormal short term spatial reference memory Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal short term spatial reference memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short neck Gene Set

From MPO Gene-Phenotype Associations

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

short femur Gene Set

From MPO Gene-Phenotype Associations

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

short inner hair cell stereocilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the short inner hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

short sperm flagellum Gene Set

From MPO Gene-Phenotype Associations

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

short limbs Gene Set

From MPO Gene-Phenotype Associations

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

short metacarpal bones Gene Set

From MPO Gene-Phenotype Associations

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

short incisors Gene Set

From MPO Gene-Phenotype Associations

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

short scapula Gene Set

From MPO Gene-Phenotype Associations

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

short scala media Gene Set

From MPO Gene-Phenotype Associations

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

short trachea Gene Set

From MPO Gene-Phenotype Associations

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

short estrus Gene Set

From MPO Gene-Phenotype Associations

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

short syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the short syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 10 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 10 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 4 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 4 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

[short sleeper] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [short sleeper] phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 6 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 6 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 7 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 7 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

spondylometaepiphyseal dysplasia, short limb-hand type Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondylometaepiphyseal dysplasia, short limb-hand type phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 11 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 11 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital short bowel syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital short bowel syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

short qt syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the short qt syndrome 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

short qt syndrome 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the short qt syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

short qt syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the short qt syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 9 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 9 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

acyl-coa dehydrogenase, short-chain, deficiency of Gene Set

From OMIM Gene-Disease Associations

genes associated with the acyl-coa dehydrogenase, short-chain, deficiency of phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 3 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 3 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 8 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 8 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 2 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 2 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

short-rib thoracic dysplasia 5 with or without polydactyly Gene Set

From OMIM Gene-Disease Associations

genes associated with the short-rib thoracic dysplasia 5 with or without polydactyly phenotype from the curated OMIM Gene-Disease Associations dataset.

Congenital glucose-galactose malabsorption Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital glucose-galactose malabsorption phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glucose-6-phosphate transport defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glucose-6-phosphate transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glucose transporter type 1 deficiency syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glucose transporter type 1 deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

2-deoxy-D-glucose-344 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the 2-deoxy-D-glucose-344 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Glucose Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Glucose from the curated CTD Gene-Chemical Interactions dataset.

Glucose-6-Phosphate Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Glucose-6-Phosphate from the curated CTD Gene-Chemical Interactions dataset.

Uridine Diphosphate Glucose Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Uridine Diphosphate Glucose from the curated CTD Gene-Chemical Interactions dataset.

Blood Glucose Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Blood Glucose from the curated CTD Gene-Chemical Interactions dataset.

beta-penta-O-galloyl-glucose Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical beta-penta-O-galloyl-glucose from the curated CTD Gene-Chemical Interactions dataset.

glucose tolerance factor Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical glucose tolerance factor from the curated CTD Gene-Chemical Interactions dataset.

HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset.

Glucose Intolerance Gene Set

From CTD Gene-Disease Associations

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

Glucose-Galactose Malabsorption Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glucose-Galactose Malabsorption from the curated CTD Gene-Disease Associations dataset.

Blood Glucose Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Blood Glucose in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Glucose Tolerance Test Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Glucose Tolerance Test in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Glucose Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Glucose in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Glucose Transporter Type 2 Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Glucose Transporter Type 2 in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

glucose intolerance Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

4-Deoxy-Alpha-D-Glucose Gene Set

From DrugBank Drug Targets

interacting proteins for the 4-Deoxy-Alpha-D-Glucose drug from the curated DrugBank Drug Targets dataset.

4,6-Dideoxy-4-Amino-Alpha-D-Glucose Gene Set

From DrugBank Drug Targets

interacting proteins for the 4,6-Dideoxy-4-Amino-Alpha-D-Glucose drug from the curated DrugBank Drug Targets dataset.

Alpha-D-Glucose-6-Phosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the Alpha-D-Glucose-6-Phosphate drug from the curated DrugBank Drug Targets dataset.

2-Deoxy-2fluoro-Glucose Gene Set

From DrugBank Drug Targets

interacting proteins for the 2-Deoxy-2fluoro-Glucose drug from the curated DrugBank Drug Targets dataset.

Glucose-6-Phosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the Glucose-6-Phosphate drug from the curated DrugBank Drug Targets dataset.

Beta-D-Glucose Gene Set

From DrugBank Drug Targets

interacting proteins for the Beta-D-Glucose drug from the curated DrugBank Drug Targets dataset.

Alpha-D-Glucose 1,6-Bisphosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the Alpha-D-Glucose 1,6-Bisphosphate drug from the curated DrugBank Drug Targets dataset.

6-Deoxy-Alpha-D-Glucose Gene Set

From DrugBank Drug Targets

interacting proteins for the 6-Deoxy-Alpha-D-Glucose drug from the curated DrugBank Drug Targets dataset.

Alpha-D-Glucose-1-Phosphate-6-Vanadate Gene Set

From DrugBank Drug Targets

interacting proteins for the Alpha-D-Glucose-1-Phosphate-6-Vanadate drug from the curated DrugBank Drug Targets dataset.

Glucose-Uridine-C1,5'-Diphosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the Glucose-Uridine-C1,5'-Diphosphate drug from the curated DrugBank Drug Targets dataset.

Alpha-D-Glucose-1-Phosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the Alpha-D-Glucose-1-Phosphate drug from the curated DrugBank Drug Targets dataset.

2-Deoxy-Glucose-6-Phosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the 2-Deoxy-Glucose-6-Phosphate drug from the curated DrugBank Drug Targets dataset.

breast neoplasms; endometrial neoplasms; glucose intolerance; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; endometrial neoplasms; glucose intolerance; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; lipids; atherosclerosis, generalized Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; lipids; atherosclerosis, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass diabetes, type 2 glucose insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass diabetes, type 2 glucose insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose response Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; glucose intolerance; prediabetic state Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; glucose intolerance; prediabetic state in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; diabetes, type 2; insulin; glucose; hba(1c) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; diabetes, type 2; insulin; glucose; hba(1c) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma glucose levels Gene Set

From GAD Gene-Disease Associations

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

diabetes, type 2; insulin; glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; insulin; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose intolerance; obesity; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose intolerance; obesity; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; metabolic syndrome; hyperglycemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; metabolic syndrome; hyperglycemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose transporter type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose transporter type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; diabetes, type 2; leukemia; breast cancer; glucose; cytogenetic studies; birth weight; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; diabetes, type 2; leukemia; breast cancer; glucose; cytogenetic studies; birth weight; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; glucose intolerance; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; glucose intolerance; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol; cholesterol, hdl; triglycerides; cholesterol, ldl; hypertension; glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol; cholesterol, hdl; triglycerides; cholesterol, ldl; hypertension; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose; paraoxonase-1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose; paraoxonase-1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; insulin; glucose; c-peptide; fatty acid Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; insulin; glucose; c-peptide; fatty acid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; insulin; lipids; left ventricular hypertrophy; glucose; blood pressure, arterial; metabolic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; insulin; lipids; left ventricular hypertrophy; glucose; blood pressure, arterial; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; insulin; glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; insulin; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; insulin; vascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; insulin; vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; glucose Gene Set

From GAD Gene-Disease Associations

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

insulin; glucose Gene Set

From GAD Gene-Disease Associations

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

cerebral infarction; glucose intolerance; hyperhomocysteinemia; hyperlipidemias; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarction; glucose intolerance; hyperhomocysteinemia; hyperlipidemias; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; glucose intolerance; muscular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; glucose intolerance; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; glucose intolerance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; glucose intolerance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fasting plasma glucose Gene Set

From GAD Gene-Disease Associations

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

cholesterol; triglycerides; glucose tolerance; beta-cell function; insulin; lipids Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol; triglycerides; glucose tolerance; beta-cell function; insulin; lipids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance Gene Set

From GAD Gene-Disease Associations

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

insulin; lipids; obesity; glucose; leptin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin; lipids; obesity; glucose; leptin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; cholesterol; hypertension; glucose tolerance; insulin; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; cholesterol; hypertension; glucose tolerance; insulin; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose; birth weight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose; birth weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; triglycerides; cholesterol, ldl; cholesterol, total; glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; triglycerides; cholesterol, ldl; cholesterol, total; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; glucose; hba1c Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; glucose; hba1c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; insulin; lipids; obesity; glucose; blood pressure; cortisol, salivary; leptin; leptin; testosterone Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; insulin; lipids; obesity; glucose; blood pressure; cortisol, salivary; leptin; leptin; testosterone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

type 2 diabetes related glucose homeostasis trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease type 2 diabetes related glucose homeostasis trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; glucose tolerance; insulin; lipids; blood pressure, arterial; heart rate; autonomic nervous system Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; glucose tolerance; insulin; lipids; blood pressure, arterial; heart rate; autonomic nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; lipids; c-reactive protein; obesity; glucose; leptin; atopy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; lipids; c-reactive protein; obesity; glucose; leptin; atopy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; glucose tolerance; insulin; hematology indices Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; glucose tolerance; insulin; hematology indices in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

undetectable glucose-6-phosphate dehydrogenase enzyme activity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease undetectable glucose-6-phosphate dehydrogenase enzyme activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; cholesterol, ldl; glucose tolerance; blood pressure, arterial; glycosylated hemoglobin a1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; cholesterol, ldl; glucose tolerance; blood pressure, arterial; glycosylated hemoglobin a1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; insulin; body fat Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; insulin; body fat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

triglycerides; insulin; glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease triglycerides; insulin; glucose 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.

body mass; glucose tolerance; insulin; blood pressure; c-peptide; hba1c Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; glucose tolerance; insulin; blood pressure; c-peptide; hba1c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; insulin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; insulin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; triglycerides; cholesterol, ldl; cholesterol, total; glucose; stroke; carotid artery intima-media thickness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; triglycerides; cholesterol, ldl; cholesterol, total; glucose; stroke; carotid artery intima-media thickness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

type 2 diabetes related glucose homeostasis traits Gene Set

From GAD Gene-Disease Associations

genes associated with the disease type 2 diabetes related glucose homeostasis traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; insulin; glucose; nervous system activity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; insulin; glucose; nervous system activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol; triglycerides; hypertension; glucose tolerance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol; triglycerides; hypertension; glucose tolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; diabetes, type 2; insulin; glucose; body fat Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; diabetes, type 2; insulin; glucose; body fat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; lipids; glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; lipids; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin; lipids; glucose; cortisol; anthropometric parameters Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin; lipids; glucose; cortisol; anthropometric parameters in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin; lipids; obesity; glucose; leptin; cortisol Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin; lipids; obesity; glucose; leptin; cortisol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose; insulin secretion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose; insulin secretion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; glucose tolerance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; glucose tolerance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin sensitivity; glucose disposal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin sensitivity; glucose disposal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; lipids; fibrinogen; hematology indices Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; lipids; fibrinogen; hematology indices in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin; glucose; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

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

fasting glucose Gene Set

From GAD Gene-Disease Associations

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

reduced early insulin response to oral glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease reduced early insulin response to oral glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; glucose; insulin secretion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; glucose; insulin secretion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

elevated fasting blood glucose levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease elevated fasting blood glucose levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dyslipidemias; glucose intolerance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dyslipidemias; glucose intolerance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; overweight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose intolerance Gene Set

From GAD Gene-Disease Associations

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

glucose tolerance; fatty acid Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; fatty acid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose-stimulated beta cell function Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose-stimulated beta cell function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; glucose tolerance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; glucose tolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; glucose intolerance; obesity; overweight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; glucose intolerance; obesity; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; diabetes, type 2; glucose tolerance; insulin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; diabetes, type 2; glucose tolerance; insulin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin; lipids; glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin; lipids; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; cholesterol; triglycerides; insulin; glucose; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; cholesterol; triglycerides; insulin; glucose; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipids; obesity; glucose; cortisol Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lipids; obesity; glucose; cortisol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial diabetes, type 2 glucose insulin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial diabetes, type 2 glucose insulin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; metabolic syndrome; adiponectin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; metabolic syndrome; adiponectin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; insulin; polycystic ovary syndrome; androgen levels; anthropometric measuments Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; insulin; polycystic ovary syndrome; androgen levels; anthropometric measuments in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance test Gene Set

From GAD Gene-Disease Associations

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

insulin response to oral glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin response to oral glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; insulin; obesity; energy expenditure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; insulin; obesity; energy expenditure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipids; c-reactive protein; obesity; glucose; leptin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lipids; c-reactive protein; obesity; glucose; leptin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; insulin; polycystic ovary syndrome; hormone disturbance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; insulin; polycystic ovary syndrome; hormone disturbance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose Gene Set

From GAD Gene-Disease Associations

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

glucose; lactose intolerance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose; lactose intolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; glucose intolerance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; glucose intolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; glucose tolerance; metabolic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; glucose tolerance; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; adiponectin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; adiponectin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin; glucose; c-peptide; fatty acid Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin; glucose; c-peptide; fatty acid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

two-hour glucose challenge Gene Set

From GAD Gene-Disease Associations

genes associated with the disease two-hour glucose challenge in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; diabetes, type 2; glucose; birth weight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; diabetes, type 2; glucose; birth weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipids; glucose; c-peptide Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lipids; glucose; c-peptide in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

oral glucose tolerance Gene Set

From GAD Gene-Disease Associations

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

fasting glucose-related traits Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fasting glucose-related traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipids; glucose; atherosclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lipids; glucose; atherosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose; adiponectin Gene Set

From GAD Gene-Disease Associations

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

cholesterol; diabetes, type 2; insulin; glucose; insulin resistance; pc-1 protein content; systolic blood pressure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol; diabetes, type 2; insulin; glucose; insulin resistance; pc-1 protein content; systolic blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood glucose Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus; diabetic angiopathies; diabetic neuropathies; diabetic retinopathy; glucose intolerance; hemochromatosis; liver cirrhosis; proteinuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; diabetic angiopathies; diabetic neuropathies; diabetic retinopathy; glucose intolerance; hemochromatosis; liver cirrhosis; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

increased serum glucose concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease increased serum glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; metabolic syndrome x 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.

plasma glucose concentration Gene Set

From GAD Gene-Disease Associations

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

body mass; insulin; obesity; glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; insulin; obesity; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; glucose tolerance; insulin; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; glucose tolerance; insulin; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose homeostasis Gene Set

From GAD Gene-Disease Associations

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

glucose tolerance; insulin; blood pressure; body weight; c-peptide; hba1c Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; insulin; blood pressure; body weight; c-peptide; hba1c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose Gene Set

From GeneRIF Biological Term Annotations

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

negative regulation of transcription by glucose Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of transcription by glucose biological process from the curated GO Biological Process Annotations dataset.

glucose-6-phosphate transport Gene Set

From GO Biological Process Annotations

genes participating in the glucose-6-phosphate transport biological process from the curated GO Biological Process Annotations dataset.

negative regulation of udp-glucose catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of udp-glucose catabolic process biological process from the curated GO Biological Process Annotations dataset.

response to glucose Gene Set

From GO Biological Process Annotations

genes participating in the response to glucose biological process from the curated GO Biological Process Annotations dataset.

negative regulation of transcription from rna polymerase ii promoter by glucose Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of transcription from rna polymerase ii promoter by glucose biological process from the curated GO Biological Process Annotations dataset.

udp-glucose catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the udp-glucose catabolic process biological process from the curated GO Biological Process Annotations dataset.

glucose 6-phosphate metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the glucose 6-phosphate metabolic process biological process from the curated GO Biological Process Annotations dataset.

regulation of insulin secretion involved in cellular response to glucose stimulus Gene Set

From GO Biological Process Annotations

genes participating in the regulation of insulin secretion involved in cellular response to glucose stimulus biological process from the curated GO Biological Process Annotations dataset.

insulin secretion involved in cellular response to glucose stimulus Gene Set

From GO Biological Process Annotations

genes participating in the insulin secretion involved in cellular response to glucose stimulus biological process from the curated GO Biological Process Annotations dataset.

positive regulation of transcription by glucose Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of transcription by glucose biological process from the curated GO Biological Process Annotations dataset.

glucose metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the glucose metabolic process biological process from the curated GO Biological Process Annotations dataset.

positive regulation of glucose import Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of glucose import biological process from the curated GO Biological Process Annotations dataset.

regulation of detection of glucose Gene Set

From GO Biological Process Annotations

genes participating in the regulation of detection of glucose biological process from the curated GO Biological Process Annotations dataset.

positive regulation of glucose transport Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of glucose transport biological process from the curated GO Biological Process Annotations dataset.

glucose catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the glucose catabolic process biological process from the curated GO Biological Process Annotations dataset.

cellular response to glucose stimulus Gene Set

From GO Biological Process Annotations

genes participating in the cellular response to glucose stimulus biological process from the curated GO Biological Process Annotations dataset.

negative regulation of glucose transport Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of glucose transport biological process from the curated GO Biological Process Annotations dataset.

negative regulation of insulin secretion involved in cellular response to glucose stimulus Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of insulin secretion involved in cellular response to glucose stimulus biological process from the curated GO Biological Process Annotations dataset.

positive regulation of transcription from rna polymerase ii promoter by glucose Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of transcription from rna polymerase ii promoter by glucose biological process from the curated GO Biological Process Annotations dataset.

positive regulation of glucose import in response to insulin stimulus Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of glucose import in response to insulin stimulus biological process from the curated GO Biological Process Annotations dataset.

negative regulation of glucose import Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of glucose import biological process from the curated GO Biological Process Annotations dataset.

negative regulation of glucose import in response to insulin stimulus Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of glucose import in response to insulin stimulus biological process from the curated GO Biological Process Annotations dataset.

glucose mediated signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the glucose mediated signaling pathway biological process from the curated GO Biological Process Annotations dataset.

glucose import Gene Set

From GO Biological Process Annotations

genes participating in the glucose import biological process from the curated GO Biological Process Annotations dataset.

regulation of glucose transport Gene Set

From GO Biological Process Annotations

genes participating in the regulation of glucose transport biological process from the curated GO Biological Process Annotations dataset.

glucose transport Gene Set

From GO Biological Process Annotations

genes participating in the glucose transport biological process from the curated GO Biological Process Annotations dataset.

cellular response to glucose starvation Gene Set

From GO Biological Process Annotations

genes participating in the cellular response to glucose starvation biological process from the curated GO Biological Process Annotations dataset.

glucose 1-phosphate metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the glucose 1-phosphate metabolic process biological process from the curated GO Biological Process Annotations dataset.

cellular glucose homeostasis Gene Set

From GO Biological Process Annotations

genes participating in the cellular glucose homeostasis biological process from the curated GO Biological Process Annotations dataset.

regulation of transcription by glucose Gene Set

From GO Biological Process Annotations

genes participating in the regulation of transcription by glucose biological process from the curated GO Biological Process Annotations dataset.

regulation of udp-glucose catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the regulation of udp-glucose catabolic process biological process from the curated GO Biological Process Annotations dataset.

regulation of glucose import in response to insulin stimulus Gene Set

From GO Biological Process Annotations

genes participating in the regulation of glucose import in response to insulin stimulus biological process from the curated GO Biological Process Annotations dataset.

udp-glucose metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the udp-glucose metabolic process biological process from the curated GO Biological Process Annotations dataset.

positive regulation of insulin secretion involved in cellular response to glucose stimulus Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of insulin secretion involved in cellular response to glucose stimulus biological process from the curated GO Biological Process Annotations dataset.

detection of glucose Gene Set

From GO Biological Process Annotations

genes participating in the detection of glucose biological process from the curated GO Biological Process Annotations dataset.

renal glucose absorption Gene Set

From GO Biological Process Annotations

genes participating in the renal glucose absorption biological process from the curated GO Biological Process Annotations dataset.

regulation of glucose import Gene Set

From GO Biological Process Annotations

genes participating in the regulation of glucose import biological process from the curated GO Biological Process Annotations dataset.

regulation of transcription from rna polymerase ii promoter by glucose Gene Set

From GO Biological Process Annotations

genes participating in the regulation of transcription from rna polymerase ii promoter by glucose biological process from the curated GO Biological Process Annotations dataset.

negative regulation of detection of glucose Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of detection of glucose biological process from the curated GO Biological Process Annotations dataset.

regulation of gluconeogenesis involved in cellular glucose homeostasis Gene Set

From GO Biological Process Annotations

genes participating in the regulation of gluconeogenesis involved in cellular glucose homeostasis biological process from the curated GO Biological Process Annotations dataset.

regulation of glucose metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the regulation of glucose metabolic process biological process from the curated GO Biological Process Annotations dataset.

glucose homeostasis Gene Set

From GO Biological Process Annotations

genes participating in the glucose homeostasis biological process from the curated GO Biological Process Annotations dataset.

positive regulation of glucose metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of glucose metabolic process biological process from the curated GO Biological Process Annotations dataset.

udp-glucose 6-dehydrogenase activity Gene Set

From GO Molecular Function Annotations

genes performing the udp-glucose 6-dehydrogenase activity molecular function from the curated GO Molecular Function Annotations dataset.

glycogen synthase activity, transferring glucose-1-phosphate Gene Set

From GO Molecular Function Annotations

genes performing the glycogen synthase activity, transferring glucose-1-phosphate molecular function from the curated GO Molecular Function Annotations dataset.

glucose binding Gene Set

From GO Molecular Function Annotations

genes performing the glucose binding molecular function from the curated GO Molecular Function Annotations dataset.

glucose transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the glucose transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

glucose 1-dehydrogenase [nad(p)] activity Gene Set

From GO Molecular Function Annotations

genes performing the glucose 1-dehydrogenase [nad(p)] activity molecular function from the curated GO Molecular Function Annotations dataset.

glucose-6-phosphate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the glucose-6-phosphate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

d-glucose transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the d-glucose transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

glucose:sodium symporter activity Gene Set

From GO Molecular Function Annotations

genes performing the glucose:sodium symporter activity molecular function from the curated GO Molecular Function Annotations dataset.

glucose-6-phosphate dehydrogenase activity Gene Set

From GO Molecular Function Annotations

genes performing the glucose-6-phosphate dehydrogenase activity molecular function from the curated GO Molecular Function Annotations dataset.

udp-glucose:glycoprotein glucosyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the udp-glucose:glycoprotein glucosyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

udp-glucose:hexose-1-phosphate uridylyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the udp-glucose:hexose-1-phosphate uridylyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

udp-glucose 4-epimerase activity Gene Set

From GO Molecular Function Annotations

genes performing the udp-glucose 4-epimerase activity molecular function from the curated GO Molecular Function Annotations dataset.

gdp-d-glucose phosphorylase activity Gene Set

From GO Molecular Function Annotations

genes performing the gdp-d-glucose phosphorylase activity molecular function from the curated GO Molecular Function Annotations dataset.

utp:glucose-1-phosphate uridylyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the utp:glucose-1-phosphate uridylyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

glucose-1,6-bisphosphate synthase activity Gene Set

From GO Molecular Function Annotations

genes performing the glucose-1,6-bisphosphate synthase activity molecular function from the curated GO Molecular Function Annotations dataset.

low-affinity glucose:sodium symporter activity Gene Set

From GO Molecular Function Annotations

genes performing the low-affinity glucose:sodium symporter activity molecular function from the curated GO Molecular Function Annotations dataset.

dtdp-glucose 4,6-dehydratase activity Gene Set

From GO Molecular Function Annotations

genes performing the dtdp-glucose 4,6-dehydratase activity molecular function from the curated GO Molecular Function Annotations dataset.

glucose-6-phosphate isomerase activity Gene Set

From GO Molecular Function Annotations

genes performing the glucose-6-phosphate isomerase activity molecular function from the curated GO Molecular Function Annotations dataset.

glucose-6-phosphatase activity Gene Set

From GO Molecular Function Annotations

genes performing the glucose-6-phosphatase activity molecular function from the curated GO Molecular Function Annotations dataset.

UDP-glucose Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the UDP-glucose ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

Fasting plasma glucose Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Fasting plasma glucose phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Fasting glucose-related traits Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Fasting glucose-related traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Two-hour glucose challenge Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Two-hour glucose challenge phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Fasting glucose-related traits (interaction with BMI) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Fasting glucose-related traits (interaction with BMI) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

abnormal glucose homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal glucose homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

dTDP-D-glucose Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the dTDP-D-glucose metabolite from the curated HMDB Metabolites of Enzymes dataset.

Glucose 1-phosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Glucose 1-phosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

Beta-D-Glucose Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Beta-D-Glucose metabolite from the curated HMDB Metabolites of Enzymes dataset.

Glucose 6-phosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Glucose 6-phosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

D-Gal alpha 1->6D-Gal alpha 1->6D-Glucose Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the D-Gal alpha 1->6D-Gal alpha 1->6D-Glucose metabolite from the curated HMDB Metabolites of Enzymes dataset.

Uridine diphosphate glucose Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Uridine diphosphate glucose metabolite from the curated HMDB Metabolites of Enzymes dataset.

4,6-Dideoxy-4-oxo-dTDP-D-glucose Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 4,6-Dideoxy-4-oxo-dTDP-D-glucose metabolite from the curated HMDB Metabolites of Enzymes dataset.

Beta-D-Glucose 6-phosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Beta-D-Glucose 6-phosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

Alpha-D-Glucose 1,6-bisphosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Alpha-D-Glucose 1,6-bisphosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

D-Glucose Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the D-Glucose metabolite from the curated HMDB Metabolites of Enzymes dataset.

Alpha-D-Glucose Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Alpha-D-Glucose metabolite from the curated HMDB Metabolites of Enzymes dataset.

GDP-glucose Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the GDP-glucose metabolite from the curated HMDB Metabolites of Enzymes dataset.

abnormality of blood glucose concentration Gene Set

From HPO Gene-Disease Associations

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

abnormal glucose homeostasis Gene Set

From HPO Gene-Disease Associations

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

glucose intolerance Gene Set

From HPO Gene-Disease Associations

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

abnormality of urine glucose concentration Gene Set

From HPO Gene-Disease Associations

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

abnormal oral glucose tolerance Gene Set

From HPO Gene-Disease Associations

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

abnormal glucose tolerance Gene Set

From HPO Gene-Disease Associations

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

Glucose Intolerance Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

GDP-glucose biosynthesis II Gene Set

From HumanCyc Pathways

proteins participating in the GDP-glucose biosynthesis II pathway from the HumanCyc Pathways dataset.

Glucose-6-phosphate dehydrogenase, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-6-phosphate dehydrogenase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-dependent insulinotropic receptor Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-dependent insulinotropic receptor protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-inhibited division protein A-related, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-inhibited division protein A-related, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

UDP-glucose 4-epimerase GalE Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UDP-glucose 4-epimerase GalE protein domain from the InterPro Predicted Protein Domain Annotations dataset.

UDP-glucose/GDP-mannose dehydrogenase, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UDP-glucose/GDP-mannose dehydrogenase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose transporter, type 2 (GLUT2) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose transporter, type 2 (GLUT2) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-6-phosphate dehydrogenase, NAD-binding Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-6-phosphate dehydrogenase, NAD-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose transporter, type 3 (GLUT3) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose transporter, type 3 (GLUT3) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

UDP-glucose:Glycoprotein Glucosyltransferase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UDP-glucose:Glycoprotein Glucosyltransferase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

UDP-glucose/GDP-mannose dehydrogenase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UDP-glucose/GDP-mannose dehydrogenase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose/Sorbosone dehydrogenase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose/Sorbosone dehydrogenase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

UDP-glucose/GDP-mannose dehydrogenase, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UDP-glucose/GDP-mannose dehydrogenase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-6-phosphate dehydrogenase, active site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-6-phosphate dehydrogenase, active site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

dTDP-glucose 4,6-dehydratase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the dTDP-glucose 4,6-dehydratase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

UDP-glucose/GDP-mannose dehydrogenase, dimerisation Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UDP-glucose/GDP-mannose dehydrogenase, dimerisation protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aldose 1-/Glucose-6-phosphate 1-epimerase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aldose 1-/Glucose-6-phosphate 1-epimerase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-methanol-choline oxidoreductase, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-methanol-choline oxidoreductase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

GDP-L-galactose/GDP-D-glucose phosphorylase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the GDP-L-galactose/GDP-D-glucose phosphorylase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

UDP-glucose 4-epimerase C-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UDP-glucose 4-epimerase C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

UTP--glucose-1-phosphate uridylyltransferase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UTP--glucose-1-phosphate uridylyltransferase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose/ribitol dehydrogenase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose/ribitol dehydrogenase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose transporter, type 1 (GLUT1) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose transporter, type 1 (GLUT1) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

UTP--glucose-1-phosphate uridylyltransferase family Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UTP--glucose-1-phosphate uridylyltransferase family protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-6-phosphate dehydrogenase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-6-phosphate dehydrogenase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-methanol-choline oxidoreductase, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-methanol-choline oxidoreductase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Soluble quinoprotein glucose/sorbosone dehydrogenase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Soluble quinoprotein glucose/sorbosone dehydrogenase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose transporter, type 4 (GLUT4) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose transporter, type 4 (GLUT4) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-methanol-choline oxidoreductase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-methanol-choline oxidoreductase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

UDP-glucose 6-dehydrogenase, eukaryotic type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UDP-glucose 6-dehydrogenase, eukaryotic type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-inhibited division protein A-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-inhibited division protein A-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-6-phosphatase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-6-phosphatase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal muscle cell glucose uptake Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal muscle cell glucose uptake phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased urine glucose level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased urine glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased urine glucose level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased urine glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal renal glucose reabsorption Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal renal glucose reabsorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal glucose homeostasis Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cellular glucose import Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cellular glucose import phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal glucose absorption Gene Set

From MPO Gene-Phenotype Associations

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

abnormal glucose tolerance Gene Set

From MPO Gene-Phenotype Associations

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

decreased circulating glucose level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased circulating glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

enhanced cellular glucose import Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the enhanced cellular glucose import phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal circulating glucose level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal circulating glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal urine glucose level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal urine glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal adipocyte glucose uptake Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal adipocyte glucose uptake phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cardiac cell glucose uptake Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cardiac cell glucose uptake phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

improved glucose tolerance Gene Set

From MPO Gene-Phenotype Associations

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

decreased fasted circulating glucose level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased fasted circulating glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal fasted circulating glucose level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal fasted circulating glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased fasted circulating glucose level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased fasted circulating glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased circulating glucose level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased circulating glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

[fasting plasma glucose level qtl 5] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [fasting plasma glucose level qtl 5] phenotype from the curated OMIM Gene-Disease Associations dataset.

[fasting plasma glucose level qtl 4] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [fasting plasma glucose level qtl 4] phenotype from the curated OMIM Gene-Disease Associations dataset.

hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

[fasting plasma glucose level qtl 6] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [fasting plasma glucose level qtl 6] phenotype from the curated OMIM Gene-Disease Associations dataset.

glucose/galactose malabsorption Gene Set

From OMIM Gene-Disease Associations

genes associated with the glucose/galactose malabsorption phenotype from the curated OMIM Gene-Disease Associations dataset.

[fasting plasma glucose level qtl 2] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [fasting plasma glucose level qtl 2] phenotype from the curated OMIM Gene-Disease Associations dataset.

[plasma glucose, 2-hour, qtl 2] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [plasma glucose, 2-hour, qtl 2] phenotype from the curated OMIM Gene-Disease Associations dataset.

[plasma glucose, 2-hour, qtl 1] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [plasma glucose, 2-hour, qtl 1] phenotype from the curated OMIM Gene-Disease Associations dataset.

[fasting plasma glucose level qtl 1] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [fasting plasma glucose level qtl 1] phenotype from the curated OMIM Gene-Disease Associations dataset.

[fasting plasma glucose level qtl 3] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [fasting plasma glucose level qtl 3] phenotype from the curated OMIM Gene-Disease Associations dataset.

p53 pathway by glucose deprivation Gene Set

From PANTHER Pathways

proteins participating in the p53 pathway by glucose deprivation pathway from the PANTHER Pathways dataset.

glucose Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term glucose in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

Insulin-mediated glucose transport Gene Set

From PID Pathways

proteins participating in the Insulin-mediated glucose transport pathway from the PID Pathways dataset.

Synthesis of dolichyl-phosphate-glucose Gene Set

From Reactome Pathways

proteins participating in the Synthesis of dolichyl-phosphate-glucose pathway from the Reactome Pathways dataset.

Na+-dependent glucose transporters Gene Set

From Reactome Pathways

proteins participating in the Na+-dependent glucose transporters pathway from the Reactome Pathways dataset.

Glucose transport Gene Set

From Reactome Pathways

proteins participating in the Glucose transport pathway from the Reactome Pathways dataset.

Facilitative Na+-independent glucose transporters Gene Set

From Reactome Pathways

proteins participating in the Facilitative Na+-independent glucose transporters pathway from the Reactome Pathways 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.

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.

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.

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.

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.

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.

metabolism of anandamide an endogenous cannabinoid Gene Set

From Biocarta Pathways

proteins participating in the metabolism of anandamide an endogenous cannabinoid pathway from the Biocarta Pathways dataset.

eicosanoid metabolism Gene Set

From Biocarta Pathways

proteins participating in the eicosanoid metabolism pathway from the Biocarta Pathways dataset.

Thyroid hormone metabolism, abnormal Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thyroid hormone metabolism, abnormal phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Debrisoquine, poor metabolism of Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Debrisoquine, poor metabolism of phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Surfactant metabolism dysfunction, pulmonary, 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Surfactant metabolism dysfunction, pulmonary, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Megaloblastic anemia due to inborn errors of metabolism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Megaloblastic anemia due to inborn errors of metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Surfactant metabolism dysfunction, pulmonary, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Surfactant metabolism dysfunction, pulmonary, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Surfactant metabolism dysfunction, pulmonary, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Surfactant metabolism dysfunction, pulmonary, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Surfactant metabolism dysfunction, pulmonary, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Surfactant metabolism dysfunction, pulmonary, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Surfactant metabolism dysfunction, pulmonary, 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Surfactant metabolism dysfunction, pulmonary, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Homocystinuria-Megaloblastic anemia due to defect in cobalamin metabolism, cblE complementation type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the THIAMINE METABOLISM DYSFUNCTION SYNDROME 5 (EPISODIC ENCEPHALOPATHY TYPE) phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mephenytoin, poor metabolism of Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mephenytoin, poor metabolism of phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Drug Metabolism, Poor, CYP2D6-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Drug Metabolism, Poor, CYP2D6-Related from the curated CTD Gene-Disease Associations dataset.

Drug Metabolism, Poor, CYP2C19-Related Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Drug Metabolism, Poor, CYP2C19-Related from the curated CTD Gene-Disease Associations dataset.

Lipid Metabolism, Inborn Errors Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lipid Metabolism, Inborn Errors from the curated CTD Gene-Disease Associations dataset.

Pyruvate Metabolism, Inborn Errors Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pyruvate Metabolism, Inborn Errors from the curated CTD Gene-Disease Associations dataset.

Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Homocystinuria-Megaloblastic Anemia due to Defect in Cobalamin Metabolism, CblE Complementation Type from the curated CTD Gene-Disease Associations dataset.

Iron Metabolism Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Iron Metabolism Disorders from the curated CTD Gene-Disease Associations dataset.

Metabolism, Inborn Errors Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Metabolism, Inborn Errors from the curated CTD Gene-Disease Associations dataset.

Purine-Pyrimidine Metabolism, Inborn Errors Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Purine-Pyrimidine Metabolism, Inborn Errors from the curated CTD Gene-Disease Associations dataset.

Thyroid Hormone Metabolism, Abnormal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thyroid Hormone Metabolism, Abnormal from the curated CTD Gene-Disease Associations dataset.

Lipid Metabolism Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lipid Metabolism Disorders from the curated CTD Gene-Disease Associations dataset.

Amino Acid Metabolism, Inborn Errors Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amino Acid Metabolism, Inborn Errors from the curated CTD Gene-Disease Associations dataset.

Surfactant Metabolism Dysfunction, Pulmonary, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Surfactant Metabolism Dysfunction, Pulmonary, 1 from the curated CTD Gene-Disease Associations dataset.

Surfactant Metabolism Dysfunction, Pulmonary, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Surfactant Metabolism Dysfunctio