Name

Myasthenic syndrome, slow-channel congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, slow-channel congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

myasthenic syndrome, slow-channel congenital Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenic syndrome, slow-channel congenital phenotype from the curated OMIM Gene-Disease Associations dataset.

Myasthenic syndrome, congenital, postsynaptic slow-channel Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myasthenic syndrome, congenital, postsynaptic slow-channel from the curated CTD Gene-Disease Associations dataset.

Myasthenic syndrome, congenital, fast-channel Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, congenital, fast-channel phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myasthenic Syndrome, Congenital, Fast-Channel Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myasthenic Syndrome, Congenital, Fast-Channel from the curated CTD Gene-Disease Associations dataset.

myasthenic syndrome, fast-channel congenital Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenic syndrome, fast-channel congenital phenotype from the curated OMIM Gene-Disease Associations dataset.

Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myasthenic syndrome, congenital, with tubular aggregates 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, congenital, with tubular aggregates 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital myasthenic syndrome, acetazolamide-responsive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital myasthenic syndrome, acetazolamide-responsive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital myasthenic syndrome with episodic apnea Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital myasthenic syndrome with episodic apnea from the curated CTD Gene-Disease Associations dataset.

Congenital myasthenic syndrome ib Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital myasthenic syndrome ib from the curated CTD Gene-Disease Associations dataset.

MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY from the curated CTD Gene-Disease Associations dataset.

congenital myasthenic syndrome Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

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

congenital myasthenic syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

myasthenic syndrome, congenital, associated with facial dysmorphism and acetylcholine receptor deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenic syndrome, congenital, associated with facial dysmorphism and acetylcholine receptor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

myasthenic syndrome, congenital, with pre- and postsynaptic defects Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenic syndrome, congenital, with pre- and postsynaptic defects phenotype from the curated OMIM Gene-Disease Associations dataset.

myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

myasthenic syndrome, congenital, with tubular aggregates 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenic syndrome, congenital, with tubular aggregates 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy phenotype from the curated OMIM Gene-Disease Associations dataset.

myasthenic syndrome, congenital, associated with episodic apnea Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenic syndrome, congenital, associated with episodic apnea phenotype from the curated OMIM Gene-Disease Associations dataset.

Defective ALG14 causes congenital myasthenic syndrome (ALG14-CMS) Gene Set

From Reactome Pathways

proteins participating in the Defective ALG14 causes congenital myasthenic syndrome (ALG14-CMS) pathway from the Reactome Pathways dataset.

Myasthenic Syndromes, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myasthenic Syndromes, Congenital from the curated CTD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acne vulgaris; adrenal hyperplasia, congenital; congenital adrenal hyperplasia; hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; digeorge syndrome; heart defects, congenital; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lambert-eaton myasthenic syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

lung cancer; lambert-eaton myasthenic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lung cancer; lambert-eaton myasthenic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Lambert-Eaton Myasthenic Syndrome Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

myasthenic syndrome, acetazolamide-responsive Gene Set

From OMIM Gene-Disease Associations

genes associated with the myasthenic syndrome, acetazolamide-responsive phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; syndrome Gene Set

From GAD Gene-Disease Associations

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

birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; congenital abnormalities; heart defects, congenital; postoperative complications; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; down syndrome; heart defects, congenital; heart septal defects Gene Set

From GAD Gene-Disease Associations

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

abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; coloboma; congenital heart defects; disease models, animal; facial paralysis; heart defects, congenital; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aortic coarctation; aortic valve stenosis; congenital heart defects; discrete subaortic stenosis; heart defects, congenital; hypoplastic left heart syndrome; pulmonary valve stenosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hs4 enhancer complex (slow migrating complex) Gene Set

From CORUM Protein Complexes

proteins in the hs4 enhancer complex (slow migrating complex) protein complex from the CORUM Protein Complexes dataset.

slow coronary flow Gene Set

From GAD Gene-Disease Associations

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

slow Gene Set

From GeneRIF Biological Term Annotations

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

slow endocytic recycling Gene Set

From GO Biological Process Annotations

genes participating in the slow endocytic recycling biological process from the curated GO Biological Process Annotations dataset.

transition between fast and slow fiber Gene Set

From GO Biological Process Annotations

genes participating in the transition between fast and slow fiber biological process from the curated GO Biological Process Annotations dataset.

transition between slow and fast fiber Gene Set

From GO Biological Process Annotations

genes participating in the transition between slow and fast fiber biological process from the curated GO Biological Process Annotations dataset.

slow-twitch skeletal muscle fiber contraction Gene Set

From GO Biological Process Annotations

genes participating in the slow-twitch skeletal muscle fiber contraction biological process from the curated GO Biological Process Annotations dataset.

eeg with abnormally slow frequencies Gene Set

From HPO Gene-Disease Associations

genes associated with the eeg with abnormally slow frequencies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

slow saccadic eye movements Gene Set

From HPO Gene-Disease Associations

genes associated with the slow saccadic eye movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

slow-growing hair Gene Set

From HPO Gene-Disease Associations

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

eeg with generalized slow activity Gene Set

From HPO Gene-Disease Associations

genes associated with the eeg with generalized slow activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

slow decrease in visual acuity Gene Set

From HPO Gene-Disease Associations

genes associated with the slow decrease in visual acuity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

osteomyelitis leading to amputation due to slow healing fractures Gene Set

From HPO Gene-Disease Associations

genes associated with the osteomyelitis leading to amputation due to slow healing fractures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

slow progression Gene Set

From HPO Gene-Disease Associations

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

slow postnatal weight gain Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the slow postnatal weight gain phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

slow aging Gene Set

From MPO Gene-Phenotype Associations

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

slow extinction of fear memory Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the slow extinction of fear memory phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

slow wallerian degeneration Gene Set

From MPO Gene-Phenotype Associations

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

{aids, slow progression to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {aids, slow progression to} phenotype from the curated OMIM Gene-Disease Associations dataset.

[acetylation, slow] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [acetylation, slow] phenotype from the curated OMIM Gene-Disease Associations dataset.

slow muscle Gene Set

From TISSUES Curated Tissue Protein Expression Evidence Scores

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

slow twitch muscle fiber Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue slow twitch muscle fiber in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

slow muscle Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

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

myasthenic Gene Set

From GeneRIF Biological Term Annotations

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

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

From GAD Gene-Disease Associations

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

abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, multiple; heart defects, congenital; leopard syndrome; noonan syndrome; skin abnormalities in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

meckel-gruber syndrome; abnormalities, multiple; congenital abnormalities; polydactyly; syndrome Gene Set

From GAD Gene-Disease Associations

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

atrial septal defects; cardiomyopathy, dilated; congenital heart defects; dcm - dilated cardiomyopathy; heart defects, congenital; heart septal defects, atrial Gene Set

From GAD Gene-Disease Associations

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

congenital heart defects; folic acid deficiency; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

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

adrenal hyperplasia, congenital; congenital adrenal hyperplasia Gene Set

From GAD Gene-Disease Associations

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

congenital heart defects; heart defects, congenital; obesity Gene Set

From GAD Gene-Disease Associations

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

congenital heart defects; coronary disease; coronary heart disease; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

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

cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cleft lip; cleft palate; congenital heart defects; heart defects, congenital; hyperhomocysteinemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adrenal hyperplasia, congenital; cardiovascular diseases; congenital adrenal hyperplasia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal hyperplasia, congenital; cardiovascular diseases; congenital adrenal hyperplasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

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

congenital heart defects; heart defects, congenital; ventricular outflow obstruction Gene Set

From GAD Gene-Disease Associations

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

congenital heart defects; heart defects, congenital; nervous system diseases Gene Set

From GAD Gene-Disease Associations

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

atrial septal defects; congenital heart defects; heart defects, congenital; heart septal defects, atrial; heart septal defects, ventricular; ventricular septal defects Gene Set

From GAD Gene-Disease Associations

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

body weight; congenital heart defects; growth disorders; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; congenital heart defects; growth disorders; heart defects, congenital in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot Gene Set

From GAD Gene-Disease Associations

genes associated with the disease congenital heart defects; heart defects, congenital; heart septal defects; tetralogy of fallot in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adrenal hyperplasia, congenital; congenital adrenal hyperplasia; virilism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adrenal hyperplasia, congenital; congenital adrenal hyperplasia; virilism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Lynch syndrome:Lynch syndrome:Lynch syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

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

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

Lethal congenital contracture syndrome 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lethal congenital contracture syndrome 5 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.

Lethal congenital contractural syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lethal congenital contractural syndrome 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple congenital anomalies-hypotonia-seizures syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Rett syndrome, congenital variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Rett syndrome, congenital variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Finnish congenital nephrotic syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Finnish congenital nephrotic syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lethal congenital contracture syndrome 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lethal congenital contracture syndrome 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital long QT syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set

From ClinVar Gene-Phenotype Associations

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

Multiple congenital anomalies-hypotonia-seizures syndrome 3 Gene Set

From ClinVar Gene-Phenotype Associations

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

Congenital muscular hypertrophy-cerebral syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular hypertrophy-cerebral syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lethal Congenital Contracture Syndrome 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lethal Congenital Contracture Syndrome 2 from the curated CTD Gene-Disease Associations dataset.

Congenital central hypoventilation syndrome Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital central hypoventilation syndrome from the curated CTD Gene-Disease Associations dataset.

Lethal congenital contracture syndrome 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lethal congenital contracture syndrome 1 from the curated CTD Gene-Disease Associations dataset.

RETT SYNDROME, CONGENITAL VARIANT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease RETT SYNDROME, CONGENITAL VARIANT from the curated CTD Gene-Disease Associations dataset.

Lethal Congenital Contractural Syndrome 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lethal Congenital Contractural Syndrome 3 from the curated CTD Gene-Disease Associations dataset.

retinitis pigmentosa; leber congenital amaurosis; usher syndrome type i Gene Set

From GAD Gene-Disease Associations

genes associated with the disease retinitis pigmentosa; leber congenital amaurosis; usher syndrome type i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

congenital central hypoventilation syndrome Gene Set

From GAD Gene-Disease Associations

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

limb deformities, congenital; rothmund-thomson syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease limb deformities, congenital; rothmund-thomson syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

down syndrome; heart defects, congenital Gene Set

From GAD Gene-Disease Associations

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

abnormalities, multiple; ectodermal dysplasia; heart defects, congenital; mental retardation; syndrome Gene Set

From GAD Gene-Disease Associations

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

congenital sick sinus syndrome Gene Set

From GAD Gene-Disease Associations

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

down syndrome; heart defects, congenital; hypertension, pulmonary Gene Set

From GAD Gene-Disease Associations

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

congenital nephrotic syndrome Gene Set

From HPO Gene-Disease Associations

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

rett syndrome, congenital variant Gene Set

From OMIM Gene-Disease Associations

genes associated with the rett syndrome, congenital variant phenotype from the curated OMIM Gene-Disease Associations dataset.

central hypoventilation syndrome, congenital, with or without hirschsprung disease Gene Set

From OMIM Gene-Disease Associations

genes associated with the central hypoventilation syndrome, congenital, with or without hirschsprung disease phenotype from the curated OMIM Gene-Disease Associations dataset.

lethal congenital contracture syndrome 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the lethal congenital contracture syndrome 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

lethal congenital contracture syndrome 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the lethal congenital contracture syndrome 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

lethal congenital contracture syndrome 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the lethal congenital contracture syndrome 1 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.

interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital Gene Set

From OMIM Gene-Disease Associations

genes associated with the interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital phenotype from the curated OMIM Gene-Disease Associations dataset.

central hypoventilation syndrome, congenital Gene Set

From OMIM Gene-Disease Associations

genes associated with the central hypoventilation syndrome, congenital phenotype from the curated OMIM Gene-Disease Associations dataset.

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

From OMIM Gene-Disease Associations

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

multiple congenital anomalies-hypotonia-seizures syndrome 1 Gene Set

From OMIM Gene-Disease Associations

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

multiple congenital anomalies-hypotonia-seizures syndrome 2 Gene Set

From OMIM Gene-Disease Associations

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

melanocytic nevus syndrome, congenital, somatic Gene Set

From OMIM Gene-Disease Associations

genes associated with the melanocytic nevus syndrome, congenital, somatic phenotype from the curated OMIM Gene-Disease Associations dataset.

lethal congenital contractural syndrome 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the lethal congenital contractural syndrome 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

lethal congenital contractural syndrome 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the lethal congenital contractural syndrome 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

?partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

potassium channel complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the potassium channel complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

voltage-gated sodium channel complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the voltage-gated sodium channel complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

ion channel complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the ion channel complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

chloride channel complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the chloride channel complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

atp-sensitive potassium channel complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the atp-sensitive potassium channel complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

intracellular cyclic nucleotide activated cation channel complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the intracellular cyclic nucleotide activated cation channel complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

voltage-gated calcium channel complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the voltage-gated calcium channel complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

voltage-gated potassium channel complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the voltage-gated potassium channel complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

acetylcholine-gated channel complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the acetylcholine-gated channel complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

sodium channel complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the sodium channel complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

calcium channel complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the calcium channel complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

cation channel complex Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the cation channel complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

nuclear pore central transport channel Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the nuclear pore central transport channel cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

voltage-gated sodium channel complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the voltage-gated sodium channel complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

atp-sensitive potassium channel complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the atp-sensitive potassium channel complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

potassium channel complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the potassium channel complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

ion channel complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the ion channel complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

chloride channel complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the chloride channel complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

glycine-gated chloride channel complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the glycine-gated chloride channel complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

voltage-gated calcium channel complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the voltage-gated calcium channel complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

voltage-gated potassium channel complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the voltage-gated potassium channel complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

acetylcholine-gated channel complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the acetylcholine-gated channel complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

sodium channel complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the sodium channel complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

calcium channel complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the calcium channel complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

cation channel complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the cation channel complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

TRPC3-TRPC4 channel complex, redox-sensitive Gene Set

From CORUM Protein Complexes

proteins in the TRPC3-TRPC4 channel complex, redox-sensitive protein complex from the CORUM Protein Complexes dataset.

Nogo-potassium channel complex Gene Set

From CORUM Protein Complexes

proteins in the Nogo-potassium channel complex protein complex from the CORUM Protein Complexes dataset.

Channel complex TRPM6-TRPM7 Gene Set

From CORUM Protein Complexes

proteins in the Channel complex TRPM6-TRPM7 protein complex from the CORUM Protein Complexes dataset.

Kv4.2-DPP10 channel complex Gene Set

From CORUM Protein Complexes

proteins in the Kv4.2-DPP10 channel complex protein complex from the CORUM Protein Complexes dataset.

Calcium Channel Blockers Gene Set

From CTD Gene-Chemical Interactions

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

channel Gene Set

From GeneRIF Biological Term Annotations

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

regulation of high voltage-gated calcium channel activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of high voltage-gated calcium channel activity biological process from the curated GO Biological Process Annotations dataset.

regulation of acid-sensing ion channel activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of acid-sensing ion channel activity biological process from the curated GO Biological Process Annotations dataset.

positive regulation of ryanodine-sensitive calcium-release channel activity by adrenergic receptor signaling pathway involved in positive regulation of cardiac muscle contraction Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of ryanodine-sensitive calcium-release channel activity by adrenergic receptor signaling pathway involved in positive regulation of cardiac muscle contraction biological process from the curated GO Biological Process Annotations dataset.

negative regulation of ryanodine-sensitive calcium-release channel activity Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of ryanodine-sensitive calcium-release channel activity biological process from the curated GO Biological Process Annotations dataset.

regulation of cation channel activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cation channel activity biological process from the curated GO Biological Process Annotations dataset.

skeletal muscle acetylcholine-gated channel clustering Gene Set

From GO Biological Process Annotations

genes participating in the skeletal muscle acetylcholine-gated channel clustering biological process from the curated GO Biological Process Annotations dataset.

neurotransmitter-gated ion channel clustering Gene Set

From GO Biological Process Annotations

genes participating in the neurotransmitter-gated ion channel clustering biological process from the curated GO Biological Process Annotations dataset.

regulation of intracellular calcium activated chloride channel activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of intracellular calcium activated chloride channel activity biological process from the curated GO Biological Process Annotations dataset.

activation of store-operated calcium channel activity Gene Set

From GO Biological Process Annotations

genes participating in the activation of store-operated calcium channel activity biological process from the curated GO Biological Process Annotations dataset.

positive regulation of voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization biological process from the curated GO Biological Process Annotations dataset.

neuronal ion channel clustering Gene Set

From GO Biological Process Annotations

genes participating in the neuronal ion channel clustering biological process from the curated GO Biological Process Annotations dataset.

positive regulation of large conductance calcium-activated potassium channel activity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of large conductance calcium-activated potassium channel activity biological process from the curated GO Biological Process Annotations dataset.

regulation of voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization Gene Set

From GO Biological Process Annotations

genes participating in the regulation of voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization biological process from the curated GO Biological Process Annotations dataset.

positive regulation of voltage-gated chloride channel activity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of voltage-gated chloride channel activity biological process from the curated GO Biological Process Annotations dataset.

positive regulation of ryanodine-sensitive calcium-release channel activity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of ryanodine-sensitive calcium-release channel activity biological process from the curated GO Biological Process Annotations dataset.

positive regulation of store-operated calcium channel activity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of store-operated calcium channel activity biological process from the curated GO Biological Process Annotations dataset.

positive regulation of inositol 1,4,5-trisphosphate-sensitive calcium-release channel activity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of inositol 1,4,5-trisphosphate-sensitive calcium-release channel activity biological process from the curated GO Biological Process Annotations dataset.

regulation of ryanodine-sensitive calcium-release channel activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of ryanodine-sensitive calcium-release channel activity biological process from the curated GO Biological Process Annotations dataset.

positive regulation of voltage-gated calcium channel activity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of voltage-gated calcium channel activity biological process from the curated GO Biological Process Annotations dataset.

negative regulation of intracellular calcium activated chloride channel activity Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of intracellular calcium activated chloride channel activity biological process from the curated GO Biological Process Annotations dataset.

negative regulation of cation channel activity Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of cation channel activity biological process from the curated GO Biological Process Annotations dataset.

regulation of cyclic nucleotide-gated ion channel activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of cyclic nucleotide-gated ion channel activity biological process from the curated GO Biological Process Annotations dataset.

regulation of inward rectifier potassium channel activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of inward rectifier potassium channel activity biological process from the curated GO Biological Process Annotations dataset.

regulation of g-protein activated inward rectifier potassium channel activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of g-protein activated inward rectifier potassium channel activity biological process from the curated GO Biological Process Annotations dataset.

regulation of store-operated calcium channel activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of store-operated calcium channel activity biological process from the curated GO Biological Process Annotations dataset.

regulation of voltage-gated calcium channel activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of voltage-gated calcium channel activity biological process from the curated GO Biological Process Annotations dataset.

regulation of delayed rectifier potassium channel activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of delayed rectifier potassium channel activity biological process from the curated GO Biological Process Annotations dataset.

regulation of inositol 1,4,5-trisphosphate-sensitive calcium-release channel activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of inositol 1,4,5-trisphosphate-sensitive calcium-release channel activity biological process from the curated GO Biological Process Annotations dataset.

positive regulation of delayed rectifier potassium channel activity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of delayed rectifier potassium channel activity biological process from the curated GO Biological Process Annotations dataset.

regulation of anion channel activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of anion channel activity biological process from the curated GO Biological Process Annotations dataset.

negative regulation of voltage-gated calcium channel activity Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of voltage-gated calcium channel activity biological process from the curated GO Biological Process Annotations dataset.

negative regulation of voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization biological process from the curated GO Biological Process Annotations dataset.

regulation of voltage-gated chloride channel activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of voltage-gated chloride channel activity biological process from the curated GO Biological Process Annotations dataset.

regulation of large conductance calcium-activated potassium channel activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of large conductance calcium-activated potassium channel activity biological process from the curated GO Biological Process Annotations dataset.

negative regulation of anion channel activity Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of anion channel activity biological process from the curated GO Biological Process Annotations dataset.

negative regulation of delayed rectifier potassium channel activity Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of delayed rectifier potassium channel activity biological process from the curated GO Biological Process Annotations dataset.

positive regulation of anion channel activity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of anion channel activity biological process from the curated GO Biological Process Annotations dataset.

negative regulation of voltage-gated potassium channel activity Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of voltage-gated potassium channel activity biological process from the curated GO Biological Process Annotations dataset.

positive regulation of voltage-gated potassium channel activity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of voltage-gated potassium channel activity biological process from the curated GO Biological Process Annotations dataset.

positive regulation of cation channel activity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of cation channel activity biological process from the curated GO Biological Process Annotations dataset.

potassium channel complex Gene Set

From GO Cellular Component Annotations

proteins localized to the potassium channel complex cellular component from the curated GO Cellular Component Annotations dataset.

atp-sensitive potassium channel complex Gene Set

From GO Cellular Component Annotations

proteins localized to the atp-sensitive potassium channel complex cellular component from the curated GO Cellular Component Annotations dataset.

ion channel complex Gene Set

From GO Cellular Component Annotations

proteins localized to the ion channel complex cellular component from the curated GO Cellular Component Annotations dataset.

chloride channel complex Gene Set

From GO Cellular Component Annotations

proteins localized to the chloride channel complex cellular component from the curated GO Cellular Component Annotations dataset.

inward rectifier potassium channel complex Gene Set

From GO Cellular Component Annotations

proteins localized to the inward rectifier potassium channel complex cellular component from the curated GO Cellular Component Annotations dataset.

intracellular cyclic nucleotide activated cation channel complex Gene Set

From GO Cellular Component Annotations

proteins localized to the intracellular cyclic nucleotide activated cation channel complex cellular component from the curated GO Cellular Component Annotations dataset.

l-type voltage-gated calcium channel complex Gene Set

From GO Cellular Component Annotations

proteins localized to the l-type voltage-gated calcium channel complex cellular component from the curated GO Cellular Component Annotations dataset.

voltage-gated calcium channel complex Gene Set

From GO Cellular Component Annotations

proteins localized to the voltage-gated calcium channel complex cellular component from the curated GO Cellular Component Annotations dataset.

voltage-gated potassium channel complex Gene Set

From GO Cellular Component Annotations

proteins localized to the voltage-gated potassium channel complex cellular component from the curated GO Cellular Component Annotations dataset.

acetylcholine-gated channel complex Gene Set

From GO Cellular Component Annotations

proteins localized to the acetylcholine-gated channel complex cellular component from the curated GO Cellular Component Annotations dataset.

sodium channel complex Gene Set

From GO Cellular Component Annotations

proteins localized to the sodium channel complex cellular component from the curated GO Cellular Component Annotations dataset.

voltage-gated sodium channel complex Gene Set

From GO Cellular Component Annotations

proteins localized to the voltage-gated sodium channel complex cellular component from the curated GO Cellular Component Annotations dataset.

calcium channel complex Gene Set

From GO Cellular Component Annotations

proteins localized to the calcium channel complex cellular component from the curated GO Cellular Component Annotations dataset.

cation channel complex Gene Set

From GO Cellular Component Annotations

proteins localized to the cation channel complex cellular component from the curated GO Cellular Component Annotations dataset.

inositol 1,4,5-trisphosphate-sensitive calcium-release channel activity Gene Set

From GO Molecular Function Annotations

genes performing the inositol 1,4,5-trisphosphate-sensitive calcium-release channel activity molecular function from the curated GO Molecular Function Annotations dataset.

large conductance calcium-activated potassium channel activity Gene Set

From GO Molecular Function Annotations

genes performing the large conductance calcium-activated potassium channel activity molecular function from the curated GO Molecular Function Annotations dataset.

intracellular calcium activated chloride channel activity Gene Set

From GO Molecular Function Annotations

genes performing the intracellular calcium activated chloride channel activity molecular function from the curated GO Molecular Function Annotations dataset.

atp-activated inward rectifier potassium channel activity Gene Set

From GO Molecular Function Annotations

genes performing the atp-activated inward rectifier potassium channel activity molecular function from the curated GO Molecular Function Annotations dataset.

chloride channel activity Gene Set

From GO Molecular Function Annotations

genes performing the chloride channel activity molecular function from the curated GO Molecular Function Annotations dataset.

atp-binding and phosphorylation-dependent chloride channel activity Gene Set

From GO Molecular Function Annotations

genes performing the atp-binding and phosphorylation-dependent chloride channel activity molecular function from the curated GO Molecular Function Annotations dataset.

intracellular camp activated cation channel activity Gene Set

From GO Molecular Function Annotations

genes performing the intracellular camp activated cation channel activity molecular function from the curated GO Molecular Function Annotations dataset.

voltage-gated potassium channel activity involved in sa node cell action potential repolarization Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated potassium channel activity involved in sa node cell action potential repolarization molecular function from the curated GO Molecular Function Annotations dataset.

temperature-gated ion channel activity Gene Set

From GO Molecular Function Annotations

genes performing the temperature-gated ion channel activity molecular function from the curated GO Molecular Function Annotations dataset.

wide pore channel activity Gene Set

From GO Molecular Function Annotations

genes performing the wide pore channel activity molecular function from the curated GO Molecular Function Annotations dataset.

voltage-gated sodium channel activity involved in cardiac muscle cell action potential Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated sodium channel activity involved in cardiac muscle cell action potential molecular function from the curated GO Molecular Function Annotations dataset.

gap junction hemi-channel activity Gene Set

From GO Molecular Function Annotations

genes performing the gap junction hemi-channel activity molecular function from the curated GO Molecular Function Annotations dataset.

gap junction channel activity Gene Set

From GO Molecular Function Annotations

genes performing the gap junction channel activity molecular function from the curated GO Molecular Function Annotations dataset.

inhibitory extracellular ligand-gated ion channel activity Gene Set

From GO Molecular Function Annotations

genes performing the inhibitory extracellular ligand-gated ion channel activity molecular function from the curated GO Molecular Function Annotations dataset.

voltage-gated sodium channel activity Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated sodium channel activity molecular function from the curated GO Molecular Function Annotations dataset.

high voltage-gated calcium channel activity Gene Set

From GO Molecular Function Annotations

genes performing the high voltage-gated calcium channel activity molecular function from the curated GO Molecular Function Annotations dataset.

channel activity Gene Set

From GO Molecular Function Annotations

genes performing the channel activity molecular function from the curated GO Molecular Function Annotations dataset.

calcium channel regulator activity Gene Set

From GO Molecular Function Annotations

genes performing the calcium channel regulator activity molecular function from the curated GO Molecular Function Annotations dataset.

outward rectifier potassium channel activity Gene Set

From GO Molecular Function Annotations

genes performing the outward rectifier potassium channel activity molecular function from the curated GO Molecular Function Annotations dataset.

cation channel activity Gene Set

From GO Molecular Function Annotations

genes performing the cation channel activity molecular function from the curated GO Molecular Function Annotations dataset.

potassium ion leak channel activity Gene Set

From GO Molecular Function Annotations

genes performing the potassium ion leak channel activity molecular function from the curated GO Molecular Function Annotations dataset.

open rectifier potassium channel activity Gene Set

From GO Molecular Function Annotations

genes performing the open rectifier potassium channel activity molecular function from the curated GO Molecular Function Annotations dataset.

ion channel binding Gene Set

From GO Molecular Function Annotations

genes performing the ion channel binding molecular function from the curated GO Molecular Function Annotations dataset.

delayed rectifier potassium channel activity Gene Set

From GO Molecular Function Annotations

genes performing the delayed rectifier potassium channel activity molecular function from the curated GO Molecular Function Annotations dataset.

ryanodine-sensitive calcium-release channel activity Gene Set

From GO Molecular Function Annotations

genes performing the ryanodine-sensitive calcium-release channel activity molecular function from the curated GO Molecular Function Annotations dataset.

voltage-gated sodium channel activity involved in sa node cell action potential Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated sodium channel activity involved in sa node cell action potential molecular function from the curated GO Molecular Function Annotations dataset.

calcium-activated potassium channel activity Gene Set

From GO Molecular Function Annotations

genes performing the calcium-activated potassium channel activity molecular function from the curated GO Molecular Function Annotations dataset.

extracellular-glycine-gated chloride channel activity Gene Set

From GO Molecular Function Annotations

genes performing the extracellular-glycine-gated chloride channel activity molecular function from the curated GO Molecular Function Annotations dataset.

small conductance calcium-activated potassium channel activity Gene Set

From GO Molecular Function Annotations

genes performing the small conductance calcium-activated potassium channel activity molecular function from the curated GO Molecular Function Annotations dataset.

voltage-gated chloride channel activity Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated chloride channel activity molecular function from the curated GO Molecular Function Annotations dataset.

atp-gated ion channel activity Gene Set

From GO Molecular Function Annotations

genes performing the atp-gated ion channel activity molecular function from the curated GO Molecular Function Annotations dataset.

leak channel activity Gene Set

From GO Molecular Function Annotations

genes performing the leak channel activity molecular function from the curated GO Molecular Function Annotations dataset.

calcium activated cation channel activity Gene Set

From GO Molecular Function Annotations

genes performing the calcium activated cation channel activity molecular function from the curated GO Molecular Function Annotations dataset.

voltage-gated potassium channel activity involved in cardiac muscle cell action potential repolarization Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated potassium channel activity involved in cardiac muscle cell action potential repolarization molecular function from the curated GO Molecular Function Annotations dataset.

voltage-gated calcium channel activity involved sa node cell action potential Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated calcium channel activity involved sa node cell action potential molecular function from the curated GO Molecular Function Annotations dataset.

voltage-gated proton channel activity Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated proton channel activity molecular function from the curated GO Molecular Function Annotations dataset.

extracellular ligand-gated ion channel activity Gene Set

From GO Molecular Function Annotations

genes performing the extracellular ligand-gated ion channel activity molecular function from the curated GO Molecular Function Annotations dataset.

voltage-gated sodium channel activity involved in av node cell action potential Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated sodium channel activity involved in av node cell action potential molecular function from the curated GO Molecular Function Annotations dataset.

transmitter-gated ion channel activity Gene Set

From GO Molecular Function Annotations

genes performing the transmitter-gated ion channel activity molecular function from the curated GO Molecular Function Annotations dataset.

store-operated calcium channel activity Gene Set

From GO Molecular Function Annotations

genes performing the store-operated calcium channel activity molecular function from the curated GO Molecular Function Annotations dataset.

channel-conductance-controlling atpase activity Gene Set

From GO Molecular Function Annotations

genes performing the channel-conductance-controlling atpase activity molecular function from the curated GO Molecular Function Annotations dataset.

hydrogen ion channel activity Gene Set

From GO Molecular Function Annotations

genes performing the hydrogen ion channel activity molecular function from the curated GO Molecular Function Annotations dataset.

ion channel inhibitor activity Gene Set

From GO Molecular Function Annotations

genes performing the ion channel inhibitor activity molecular function from the curated GO Molecular Function Annotations dataset.

g-protein activated inward rectifier potassium channel activity Gene Set

From GO Molecular Function Annotations

genes performing the g-protein activated inward rectifier potassium channel activity molecular function from the curated GO Molecular Function Annotations dataset.

intracellular cyclic nucleotide activated cation channel activity Gene Set

From GO Molecular Function Annotations

genes performing the intracellular cyclic nucleotide activated cation channel activity molecular function from the curated GO Molecular Function Annotations dataset.

volume-sensitive chloride channel activity Gene Set

From GO Molecular Function Annotations

genes performing the volume-sensitive chloride channel activity molecular function from the curated GO Molecular Function Annotations dataset.

anion channel activity Gene Set

From GO Molecular Function Annotations

genes performing the anion channel activity molecular function from the curated GO Molecular Function Annotations dataset.

potassium channel inhibitor activity Gene Set

From GO Molecular Function Annotations

genes performing the potassium channel inhibitor activity molecular function from the curated GO Molecular Function Annotations dataset.

water channel activity Gene Set

From GO Molecular Function Annotations

genes performing the water channel activity molecular function from the curated GO Molecular Function Annotations dataset.

acetylcholine-activated cation-selective channel activity Gene Set

From GO Molecular Function Annotations

genes performing the acetylcholine-activated cation-selective channel activity molecular function from the curated GO Molecular Function Annotations dataset.

voltage-gated channel activity Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated channel activity molecular function from the curated GO Molecular Function Annotations dataset.

intracellular ligand-gated ion channel activity Gene Set

From GO Molecular Function Annotations

genes performing the intracellular ligand-gated ion channel activity molecular function from the curated GO Molecular Function Annotations dataset.

voltage-gated potassium channel activity involved in bundle of his cell action potential repolarization Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated potassium channel activity involved in bundle of his cell action potential repolarization molecular function from the curated GO Molecular Function Annotations dataset.

low voltage-gated calcium channel activity Gene Set

From GO Molecular Function Annotations

genes performing the low voltage-gated calcium channel activity molecular function from the curated GO Molecular Function Annotations dataset.

cyclic nucleotide-gated ion channel activity Gene Set

From GO Molecular Function Annotations

genes performing the cyclic nucleotide-gated ion channel activity molecular function from the curated GO Molecular Function Annotations dataset.

ion channel activity Gene Set

From GO Molecular Function Annotations

genes performing the ion channel activity molecular function from the curated GO Molecular Function Annotations dataset.

ion gated channel activity Gene Set

From GO Molecular Function Annotations

genes performing the ion gated channel activity molecular function from the curated GO Molecular Function Annotations dataset.

channel inhibitor activity Gene Set

From GO Molecular Function Annotations

genes performing the channel inhibitor activity molecular function from the curated GO Molecular Function Annotations dataset.

extracellular-glycine-gated ion channel activity Gene Set

From GO Molecular Function Annotations

genes performing the extracellular-glycine-gated ion channel activity molecular function from the curated GO Molecular Function Annotations dataset.

sodium channel activity Gene Set

From GO Molecular Function Annotations

genes performing the sodium channel activity molecular function from the curated GO Molecular Function Annotations dataset.

acid-sensing ion channel activity Gene Set

From GO Molecular Function Annotations

genes performing the acid-sensing ion channel activity molecular function from the curated GO Molecular Function Annotations dataset.

ligand-gated ion channel activity Gene Set

From GO Molecular Function Annotations

genes performing the ligand-gated ion channel activity molecular function from the curated GO Molecular Function Annotations dataset.

ligand-gated channel activity Gene Set

From GO Molecular Function Annotations

genes performing the ligand-gated channel activity molecular function from the curated GO Molecular Function Annotations dataset.

voltage-gated anion channel activity Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated anion channel activity molecular function from the curated GO Molecular Function Annotations dataset.

chloride channel inhibitor activity Gene Set

From GO Molecular Function Annotations

genes performing the chloride channel inhibitor activity molecular function from the curated GO Molecular Function Annotations dataset.

sodium channel regulator activity Gene Set

From GO Molecular Function Annotations

genes performing the sodium channel regulator activity molecular function from the curated GO Molecular Function Annotations dataset.

mechanically-gated ion channel activity Gene Set

From GO Molecular Function Annotations

genes performing the mechanically-gated ion channel activity molecular function from the curated GO Molecular Function Annotations dataset.

gap junction channel activity involved in cell communication by electrical coupling Gene Set

From GO Molecular Function Annotations

genes performing the gap junction channel activity involved in cell communication by electrical coupling molecular function from the curated GO Molecular Function Annotations dataset.

intracellular cgmp activated cation channel activity Gene Set

From GO Molecular Function Annotations

genes performing the intracellular cgmp activated cation channel activity molecular function from the curated GO Molecular Function Annotations dataset.

excitatory extracellular ligand-gated ion channel activity Gene Set

From GO Molecular Function Annotations

genes performing the excitatory extracellular ligand-gated ion channel activity molecular function from the curated GO Molecular Function Annotations dataset.

gated channel activity Gene Set

From GO Molecular Function Annotations

genes performing the gated channel activity molecular function from the curated GO Molecular Function Annotations dataset.

voltage-gated sodium channel activity involved in purkinje myocyte action potential Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated sodium channel activity involved in purkinje myocyte action potential molecular function from the curated GO Molecular Function Annotations dataset.

sodium channel inhibitor activity Gene Set

From GO Molecular Function Annotations

genes performing the sodium channel inhibitor activity molecular function from the curated GO Molecular Function Annotations dataset.

a-type (transient outward) potassium channel activity Gene Set

From GO Molecular Function Annotations

genes performing the a-type (transient outward) potassium channel activity molecular function from the curated GO Molecular Function Annotations dataset.

temperature-gated cation channel activity Gene Set

From GO Molecular Function Annotations

genes performing the temperature-gated cation channel activity molecular function from the curated GO Molecular Function Annotations dataset.

protein channel activity Gene Set

From GO Molecular Function Annotations

genes performing the protein channel activity molecular function from the curated GO Molecular Function Annotations dataset.

gap junction channel activity involved in av node cell-bundle of his cell electrical coupling Gene Set

From GO Molecular Function Annotations

genes performing the gap junction channel activity involved in av node cell-bundle of his cell electrical coupling molecular function from the curated GO Molecular Function Annotations dataset.

voltage-gated calcium channel activity Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated calcium channel activity molecular function from the curated GO Molecular Function Annotations dataset.

calcium channel inhibitor activity Gene Set

From GO Molecular Function Annotations

genes performing the calcium channel inhibitor activity molecular function from the curated GO Molecular Function Annotations dataset.

extracellular-glutamate-gated ion channel activity Gene Set

From GO Molecular Function Annotations

genes performing the extracellular-glutamate-gated ion channel activity molecular function from the curated GO Molecular Function Annotations dataset.

voltage-gated cation channel activity Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated cation channel activity molecular function from the curated GO Molecular Function Annotations dataset.

voltage-gated ion channel activity Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated ion channel activity molecular function from the curated GO Molecular Function Annotations dataset.

inward rectifier potassium channel inhibitor activity Gene Set

From GO Molecular Function Annotations

genes performing the inward rectifier potassium channel inhibitor activity molecular function from the curated GO Molecular Function Annotations dataset.

potassium channel activity Gene Set

From GO Molecular Function Annotations

genes performing the potassium channel activity molecular function from the curated GO Molecular Function Annotations dataset.

chloride channel regulator activity Gene Set

From GO Molecular Function Annotations

genes performing the chloride channel regulator activity molecular function from the curated GO Molecular Function Annotations dataset.

voltage-gated potassium channel activity involved in atrial cardiac muscle cell action potential repolarization Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated potassium channel activity involved in atrial cardiac muscle cell action potential repolarization molecular function from the curated GO Molecular Function Annotations dataset.

voltage-gated sodium channel activity involved in bundle of his cell action potential Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated sodium channel activity involved in bundle of his cell action potential molecular function from the curated GO Molecular Function Annotations dataset.

extracellular atp-gated cation channel activity Gene Set

From GO Molecular Function Annotations

genes performing the extracellular atp-gated cation channel activity molecular function from the curated GO Molecular Function Annotations dataset.

gaba-gated chloride ion channel activity Gene Set

From GO Molecular Function Annotations

genes performing the gaba-gated chloride ion channel activity molecular function from the curated GO Molecular Function Annotations dataset.

acetylcholine-gated cation channel activity Gene Set

From GO Molecular Function Annotations

genes performing the acetylcholine-gated cation channel activity molecular function from the curated GO Molecular Function Annotations dataset.

intermediate conductance calcium-activated potassium channel activity Gene Set

From GO Molecular Function Annotations

genes performing the intermediate conductance calcium-activated potassium channel activity molecular function from the curated GO Molecular Function Annotations dataset.

voltage-gated calcium channel activity involved in cardiac muscle cell action potential Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated calcium channel activity involved in cardiac muscle cell action potential molecular function from the curated GO Molecular Function Annotations dataset.

volume-sensitive anion channel activity Gene Set

From GO Molecular Function Annotations

genes performing the volume-sensitive anion channel activity molecular function from the curated GO Molecular Function Annotations dataset.

serotonin-activated cation-selective channel activity Gene Set

From GO Molecular Function Annotations

genes performing the serotonin-activated cation-selective channel activity molecular function from the curated GO Molecular Function Annotations dataset.

substrate-specific channel activity Gene Set

From GO Molecular Function Annotations

genes performing the substrate-specific channel activity molecular function from the curated GO Molecular Function Annotations dataset.

urea channel activity Gene Set

From GO Molecular Function Annotations

genes performing the urea channel activity molecular function from the curated GO Molecular Function Annotations dataset.

naadp-sensitive calcium-release channel activity Gene Set

From GO Molecular Function Annotations

genes performing the naadp-sensitive calcium-release channel activity molecular function from the curated GO Molecular Function Annotations dataset.

glycerol channel activity Gene Set

From GO Molecular Function Annotations

genes performing the glycerol channel activity molecular function from the curated GO Molecular Function Annotations dataset.

inward rectifier potassium channel activity Gene Set

From GO Molecular Function Annotations

genes performing the inward rectifier potassium channel activity molecular function from the curated GO Molecular Function Annotations dataset.

channel regulator activity Gene Set

From GO Molecular Function Annotations

genes performing the channel regulator activity molecular function from the curated GO Molecular Function Annotations dataset.

calcium channel activity Gene Set

From GO Molecular Function Annotations

genes performing the calcium channel activity molecular function from the curated GO Molecular Function Annotations dataset.

calcium-release channel activity Gene Set

From GO Molecular Function Annotations

genes performing the calcium-release channel activity molecular function from the curated GO Molecular Function Annotations dataset.

mechanically gated channel activity Gene Set

From GO Molecular Function Annotations

genes performing the mechanically gated channel activity molecular function from the curated GO Molecular Function Annotations dataset.

narrow pore channel activity Gene Set

From GO Molecular Function Annotations

genes performing the narrow pore channel activity molecular function from the curated GO Molecular Function Annotations dataset.

intracellular ligand-gated calcium channel activity Gene Set

From GO Molecular Function Annotations

genes performing the intracellular ligand-gated calcium channel activity molecular function from the curated GO Molecular Function Annotations dataset.

voltage-gated potassium channel activity Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated potassium channel activity molecular function from the curated GO Molecular Function Annotations dataset.

transmitter-gated channel activity Gene Set

From GO Molecular Function Annotations

genes performing the transmitter-gated channel activity molecular function from the curated GO Molecular Function Annotations dataset.

gap junction channel activity involved in cardiac conduction electrical coupling Gene Set

From GO Molecular Function Annotations

genes performing the gap junction channel activity involved in cardiac conduction electrical coupling molecular function from the curated GO Molecular Function Annotations dataset.

ligand-gated sodium channel activity Gene Set

From GO Molecular Function Annotations

genes performing the ligand-gated sodium channel activity molecular function from the curated GO Molecular Function Annotations dataset.

voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization Gene Set

From GO Molecular Function Annotations

genes performing the voltage-gated potassium channel activity involved in ventricular cardiac muscle cell action potential repolarization molecular function from the curated GO Molecular Function Annotations dataset.

potassium channel regulator activity Gene Set

From GO Molecular Function Annotations

genes performing the potassium channel regulator activity molecular function from the curated GO Molecular Function Annotations dataset.

Potassium channel tetramerisation-type BTB domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel tetramerisation-type BTB domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage gated sodium channel, alpha-8 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage gated sodium channel, alpha-8 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, T-type, alpha-1 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, T-type, alpha-1 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride channel, voltage gated Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride channel, voltage gated protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage-dependent, beta subunit, KCNAB Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage-dependent, beta subunit, KCNAB protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cation channel sperm-associated protein subunit beta Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cation channel sperm-associated protein subunit beta protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, L-type, alpha-1C subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, L-type, alpha-1C subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage-dependent, ERG Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage-dependent, ERG protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Guanylate kinase/L-type calcium channel beta subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Guanylate kinase/L-type calcium channel beta subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium voltage-gated channel subfamily H member 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium voltage-gated channel subfamily H member 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium voltage-gated channel subfamily H member 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium voltage-gated channel subfamily H member 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium voltage-gated channel subfamily H member 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium voltage-gated channel subfamily H member 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride intracellular channel protein 4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride intracellular channel protein 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, inwardly rectifying, Kir2.1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, inwardly rectifying, Kir2.1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Two pore domain potassium channel, TWIK-1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Two pore domain potassium channel, TWIK-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Two pore domain potassium channel, TWIK-2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Two pore domain potassium channel, TWIK-2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transient receptor potential cation channel subfamily V member 5/6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transient receptor potential cation channel subfamily V member 5/6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage gated sodium channel, alpha-5 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage gated sodium channel, alpha-5 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, T-type, alpha-1I subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, T-type, alpha-1I subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Neurotransmitter-gated ion-channel Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Neurotransmitter-gated ion-channel protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage gated sodium channel, alpha-7 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage gated sodium channel, alpha-7 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cation channel sperm-associated protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cation channel sperm-associated protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cation channel sperm-associated protein 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cation channel sperm-associated protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cation channel sperm-associated protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cation channel sperm-associated protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cation channel sperm-associated protein 4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cation channel sperm-associated protein 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, N-type, alpha-1 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, N-type, alpha-1 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transient receptor potential channel, vanilloid 1-4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transient receptor potential channel, vanilloid 1-4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent anion-selective channel protein 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent anion-selective channel protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent anion-selective channel protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent anion-selective channel protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent anion-selective channel protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent anion-selective channel protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, Kv3, inactivation domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, Kv3, inactivation domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, R-type, alpha-1 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, R-type, alpha-1 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ion channel regulatory protein, UNC-93 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ion channel regulatory protein, UNC-93 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, gamma-1 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, gamma-1 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, gamma subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, gamma subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, inwardly rectifying, Kir, cytoplasmic Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, inwardly rectifying, Kir, cytoplasmic protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Two pore domain potassium channel, THIK Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Two pore domain potassium channel, THIK protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Na+ channel, amiloride-sensitive, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Na+ channel, amiloride-sensitive, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage-dependent, EAG Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage-dependent, EAG protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, Kv1.4, tandem inactivation domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, Kv1.4, tandem inactivation domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Neurotransmitter-gated ion-channel, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Neurotransmitter-gated ion-channel, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage gated sodium channel, alpha subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage gated sodium channel, alpha subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, Kv1.6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, Kv1.6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, Kv1.4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, Kv1.4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, Kv1.5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, Kv1.5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, Kv1.2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, Kv1.2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, Kv1.3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, Kv1.3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, Kv1.1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, Kv1.1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cation channel sperm-associated protein, subunit gamma Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cation channel sperm-associated protein, subunit gamma protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, gamma-7 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, gamma-7 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel subfamily K member 15 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel subfamily K member 15 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transient receptor ion channel domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transient receptor ion channel domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel,T-type, alpha-1G subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel,T-type, alpha-1G subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, Kv2.1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, Kv2.1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, Kv2.2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, Kv2.2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, inwardly rectifying, Kir Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, inwardly rectifying, Kir protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage gated sodium channel, alpha-4 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage gated sodium channel, alpha-4 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage gated sodium channel, alpha-4 subunit, mammalian Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage gated sodium channel, alpha-4 subunit, mammalian protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage-dependent, beta subunit, KCNE Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage-dependent, beta subunit, KCNE protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transient receptor potential ankyrin 1 channel Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transient receptor potential ankyrin 1 channel protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage-dependent, beta subunit, KCNAB1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage-dependent, beta subunit, KCNAB1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage-dependent, beta subunit, KCNAB3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage-dependent, beta subunit, KCNAB3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage-dependent, beta subunit, KCNAB2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage-dependent, beta subunit, KCNAB2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, gamma-5 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, gamma-5 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, gamma-6 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, gamma-6 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, inwardly rectifying, Kir1.3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, inwardly rectifying, Kir1.3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, inwardly rectifying, Kir1.2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, inwardly rectifying, Kir1.2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, inwardly rectifying, Kir1.1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, inwardly rectifying, Kir1.1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, calcium-activated, BK, beta subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, calcium-activated, BK, beta subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Na+ channel, amiloride-sensitive Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Na+ channel, amiloride-sensitive protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, KCNQ Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, KCNQ protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, inwardly rectifying, Kir5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, inwardly rectifying, Kir5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, gamma-2 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, gamma-2 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Sodium channel subunit beta-1/beta-3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Sodium channel subunit beta-1/beta-3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, inwardly rectifying, Kir, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, inwardly rectifying, Kir, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Calcium release-activated calcium channel protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Calcium release-activated calcium channel protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage gated sodium channel, alpha-11 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage gated sodium channel, alpha-11 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Two pore domain potassium channel Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Two pore domain potassium channel protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Neurotransmitter-gated ion-channel transmembrane domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Neurotransmitter-gated ion-channel transmembrane domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Inward rectifier potassium channel 13 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Inward rectifier potassium channel 13 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Sodium channel subunit beta-2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Sodium channel subunit beta-2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, alpha-1 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, alpha-1 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel gamma-like subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel gamma-like subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Epithelial sodium channel Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Epithelial sodium channel protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, Kv4, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, Kv4, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, inwardly rectifying, Kir6.1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, inwardly rectifying, Kir6.1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, inwardly rectifying, Kir6.2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, inwardly rectifying, Kir6.2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Intracellular chloride channel Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Intracellular chloride channel protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Two pore domain potassium channel domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Two pore domain potassium channel domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, Kv Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, Kv protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, Kv3.4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, Kv3.4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, Kv3.1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, Kv3.1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, Kv3.3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, Kv3.3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage gated sodium channel, alpha-3 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage gated sodium channel, alpha-3 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, L-type, alpha-1F subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, L-type, alpha-1F subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, L-type, alpha-1D subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, L-type, alpha-1D subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Two pore domain potassium channel, TRAAK Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Two pore domain potassium channel, TRAAK protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage gated sodium channel, alpha-10 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage gated sodium channel, alpha-10 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Two pore domain potassium channel, TASK family Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Two pore domain potassium channel, TASK family protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, gamma-4 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, gamma-4 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, inwardly rectifying, Kir2.2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, inwardly rectifying, Kir2.2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, inwardly rectifying, Kir2.3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, inwardly rectifying, Kir2.3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent channel, four helix bundle domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent channel, four helix bundle domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel subfamily K member 9 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel subfamily K member 9 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel subfamily K member 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel subfamily K member 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Polycystin cation channel Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Polycystin cation channel protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Neurotransmitter-gated ion-channel ligand-binding domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Neurotransmitter-gated ion-channel ligand-binding domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transient receptor potential channel, canonical 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transient receptor potential channel, canonical 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transient receptor potential channel, canonical 4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transient receptor potential channel, canonical 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transient receptor potential channel, canonical 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transient receptor potential channel, canonical 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transient receptor potential channel, canonical 6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transient receptor potential channel, canonical 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transient receptor potential channel, canonical 7 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transient receptor potential channel, canonical 7 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, P/Q-type, alpha-1 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, P/Q-type, alpha-1 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Calcium channel flower Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Calcium channel flower protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, Kv4.3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, Kv4.3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, Kv4.2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, Kv4.2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, Kv4.1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, Kv4.1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride channel, core Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride channel, core protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Sodium channel subunit beta-3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Sodium channel subunit beta-3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, L-type, alpha-1 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, L-type, alpha-1 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, KCNQ, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, KCNQ, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transient receptor potential channel Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transient receptor potential channel protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, L-type, beta-1 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, L-type, beta-1 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, inwardly rectifying, Kir3.1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, inwardly rectifying, Kir3.1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, inwardly rectifying, Kir3.3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, inwardly rectifying, Kir3.3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, inwardly rectifying, Kir3.2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, inwardly rectifying, Kir3.2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, inwardly rectifying, Kir3.4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, inwardly rectifying, Kir3.4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

TVP18/Calcium channel flower Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the TVP18/Calcium channel flower protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage-dependent, beta subunit, KCNAB-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage-dependent, beta subunit, KCNAB-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Kv channel-interacting protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Kv channel-interacting protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, L-type, beta subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, L-type, beta subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

TRIC channel Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the TRIC channel protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, calcium-activated, SK Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, calcium-activated, SK protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-gated potassium channel Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-gated potassium channel protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transient receptor potential channel, vanilloid 6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transient receptor potential channel, vanilloid 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, L-type, beta-3 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, L-type, beta-3 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, alpha-2/delta subunit, conserved region Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, alpha-2/delta subunit, conserved region protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, L-type, beta-2 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, L-type, beta-2 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, T-type, alpha-1H subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, T-type, alpha-1H subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage-dependent, EAG/ELK/ERG Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage-dependent, EAG/ELK/ERG protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Sodium leak channel non-selective protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Sodium leak channel non-selective protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Two pore domain potassium channel, TREK Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Two pore domain potassium channel, TREK protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, KCNQ4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, KCNQ4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, KCNQ3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, KCNQ3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, KCNQ2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, KCNQ2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, KCNQ1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, KCNQ1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Polycystin cation channel, PKD1/PKD2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Polycystin cation channel, PKD1/PKD2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transient receptor potential channel, canonical 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transient receptor potential channel, canonical 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, plant-type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, plant-type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transient receptor potential cation channel subfamily M member 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transient receptor potential cation channel subfamily M member 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transient receptor potential cation channel subfamily M member 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transient receptor potential cation channel subfamily M member 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transient receptor potential cation channel subfamily M member 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transient receptor potential cation channel subfamily M member 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transient receptor potential cation channel subfamily M member 6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transient receptor potential cation channel subfamily M member 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transient receptor potential cation channel subfamily M member 7 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transient receptor potential cation channel subfamily M member 7 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transient receptor potential cation channel subfamily M member 4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transient receptor potential cation channel subfamily M member 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transient receptor potential cation channel subfamily M member 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transient receptor potential cation channel subfamily M member 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transient receptor potential cation channel subfamily M member 8 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transient receptor potential cation channel subfamily M member 8 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride channel ClC-K Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride channel ClC-K protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride channel ClC-4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride channel ClC-4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride channel ClC-5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride channel ClC-5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride channel ClC-6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride channel ClC-6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride channel ClC-7 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride channel ClC-7 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride channel ClC-1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride channel ClC-1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride channel ClC-2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride channel ClC-2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride channel ClC-3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride channel ClC-3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage gated sodium channel, alpha-1 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage gated sodium channel, alpha-1 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride intracellular channel protein 6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride intracellular channel protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride intracellular channel protein 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride intracellular channel protein 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride intracellular channel protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride intracellular channel protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride intracellular channel protein 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride intracellular channel protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride intracellular channel protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride intracellular channel protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, L-type, alpha-1S subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, L-type, alpha-1S subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, Kv8.1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, Kv8.1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transient receptor potential cation channel subfamily V member 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transient receptor potential cation channel subfamily V member 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, alpha-1 subunit, IQ domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, alpha-1 subunit, IQ domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Cation channel sperm-associated protein subunit delta Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Cation channel sperm-associated protein subunit delta protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride channel calcium-activated Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride channel calcium-activated protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Two pore domain potassium channel, TWIK family Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Two pore domain potassium channel, TWIK family protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage gated sodium channel, alpha-9 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage gated sodium channel, alpha-9 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transient receptor potential channel, vanilloid 4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transient receptor potential channel, vanilloid 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transient receptor potential channel, vanilloid 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transient receptor potential channel, vanilloid 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transient receptor potential channel, vanilloid 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transient receptor potential channel, vanilloid 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transient receptor potential channel, vanilloid 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transient receptor potential channel, vanilloid 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Two pore calcium channel protein 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Two pore calcium channel protein 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Two pore calcium channel protein 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Two pore calcium channel protein 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage-dependent, beta subunit, KCNE2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage-dependent, beta subunit, KCNE2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage-dependent, beta subunit, KCNE3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage-dependent, beta subunit, KCNE3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage-dependent, beta subunit, KCNE1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage-dependent, beta subunit, KCNE1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, calcium-activated, BK, alpha subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, calcium-activated, BK, alpha subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Transient receptor potential channel, canonical Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Transient receptor potential channel, canonical protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Voltage-dependent calcium channel, gamma-8 subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Voltage-dependent calcium channel, gamma-8 subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Calcium-activated chloride channel protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Calcium-activated chloride channel protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Chloride channel CLIC-like Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Chloride channel CLIC-like protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage-dependent, ELK Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage-dependent, ELK protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, Kv3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, Kv3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, Kv2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, Kv2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, Kv1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, Kv1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, Kv6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, Kv6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, Kv4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, Kv4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Potassium channel, voltage dependent, Kv9 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Potassium channel, voltage dependent, Kv9 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal channel response Gene Set

From MPO Gene-Phenotype Associations

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

decreased channel response intensity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased channel response intensity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased channel response threshold Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased channel response threshold phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal channel response intensity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal channel response intensity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal channel response threshold Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal channel response threshold phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

channel Gene Set

From Phosphosite Textmining Biological Term Annotations

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

ion-channel-gating Gene Set

From Phosphosite Textmining Biological Term Annotations

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

TWIK-related spinal cord K+ channel (TRESK) Gene Set

From Reactome Pathways

proteins participating in the TWIK-related spinal cord K+ channel (TRESK) pathway from the Reactome Pathways dataset.

TWIK-related alkaline pH activated K+ channel (TALK) Gene Set

From Reactome Pathways

proteins participating in the TWIK-related alkaline pH activated K+ channel (TALK) pathway from the Reactome Pathways dataset.

Ligand-gated ion channel transport Gene Set

From Reactome Pathways

proteins participating in the Ligand-gated ion channel transport pathway from the Reactome Pathways dataset.

Ion channel transport Gene Set

From Reactome Pathways

proteins participating in the Ion channel transport pathway from the Reactome Pathways dataset.

TWIK-releated acid-sensitive K+ channel (TASK) Gene Set

From Reactome Pathways

proteins participating in the TWIK-releated acid-sensitive K+ channel (TASK) pathway from the Reactome Pathways dataset.

TWIK related potassium channel (TREK) Gene Set

From Reactome Pathways

proteins participating in the TWIK related potassium channel (TREK) pathway from the Reactome Pathways dataset.

Tandem pore domain halothane-inhibited K+ channel (THIK) Gene Set

From Reactome Pathways

proteins participating in the Tandem pore domain halothane-inhibited K+ channel (THIK) pathway from the Reactome Pathways dataset.

Lynch syndrome:Turcot syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Hereditary cancer-predisposing syndrome:Lynch syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Zunich neuroectodermal syndrome:Zunich neuroectodermal syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Von Hippel-Lindau syndrome:Hereditary cancer-predisposing syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Von Hippel-Lindau syndrome:Hereditary cancer-predisposing syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Noonan syndrome and Noonan-related syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Lynch syndrome:Hereditary cancer-predisposing syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Lynch syndrome:Lynch syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Marfan's syndrome:Marfan's syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Hereditary cancer-predisposing syndrome:Peutz-Jeghers syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hereditary cancer-predisposing syndrome:Peutz-Jeghers syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

IFAP syndrome with or without BRESHECK syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the IFAP syndrome with or without BRESHECK syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lynch syndrome I:Lynch syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Hereditary cancer-predisposing syndrome:Hereditary cancer-predisposing syndrome Gene Set

From ClinVar Gene-Phenotype Associations

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

Miller-McKusick-Malvaux-Syndrome (3M Syndrome) Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Miller-McKusick-Malvaux-Syndrome (3M Syndrome) from the curated CTD Gene-Disease Associations dataset.

Digeorge Syndrome/Velocardiofacial Syndrome Complex 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Digeorge Syndrome/Velocardiofacial Syndrome Complex 2 from the curated CTD Gene-Disease Associations dataset.

menarch; natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious Gene Set

From GAD Gene-Disease Associations

genes associated with the disease menarch; natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amyloidosis; behcet syndrome; familial mediterranean fever; irritable bowel syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; cystic fibrosis; klinefelter syndrome; klinefelter's syndrome; oligospermia; sex chromosome aberrations; translocation, genetic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

hyperhomocysteinemia; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

cornelia de lange syndrome; de lange syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cornelia de lange syndrome; de lange syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fatigue syndrome, chronic; fatigue syndrome; postviral Gene Set

From GAD Gene-Disease Associations

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

pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, multiple; aortic aneurysm, thoracic; marfan syndrome; syndrome Gene Set

From GAD Gene-Disease Associations

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

resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene Set

From GAD Gene-Disease Associations

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

obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obstetric labor, premature; resp distress syndrome neonatal; respiratory distress syndrome, newborn; tachycardia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hyperandrogenism; polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bronchopulmonary dysplasia; resp distress syndrome neonatal; respiratory distress syndrome, newborn; respiratory tract infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lung diseases; resp distress syndrome neonatal; respiratory distress syndrome, newborn Gene Set

From GAD Gene-Disease Associations

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

hyperandrogenism; insulin resistance; obesity; polycystic ovarian syndrome; polycystic ovary syndrome; thinness Gene Set

From GAD Gene-Disease Associations

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

restless legs syndrome; tourette syndrome Gene Set

From GAD Gene-Disease Associations

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

endometriosis; infertility, female; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease endometriosis; infertility, female; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

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

obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; natural menopause; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal alcohol syndrome; syndrome; fetal, alcohol (dysmorphic) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal alcohol syndrome; syndrome; fetal, alcohol (dysmorphic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

behcet syndrome; uveomeningoencephalitic syndrome Gene Set

From GAD Gene-Disease Associations

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

hyperandrogenism; hyperinsulinism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

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

autoimmune thyroiditis; helicobacter infections; thyroiditis, autoimmune; turner syndrome; xo syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune thyroiditis; helicobacter infections; thyroiditis, autoimmune; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infertility, female; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

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

autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease autoimmune diseases; chromosome aberrations; chromosome abnormality; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

melas syndrome; merrf syndrome Gene Set

From GAD Gene-Disease Associations

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

haemolytic-uraemic syndrome; hemolytic-uremic syndrome; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease haemolytic-uraemic syndrome; hemolytic-uremic syndrome; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease natural menopause; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious; thrombophilia; tobacco use disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

infertility; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

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

abnormalities, multiple; genetic diseases, inborn; kallmann syndrome; syndrome Gene Set

From GAD Gene-Disease Associations

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

angelman syndrome; rett syndrome; seizures Gene Set

From GAD Gene-Disease Associations

genes associated with the disease angelman syndrome; rett syndrome; seizures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis; carpal tunnel syndrome; cryoglobulinemia; hepatitis c, chronic; sjogren's syndrome; thyroiditis, autoimmune Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis; carpal tunnel syndrome; cryoglobulinemia; hepatitis c, chronic; sjogren's syndrome; thyroiditis, autoimmune in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose intolerance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

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

escherichia coli infections; haemolytic-uraemic syndrome; hemolytic-uremic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease escherichia coli infections; haemolytic-uraemic syndrome; hemolytic-uremic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

digeorge syndrome; memory disorders; pharyngeal pouch; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease digeorge syndrome; memory disorders; pharyngeal pouch; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult respiratory distress syndrome; chromosome deletion; respiratory distress syndrome, adult Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; noonan syndrome; pulmonary valve stenosis; syndrome; turner's phenotype, karyotype normal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiomyopathy, hypertrophic; hypertrophic cardiomyopathy; noonan syndrome; pulmonary valve stenosis; syndrome; turner's phenotype, karyotype normal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic renal failure; haemolytic-uraemic syndrome; hemolytic-uremic syndrome; kidney failure, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic renal failure; haemolytic-uraemic syndrome; hemolytic-uremic syndrome; kidney failure, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

metabolic syndrome ; metabolic syndrome Gene Set

From GAD Gene-Disease Associations

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

obesity; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

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

digeorge syndrome; pharyngeal pouch; syndrome Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

haemolytic-uraemic syndrome; hemolytic-uremic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease haemolytic-uraemic syndrome; hemolytic-uremic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

inflammation; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

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

birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; fetal alcohol syndrome; fetal growth retardation; intrauterine growth retardation; syndrome; fetal, alcohol (dysmorphic) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antithrombin iii deficiency; gastrointestinal hemorrhage; protein c deficiency; protein s deficiency; splenomegaly; thrombophilia; turner syndrome; venous thrombosis; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic ovarian syndrome; polycystic ovary syndrome; puberty, precocious Gene Set

From GAD Gene-Disease Associations

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

carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carbohydrate metabolism, inborn errors; dyskinesias; dyskinetic syndrome; epilepsy; mental retardation; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; klinefelter syndrome; klinefelter's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brugada syndrome; chromosome deletion; death, sudden, cardiac; long qt syndrome; sudden cardiac death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hantavirus infections; hantavirus pulmonary syndrome; heart diseases; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hantavirus infections; hantavirus pulmonary syndrome; heart diseases; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenomatous polyposis coli; bone neoplasms; epidermal cyst; gardner syndrome; gardner's syndrome; osteoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenomatous polyposis coli; bone neoplasms; epidermal cyst; gardner syndrome; gardner's syndrome; osteoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute lung injury; adult respiratory distress syndrome; respiratory distress syndrome, adult; sepsis; systemic infection Gene Set

From GAD Gene-Disease Associations

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

down syndrome; ehlers-danlos syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease down syndrome; ehlers-danlos syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis; felty's syndrome; large granular lymphocyte syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis; felty's syndrome; large granular lymphocyte syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

polycystic ovarian syndrome; polycystic ovary syndrome; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

menarch; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious Gene Set

From GAD Gene-Disease Associations

genes associated with the disease menarch; obesity; pof - premature ovarian failure; polycystic ovarian syndrome; polycystic ovary syndrome; primary ovarian insufficiency; puberty, delayed; puberty, precocious in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heart-hand syndrome, holt-oram syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart-hand syndrome, holt-oram syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gynecomastia; klinefelter syndrome; klinefelter's syndrome; oligospermia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gynecomastia; klinefelter syndrome; klinefelter's syndrome; oligospermia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adult respiratory distress syndrome; community-acquired infections; pneumonia; respiratory distress syndrome, adult; septic shock; shock, septic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adult respiratory distress syndrome; community-acquired infections; pneumonia; respiratory distress syndrome, adult; septic shock; shock, septic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aneurysm, dissecting; aortic aneurysm, thoracic; loeys-dietz syndrome; marfan syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aneurysm, dissecting; aortic aneurysm, thoracic; loeys-dietz syndrome; marfan syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; glucose intolerance; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

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

hirsutism; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

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

haemolytic-uraemic syndrome; hematologic diseases; hemolytic-uremic syndrome; purpura, thrombocytopenic; thrombocytopenic purpura Gene Set

From GAD Gene-Disease Associations

genes associated with the disease haemolytic-uraemic syndrome; hematologic diseases; hemolytic-uremic syndrome; purpura, thrombocytopenic; thrombocytopenic purpura in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dwarfism, pituitary; pituitary dwarfism; turner syndrome; xo syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dwarfism, pituitary; pituitary dwarfism; turner syndrome; xo syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

stuve-wiedemann syndrome/schwartz-jampel type 2 syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the stuve-wiedemann syndrome/schwartz-jampel type 2 syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

digeorge syndrome/velocardiofacial syndrome complex-2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the digeorge syndrome/velocardiofacial syndrome complex-2 phenotype from the curated OMIM Gene-Disease Associations dataset.

ifap syndrome with or without bresheck syndrome Gene Set

From OMIM Gene-Disease Associations

genes associated with the ifap syndrome with or without bresheck syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.

Congenital myotonia, autosomal dominant form Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital myotonia, autosomal dominant form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital adrenal hyperplasia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital adrenal hyperplasia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital human immunodeficiency virus Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital human immunodeficiency virus phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-ige 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.

Diarrhea 5, with tufting enteropathy, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diarrhea 5, with tufting enteropathy, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Vertical talus, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Vertical talus, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital generalized lipodystrophy type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital generalized lipodystrophy type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glycogen storage disease IV, congenital neuromuscular Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glycogen storage disease IV, congenital neuromuscular phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leber congenital amaurosis 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leber congenital amaurosis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leber congenital amaurosis 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leber congenital amaurosis 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Facial paresis, hereditary congenital, 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Facial paresis, hereditary congenital, 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leber congenital amaurosis 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leber congenital amaurosis 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leber congenital amaurosis 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leber congenital amaurosis 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leber congenital amaurosis 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leber congenital amaurosis 9 phenotype from the curated ClinVar Gene-Phenotype 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.

Congenital sensory neuropathy with selective loss of small myelinated fibers Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital sensory neuropathy with selective loss of small myelinated fibers phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, actin, congenital, with cores Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, actin, congenital, with cores phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Aphakia, congenital primary Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Aphakia, congenital primary phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Lipodystrophy, congenital generalized, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Lipodystrophy, congenital generalized, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital contractural arachnodactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital contractural arachnodactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leber congenital amaurosis 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leber congenital amaurosis 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe congenital neutropenia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe congenital neutropenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital absence of salivary gland Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital absence of salivary gland phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Merosin deficient congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Merosin deficient congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nystagmus 6, congenital, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nystagmus 6, congenital, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, autosomal dominant 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, autosomal dominant 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Afibrinogenemia, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Afibrinogenemia, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, congenital heart defects, and posterior embryotoxon Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, congenital heart defects, and posterior embryotoxon phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

Adrenal insufficiency, congenital, with 46,XY sex reversal, partial or complete Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adrenal insufficiency, congenital, with 46,XY sex reversal, partial or complete phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Walker-Warburg congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Walker-Warburg congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fibrosis of extraocular muscles, congenital, 3b Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fibrosis of extraocular muscles, congenital, 3b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital amegakaryocytic thrombocytopenia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital amegakaryocytic thrombocytopenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, autosomal recessive congenital 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, autosomal recessive congenital 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Diarrhea 3, secretory sodium, congenital, syndromic Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Diarrhea 3, secretory sodium, congenital, syndromic phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe congenital neutropenia 3, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe congenital neutropenia 3, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital dyserythropoietic anemia, type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital dyserythropoietic anemia, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital adrenal hypoplasia, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital adrenal hypoplasia, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital secretory diarrhea, chloride type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital secretory diarrhea, chloride type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypomyelination and Congenital Cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypomyelination and Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fibrosis of extraocular muscles, congenital, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fibrosis of extraocular muscles, congenital, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fibrosis of extraocular muscles, congenital, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fibrosis of extraocular muscles, congenital, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Testicular anomalies with or without congenital heart disease Gene Set

From ClinVar Gene-Phenotype Associations

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

LIPOPROTEIN(a) DEFICIENCY, CONGENITAL Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the LIPOPROTEIN(a) DEFICIENCY, CONGENITAL phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 1, X-LINKED phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

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

From ClinVar Gene-Phenotype Associations

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

Congenital heart disease, multiple types, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital heart disease, multiple types, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIm phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe congenital neutropenia X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe congenital neutropenia X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Indifference to pain, congenital, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Indifference to pain, congenital, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, autosomal dominant 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, autosomal dominant 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fibrosis of extraocular muscles, congenital, 3a, with or without extraocular involvement phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital heart defects, multiple types, 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital heart defects, multiple types, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital erythropoietic porphyria Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital erythropoietic porphyria phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

congenital neutropenia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the congenital neutropenia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypothyroidism, congenital, nongoitrous, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypothyroidism, congenital, nongoitrous, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypothyroidism, congenital, nongoitrous, 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypothyroidism, congenital, nongoitrous, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypothyroidism, congenital, nongoitrous, 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypothyroidism, congenital, nongoitrous, 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1s Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1s phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1L Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, actin, congenital, with excess of thin myofilaments Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, actin, congenital, with excess of thin myofilaments phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive congenital ichthyosis 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive congenital ichthyosis 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Eichsfeld type congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Eichsfeld type congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 2B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 2C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 2C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 2J Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 2J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 2L Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 2L phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iw phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Congenital disorder of glycosylation type 2k Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 2k phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, congenital, with excess of muscle spindles Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, congenital, with excess of muscle spindles phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy without mental retardation, type B5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital lactase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital lactase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital myotonia, autosomal recessive form Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital myotonia, autosomal recessive form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe congenital neutropenia 6, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe congenital neutropenia 6, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1Q Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1Q phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1P Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1P phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

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

From ClinVar Gene-Phenotype Associations

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

Congenital disorder of glycosylation type 1H Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1H phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1N Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1N phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bile acid synthesis defect, congenital, 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bile acid synthesis defect, congenital, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bile acid synthesis defect, congenital, 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bile acid synthesis defect, congenital, 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1v Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1v phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, congenital nuclear, autosomal recessive 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, congenital nuclear, autosomal recessive 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, congenital nuclear, autosomal recessive 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, congenital nuclear, autosomal recessive 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spondyloepiphyseal dysplasia with congenital joint dislocations Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spondyloepiphyseal dysplasia with congenital joint dislocations phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Muscular dystrophy, congenital, due to ITGA7 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Muscular dystrophy, congenital, due to ITGA7 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Adult i Blood Group with or without Congenital Cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adult i Blood Group with or without Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, congenital, compton-north Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, congenital, compton-north phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

T-cell immunodeficiency, congenital alopecia and nail dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the T-cell immunodeficiency, congenital alopecia and nail dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital cystic disease of liver Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital cystic disease of liver phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pancreatic agenesis and congenital heart disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pancreatic agenesis and congenital heart disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type Ix Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type Ix phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital order of glycosylation type 1r Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital order of glycosylation type 1r phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ullrich congenital muscular dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ullrich congenital muscular dystrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leber congenital amaurosis 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leber congenital amaurosis 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital dyserythropoietic anemia, type II Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital dyserythropoietic anemia, type II phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neuropathy, congenital hypomyelinating, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neuropathy, congenital hypomyelinating, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 2B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 2A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital central hypoventilation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital central hypoventilation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe congenital neutropenia autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe congenital neutropenia autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital ocular coloboma Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital ocular coloboma phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1K Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1K phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1J Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1J phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1O Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1O phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1D Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1D phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1G Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1G phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1y Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1y phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Digital clubbing, isolated congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Digital clubbing, isolated congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1u Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1u phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital disorder of glycosylation type 1t Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital disorder of glycosylation type 1t phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anti-plasmin deficiency, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Anti-plasmin deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Prothrombin deficiency, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Prothrombin deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe congenital neutropenia 2, autosomal dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe congenital neutropenia 2, autosomal dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital defect of folate absorption Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital defect of folate absorption phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Severe congenital neutropenia 4, autosomal recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Severe congenital neutropenia 4, autosomal recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital aniridia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital aniridia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital hyperammonemia, type I Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital hyperammonemia, type I phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy due to partial LAMA2 deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy due to partial LAMA2 deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Multiple congenital exostosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Multiple congenital exostosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital muscular dystrophy-dystroglycanopathy with mental retardation, type B3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive congenital ichthyosis 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive congenital ichthyosis 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive congenital ichthyosis 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive congenital ichthyosis 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive congenital ichthyosis 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive congenital ichthyosis 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive congenital ichthyosis 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive congenital ichthyosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive congenital ichthyosis 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive congenital ichthyosis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glutamine deficiency, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glutamine deficiency, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leber congenital amaurosis 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leber congenital amaurosis 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital microvillous atrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital microvillous atrophy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leber congenital amaurosis 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leber congenital amaurosis 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leber congenital amaurosis 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leber congenital amaurosis 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leber congenital amaurosis 15 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leber congenital amaurosis 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Leber congenital amaurosis 17 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Leber congenital amaurosis 17 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Partial congenital absence of teeth Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Partial congenital absence of teeth phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 1C Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 1C phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 1B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 1A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 1F Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 1F phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital stationary night blindness, type 1E Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital stationary night blindness, type 1E phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive congenital ichthyosis 4A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive congenital ichthyosis 4A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Autosomal recessive congenital ichthyosis 4B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Autosomal recessive congenital ichthyosis 4B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the ANEMIA, CONGENITAL DYSERYTHROPOIETIC, TYPE Ib phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glaucoma, congenital Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glaucoma, congenital phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital Cataracts, Facial Dysmorphism, and Neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital Cataracts, Facial Dysmorphism, and Neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital Stromal Corneal Dystrophy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital Stromal Corneal Dystrophy 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.

Congenital myopathy with fiber type disproportion Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital myopathy with fiber type disproportion phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital Hyperinsulinism Gene Set

From CTD Gene-Disease Associations

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

Cataract congenital Volkmann type Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract congenital Volkmann type from the curated CTD Gene-Disease Associations dataset.

Congenital adrenal hyperplasia due to 21 hydroxylase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital adrenal hyperplasia due to 21 hydroxylase deficiency from the curated CTD Gene-Disease Associations dataset.

Congenital Hypothyroidism Gene Set

From CTD Gene-Disease Associations

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

Congenital bilateral aplasia of vas deferens Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital bilateral aplasia of vas deferens from the curated CTD Gene-Disease Associations dataset.

Congenital Abnormalities Gene Set

From CTD Gene-Disease Associations

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

Anemia, Hemolytic, Congenital Nonspherocytic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Hemolytic, Congenital Nonspherocytic from the curated CTD Gene-Disease Associations dataset.

Night Blindness, Congenital Stationary, Autosomal Dominant 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Night Blindness, Congenital Stationary, Autosomal Dominant 3 from the curated CTD Gene-Disease Associations dataset.

Hypothyroidism, Congenital, Nongoitrous, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypothyroidism, Congenital, Nongoitrous, 4 from the curated CTD Gene-Disease Associations dataset.

Leber Congenital Amaurosis 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leber Congenital Amaurosis 4 from the curated CTD Gene-Disease Associations dataset.

Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, Congenital, with Inner Ear Agenesis, Microtia, and Microdontia from the curated CTD Gene-Disease Associations dataset.

Congenital idiopathic intestinal pseudoobstruction Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital idiopathic intestinal pseudoobstruction from the curated CTD Gene-Disease Associations dataset.

Vertical talus, congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Vertical talus, congenital from the curated CTD Gene-Disease Associations dataset.

Nystagmus 1, congenital, X- linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nystagmus 1, congenital, X- linked from the curated CTD Gene-Disease Associations dataset.

Facial paresis, hereditary, congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Facial paresis, hereditary, congenital from the curated CTD Gene-Disease Associations dataset.

Congenital anosmia Gene Set

From CTD Gene-Disease Associations

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

Hypothyroidism, Congenital, Nongoitrous, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypothyroidism, Congenital, Nongoitrous, 5 from the curated CTD Gene-Disease Associations dataset.

Hyperferritinemia, hereditary, with congenital cataracts Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hyperferritinemia, hereditary, with congenital cataracts from the curated CTD Gene-Disease Associations dataset.

Ichthyosiform erythroderma, Brocq congenital, nonbullous form Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ichthyosiform erythroderma, Brocq congenital, nonbullous form from the curated CTD Gene-Disease Associations dataset.

Neutropenia, Severe Congenital, Autosomal Dominant 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neutropenia, Severe Congenital, Autosomal Dominant 2 from the curated CTD Gene-Disease Associations dataset.

Hernias, Diaphragmatic, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hernias, Diaphragmatic, Congenital from the curated CTD Gene-Disease Associations dataset.

Congenital Disorder Of Glycosylation, Type IIF Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type IIF from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1A from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation, type 2C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation, type 2C from the curated CTD Gene-Disease Associations dataset.

Aphakia, congenital primary Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Aphakia, congenital primary 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.

Congenital thrombotic disease, due to Protein C deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital thrombotic disease, due to Protein C deficiency from the curated CTD Gene-Disease Associations dataset.

Nystagmus 2, congenital, autosomal dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nystagmus 2, congenital, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

Hypothyroidism, Congenital, Nongoitrous, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypothyroidism, Congenital, Nongoitrous, 3 from the curated CTD Gene-Disease Associations dataset.

Congenital contractural arachnodactyly Gene Set

From CTD Gene-Disease Associations

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

Lactase Deficiency, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lactase Deficiency, Congenital from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 2D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 2D from the curated CTD Gene-Disease Associations dataset.

Nystagmus 4, congenital, autosomal dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nystagmus 4, congenital, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects from the curated CTD Gene-Disease Associations dataset.

Anti-plasmin deficiency, congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anti-plasmin deficiency, congenital from the curated CTD Gene-Disease Associations dataset.

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iq Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iq from the curated CTD Gene-Disease Associations dataset.

Muscular dystrophy congenital, merosin negative Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular dystrophy congenital, merosin negative from the curated CTD Gene-Disease Associations dataset.

Indifference to Pain, Congenital, Autosomal Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Indifference to Pain, Congenital, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset.

Ptosis, Hereditary Congenital 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ptosis, Hereditary Congenital 1 from the curated CTD Gene-Disease Associations dataset.

Pain Insensitivity, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Pain Insensitivity, Congenital from the curated CTD Gene-Disease Associations dataset.

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIi from the curated CTD Gene-Disease Associations dataset.

MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MYOPATHY, CONGENITAL, WITH FIBER-TYPE DISPROPORTION from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1G Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1G from the curated CTD Gene-Disease Associations dataset.

Congenital amegakaryocytic thrombocytopenia Gene Set

From CTD Gene-Disease Associations

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

Adrenal Hyperplasia, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Adrenal Hyperplasia, Congenital from the curated CTD Gene-Disease Associations dataset.

NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2B from the curated CTD Gene-Disease Associations dataset.

Anemia, Hypoplastic, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Hypoplastic, Congenital from the curated CTD Gene-Disease Associations dataset.

Congenital Cataracts, Facial Dysmorphism, And Neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Cataracts, Facial Dysmorphism, And Neuropathy from the curated CTD Gene-Disease Associations dataset.

Lipodystrophy, Congenital Generalized Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lipodystrophy, Congenital Generalized from the curated CTD Gene-Disease Associations dataset.

Congenital hypertrichosis lanuginosa Gene Set

From CTD Gene-Disease Associations

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

Leber Congenital Amaurosis 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leber Congenital Amaurosis 10 from the curated CTD Gene-Disease Associations dataset.

Hypothyroidism, Congenital, Nongoitrous, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypothyroidism, Congenital, Nongoitrous, 2 from the curated CTD Gene-Disease Associations dataset.

Myopathy, Congenital, Compton-North Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Congenital, Compton-North from the curated CTD Gene-Disease Associations dataset.

Leber Congenital Amaurosis 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leber Congenital Amaurosis 3 from the curated CTD Gene-Disease Associations dataset.

Congenital Disorder of Glycosylation, Type Io Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Disorder of Glycosylation, Type Io from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, Due To Integrin Alpha-7 Deficiency from the curated CTD Gene-Disease Associations dataset.

Congenital Disorder Of Glycosylation, Type Im Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type Im from the curated CTD Gene-Disease Associations dataset.

Congenital Disorder Of Glycosylation, Type In Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital Disorder Of Glycosylation, Type In from the curated CTD Gene-Disease Associations dataset.

Cataract, Congenital Zonular, with Sutural Opacities Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Congenital Zonular, with Sutural Opacities from the curated CTD Gene-Disease Associations dataset.

Microcoria, congenital Gene Set

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

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

From CTD Gene-Disease Associations

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

Anemia, Hemolytic, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Hemolytic, Congenital from the curated CTD Gene-Disease Associations dataset.

Bile acid synthesis defect, congenital, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bile acid synthesis defect, congenital, 2 from the curated CTD Gene-Disease Associations dataset.

Bile acid synthesis defect, congenital, 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bile acid synthesis defect, congenital, 4 from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, 1B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, 1B from the curated CTD Gene-Disease Associations dataset.

Leber Congenital Amaurosis 14 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leber Congenital Amaurosis 14 from the curated CTD Gene-Disease Associations dataset.

ADRENAL HYPOPLASIA, CONGENITAL Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ADRENAL HYPOPLASIA, CONGENITAL from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1H Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1H from the curated CTD Gene-Disease Associations dataset.

Ptosis, Hereditary Congenital 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ptosis, Hereditary Congenital 2 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 6 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 1 from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION), TYPE B, 3 from the curated CTD Gene-Disease Associations dataset.

Diarrhea 4, Malabsorptive, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Diarrhea 4, Malabsorptive, Congenital from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1J Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1J from the curated CTD Gene-Disease Associations dataset.

CAPILLARY MALFORMATIONS, CONGENITAL Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CAPILLARY MALFORMATIONS, CONGENITAL from the curated CTD Gene-Disease Associations dataset.

Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fibrosis Of Extraocular Muscles, Congenital, 3A, with or without Extraocular Involvement from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1B from the curated CTD Gene-Disease Associations dataset.

Nephrosis, congenital Gene Set

From CTD Gene-Disease Associations

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

Neutropenia, Severe Congenital, Autosomal Dominant 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neutropenia, Severe Congenital, Autosomal Dominant 1 from the curated CTD Gene-Disease Associations dataset.

GLAUCOMA 3, PRIMARY CONGENITAL, C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease GLAUCOMA 3, PRIMARY CONGENITAL, C from the curated CTD Gene-Disease Associations dataset.

Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Congenital, With Fiber-Type Disproportion, X-Linked from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 2A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 2A from the curated CTD Gene-Disease Associations dataset.

ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ARTHROGRYPOSIS, CONGENITAL, LOWER LIMB, X-LINKED from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 2E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 2E from the curated CTD Gene-Disease Associations dataset.

Muscular Dystrophy, Congenital, Merosin-Positive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Muscular Dystrophy, Congenital, Merosin-Positive from the curated CTD Gene-Disease Associations dataset.

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ip from the curated CTD Gene-Disease Associations dataset.

Myopathies, Structural, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathies, Structural, Congenital from the curated CTD Gene-Disease Associations dataset.

Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism from the curated CTD Gene-Disease Associations dataset.

ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6 from the curated CTD Gene-Disease Associations dataset.

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

From CTD Gene-Disease Associations

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

Bile acid synthesis defect, congenital, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Bile acid synthesis defect, congenital, 1 from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1F Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1F from the curated CTD Gene-Disease Associations dataset.

Cataract, Autosomal Recessive Congenital 3 Gene Set

From CTD Gene-Disease Associations

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

CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIj from the curated CTD Gene-Disease Associations dataset.

Preauricular Fistulae, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Preauricular Fistulae, Congenital from the curated CTD Gene-Disease Associations dataset.

Leber Congenital Amaurosis Gene Set

From CTD Gene-Disease Associations

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

Lower Extremity Deformities, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Lower Extremity Deformities, Congenital from the curated CTD Gene-Disease Associations dataset.

Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay from the curated CTD Gene-Disease Associations dataset.

NYSTAGMUS 5, CONGENITAL, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NYSTAGMUS 5, CONGENITAL, X-LINKED from the curated CTD Gene-Disease Associations dataset.

Night blindness, congenital stationary Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Night blindness, congenital stationary from the curated CTD Gene-Disease Associations dataset.

Fibrosis of Extraocular Muscles, Congenital, 3B Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fibrosis of Extraocular Muscles, Congenital, 3B from the curated CTD Gene-Disease Associations dataset.

Sucrase-isomaltase deficiency, congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sucrase-isomaltase deficiency, congenital from the curated CTD Gene-Disease Associations dataset.

Polycythemia, primary familial and congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polycythemia, primary familial and congenital from the curated CTD Gene-Disease Associations dataset.

Marie Unna congenital hypotrichosis Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Marie Unna congenital hypotrichosis from the curated CTD Gene-Disease Associations dataset.

NYSTAGMUS 6, CONGENITAL, X-LINKED Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NYSTAGMUS 6, CONGENITAL, X-LINKED from the curated CTD Gene-Disease Associations dataset.

Nystagmus 3, congenital, autosomal dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Nystagmus 3, congenital, autosomal dominant from the curated CTD Gene-Disease Associations dataset.

Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails from the curated CTD Gene-Disease Associations dataset.

Leber Congenital Amaurosis 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leber Congenital Amaurosis 12 from the curated CTD Gene-Disease Associations dataset.

Leber Congenital Amaurosis 13 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Leber Congenital Amaurosis 13 from the curated CTD Gene-Disease Associations dataset.

Congenital atransferrinemia Gene Set

From CTD Gene-Disease Associations

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

Congenital disorder of glycosylation type II Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type II from the curated CTD Gene-Disease Associations dataset.

Fibrosis Of Extraocular Muscles, Congenital, 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Fibrosis Of Extraocular Muscles, Congenital, 2 from the curated CTD Gene-Disease Associations dataset.

Neutropenia, Severe Congenital, X-Linked Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neutropenia, Severe Congenital, X-Linked from the curated CTD Gene-Disease Associations dataset.

ERYTHRODERMA, ICHTHYOSIFORM, CONGENITAL RETICULAR Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ERYTHRODERMA, ICHTHYOSIFORM, CONGENITAL RETICULAR from the curated CTD Gene-Disease Associations dataset.

Nystagmus, Congenital Gene Set

From CTD Gene-Disease Associations

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

Congenital disorder of glycosylation type 1K Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1K from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1L Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1L from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1C Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1C from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1E Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1E from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation type 1D Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation type 1D from the curated CTD Gene-Disease Associations dataset.

NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A from the curated CTD Gene-Disease Associations dataset.

Corneal Dystrophy, Congenital Stromal Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Corneal Dystrophy, Congenital Stromal from the curated CTD Gene-Disease Associations dataset.

MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH OR WITHOUT MENTAL RETARDATION), TYPE B, 5 from the curated CTD Gene-Disease Associations dataset.

Hand Deformities, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hand Deformities, Congenital from the curated CTD Gene-Disease Associations dataset.

PROTHROMBIN DEFICIENCY, CONGENITAL Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PROTHROMBIN DEFICIENCY, CONGENITAL from the curated CTD Gene-Disease Associations dataset.

LEBER CONGENITAL AMAUROSIS 15 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease LEBER CONGENITAL AMAUROSIS 15 from the curated CTD Gene-Disease Associations dataset.

Diarrhea 3, Secretory Sodium, Congenital Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Diarrhea 3, Secretory Sodium, Congenital from the curated CTD Gene-Disease Associations dataset.

Congenital disorder of glycosylation, type 2G Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Congenital disorder of glycosylation, type 2G from the curated CTD Gene-Disease Associations dataset.

Limb Deformities, Congenital Gene Set