Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "K"
121 to 130 of 320 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

121
Potassium voltage-gated channel subfamily D member 3
BRGDA9, KCND3L, KCND3S, KSHIVB, KV4.3, SCA19, SCA22
Atrial fibrillation, Breast cancer, Brugada syndrome, Cardiac arrhythmia, Ectopic rhythm, Hereditary ataxia, Intellectual developmental disorder, Neurodevelopmental disorders, Prostate cancer, Severe acute respiratory syndrome, Spinocerebellar ataxia, Diabetes mellitus, type 2

122
Potassium voltage-gated channel subfamily E regulatory subunit 1
ISK, JLNS, JLNS2, LQT2/5, LQT5, MinK
Arrhythmogenic right ventricular cardiomyopathy, Atrial fibrillation, Cardiomyopathy, Long qt syndrome, Hereditary atrial fibrillation, Hypertrophic cardiomyopathy, Jervell and lange-nielsen syndrome, Long qt syndrome digenic, Hearing loss

123
Potassium voltage-gated channel modifier subfamily G member 1
K13, KCNG, KV6.1, kH2
Alzheimer disease, Atypical femoral fracture, Bipolar disorder, Major depressive disorder, Schizophrenia, Diabetes mellitus, type 2

124
Potassium voltage-gated channel subfamily H member 1
EAG, EAG1, K(V)10.1, Kv10.1, TMBTS, ZLS1, h-eag, hEAG, hEAG1
Alzheimer disease, Biliary tract cancer, Breast cancer, Breast neoplasm, Cancer, Cervical cancer, Color vision deficiency, Colorectal cancer, Endometrial cancer, Epilepsy, Esophageal cancer, Estrogen-receptor negative breast cancer, Gastric cancer, Hepatocellular carcinoma, Lung cancer
View all (12 more)

125
Potassium voltage-gated channel subfamily H member 2
ERG-1, ERG1, H-ERG, HERG, HERG1, Kv11.1, LQT2, SQT1
Cardiac arrhythmias, Atrial fibrillation, Atrial flutter, Brugada syndrome, Cardiac arrhythmia, Cardioembolic stroke, Cardiomyopathy, Colonic neoplasm, Diverticular disease, Long qt syndrome, Gout, Hypertrophic cardiomyopathy, Long qt syndrome digenic, Metabolic syndrome, Non-organic psychosis
View all (8 more)

126
Potassium inwardly rectifying channel subfamily J member 1
KIR1.1, ROMK, ROMK1
Bartter syndrome, Hypertension

127
Potassium inwardly rectifying channel subfamily J member 2
ATFB9, HHBIRK1, HHIRK1, IRK1, KIR2.1, LQT7, SQT3
Andersen-tawil syndrome, Cardiac arrhythmias, Atrial fibrillation, Brugada syndrome, Cardiac arrhythmia, Catecholaminergic polymorphic ventricular tachycardia, Congenital heart disease, Dermatologic disorder, Desbuquois syndrome, Long qt syndrome, Hereditary atrial fibrillation, Hypertrophic cardiomyopathy, Polymorphic catecholaminergic ventricular tachycardia, Short qt syndrome, Skin disease
View all (2 more)

128
Potassium inwardly rectifying channel subfamily J member 3
GIRK1, KGA, KIR3.1
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Dental caries, Emphysema, Hereditary atrial fibrillation, Malunion fracture, Peripheral arterial disease, Schizophrenia, Substance abuse, Uveal melanoma

129
Potassium inwardly rectifying channel subfamily J member 4
HIR, HIRK2, HRK1, IRK-3, IRK3, Kir2.3
Conotruncal cardiac defect, Parkinson disease

130
Potassium inwardly rectifying channel subfamily J member 5
CIR, GIRK4, KATP1, KIR3.4, LQT13
Andersen-tawil syndrome, Atrial fibrillation, Atrial flutter, Cardioembolic stroke, Cushing syndrome, Hyperaldosteronism, Long qt syndrome, Hereditary atrial fibrillation, Hypertrophic cardiomyopathy, Sick sinus syndrome