Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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6611 to 6620 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

6611
Potassium voltage-gated channel subfamily E regulatory subunit 5
KCNE1L
Brugada syndrome

6612
Potassium voltage-gated channel modifier subfamily F member 1
IK8, KCNF, KV5.1, kH1
Alzheimer disease, Anxiety disorder, Gastric ulcer, Gastritis, Major depressive disorder, Moyamoya angiopathy, Ocular hypotension

6613
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

6614
Potassium voltage-gated channel modifier subfamily G member 2
KCNF2, KV6.2
Amyotrophic lateral sclerosis, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Endometriosis, Insomnia, Major depressive disorder, Neurotic disorder, Obesity, Oligodendroglioma, Psychiatric disorders, Schizophrenia, Substance abuse

6615
Potassium voltage-gated channel modifier subfamily G member 3
KV10.1, KV6.3
Insomnia

6616
Potassium voltage-gated channel modifier subfamily G member 4
KV6.3, KV6.4
Alzheimer disease, Scoliosis

6617
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 neoplasms, 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 (13 more)

6618
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 neoplasms, Conduction disorder of the heart, Congenital short qt syndrome, Haploinsufficiency, Diverticular disease, Long qt syndrome, Gout, Hypertrophic cardiomyopathy
View all (12 more)

6619
Potassium voltage-gated channel subfamily H member 3
BEC1, ELK2, Kv12.2
Attention deficit hyperactivity disorder, Neurodevelopmental disorder, Renal cell carcinoma, Schizophrenia, Tourette syndrome

6620
Potassium voltage-gated channel subfamily H member 5
DEE112, EAG2, H-EAG2, Kv10.2, hEAG2
Alzheimer disease, Aneurysm, Aortic aneurysm, Color vision deficiency, Conotruncal cardiac defect, Developmental and epileptic encephalopathy, Gastroesophageal reflux disease, Major depressive disorder, Metabolic syndrome, Diabetes mellitus type 2