Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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6591 to 6600 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

6591
Potassium voltage-gated channel subfamily A member 2
DEE32, EIEE32, HBK5, HK4, HUKIV, KV1.2, MK2, NGK1, RBK2
Developmental and epileptic encephalopathy, Global developmental delay, Intellectual developmental disorder, Language development disorders, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Prostate cancer, Seizures

6592
Potassium voltage-gated channel subfamily A member 3
HGK5, HLK3, HPCN3, HUKIII, KV1.3, MK3, PCN3
Lymphoblastic leukemia, Neurodevelopmental disorder, Panic disorder, Prostate cancer

6593
Potassium voltage-gated channel subfamily A member 4
HBK4, HK1, HPCN2, HUKII, KCNA4L, KCNA8, KV1.4, MCIDDS, PCN2
Microcephaly, Preeclampsia

6594
Potassium voltage-gated channel subfamily A member 5
ATFB7, HCK1, HK2, HPCN1, KV1.5, PCN1
Atrial fibrillation, Neoplasms, Cardiac arrhythmia, Color vision deficiency, Atrioventricular block, Conduct disorder, Heart disease, Hereditary atrial fibrillation, Pulmonary hypertension, Mouth neoplasms, Nephrotic syndrome, Pulmonary arterial hypertension, Schizophrenia, Scoliosis

6595
Potassium voltage-gated channel subfamily A member 6
HBK2, KV1.6, PPP1R96
Cerebellar ataxia, Neurodevelopmental disorder, Congenital epicanthus, Esophageal atresia, Seizure, Hyperopia, Non-specific syndromic intellectual disability, Seizures

6596
Potassium voltage-gated channel subfamily A regulatory beta subunit 1
AKR6A3, KCNA1B, KV-BETA-1, Kvb1.3, hKvBeta3, hKvb3
Coronary artery disease, Temporal lobe epilepsy, Hypertension, Multinodular goiter, Prostate cancer, Willis-ekbom disease, Uterine fibroid

6597
Potassium voltage-gated channel subfamily A regulatory beta subunit 2
AKR6A5, HKvbeta2, HKvbeta2.1, HKvbeta2.2, KCNA2B, KV-BETA-2
1p36 deletion syndrome, Chromosome 1p36 deletion syndrome, Epilepsy

6598
Potassium voltage-gated channel subfamily A regulatory beta subunit 3
AKR6A9, KCNA3.1B, KCNA3B, KV-BETA-3
Attention deficit hyperactivity disorder, Prostate cancer, Substance abuse

6599
Potassium voltage-gated channel subfamily B member 1
DEE26, DRK1, Kv2.1
Anorexia nervosa, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Neurodevelopmental disorder, Developmental and epileptic encephalopathy, Epilepsy, Intellectual developmental disorder, Major depressive disorder, Neurotic disorder, Non-specific syndromic intellectual disability, Obesity, Obsessive-compulsive disorder, Schizophrenia
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6600
Potassium voltage-gated channel subfamily B member 2
KV2.2
Brain infarction, Cerebral amyloid angiopathy, Color vision deficiency, Colorectal cancer, Coronary artery disease, Dementia, Dry eye syndrome, Gastroesophageal reflux disease, Insomnia, Lewy body disease, Major depressive disorder, Metabolic syndrome, Multiple sclerosis, Neurodevelopmental disorder, Peptic ulcer disease
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