Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
6601 to 6610 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

6601
Potassium voltage-gated channel subfamily C member 1
EPM7, KV3.1, KV4, NGK2
Neurodevelopmental disorder, Progressive myoclonic epilepsy, Non-specific syndromic intellectual disability

6602
Potassium voltage-gated channel subfamily C member 2
DEE103, KV3.2
Attention deficit hyperactivity disorder, Developmental and epileptic encephalopathy, Neurotic disorder, Obesity, Schizophrenia, Scoliosis, Spondylosis, Substance abuse, Vascular dementia

6603
Potassium voltage-gated channel subfamily C member 3
KSHIIID, KV3.3, SCA13
Spinocerebellar ataxia

6604
Potassium voltage-gated channel subfamily C member 4
C1orf30, HKSHIIIC, KSHIIIC, KV3.4
Temporal lobe epilepsy, Oropharyngeal cancer, Upper aerodigestive tract neoplasm

6605
Potassium voltage-gated channel subfamily D member 2
KV4.2, RK5
Androgenetic alopecia, Eczema, Attention deficit hyperactivity disorder, Cholangiocarcinoma, Neurodevelopmental disorder, Myoclonic encephalopathy, Insomnia, Non-specific syndromic intellectual disability, Prostate cancer, Substance abuse, Uterine fibroid

6606
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 disorder, Prostate cancer, Spinocerebellar ataxia, Diabetes mellitus type 2

6607
Potassium voltage-gated channel subfamily E regulatory subunit 1
ISK, JLNS, JLNS2, LQT2/5, LQT5, MinK
Arrhythmogenic right ventricular cardiomyopathy, Atrial fibrillation, Cardiomyopathy, Dilated cardiomyopathy, Congenital hearing disorder, Long qt syndrome, Hereditary atrial fibrillation, Hypertrophic cardiomyopathy, Jervell and lange-nielsen syndrome, Long qt syndrome, digenic, Hearing loss

6608
Potassium voltage-gated channel subfamily E regulatory subunit 2
ATFB4, LQT5, LQT6, MIRP1
Alzheimer disease, Atrial fibrillation, Cardiac arrhythmia, Dilated cardiomyopathy, Cardiomyopathy, Cardiovascular disease, Ischemic heart disease, Obstructive pulmonary disease, Coronary artery disease, Long qt syndrome, Heart disease, Hereditary atrial fibrillation, Long qt syndrome, digenic, Migraine, Myocardial infarction
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6609
Potassium voltage-gated channel subfamily E regulatory subunit 3
BRGDA6, HOKPP, HYPP, MiRP2
Brugada syndrome, Corneal astigmatism, Long qt syndrome, Neurotic disorder, Oligodendroglioma, Ventricular fibrillation

6610
Potassium voltage-gated channel subfamily E regulatory subunit 4
MIRP3
Cardiac embolism, Cardioembolic stroke, Lymphoblastic leukemia, Oropharyngeal cancer