Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "K"
111 to 120 of 320 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

111
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 disorders, Non-specific syndromic intellectual disability, Prostate cancer, Seizures

112
Potassium voltage-gated channel subfamily A member 4
HBK4, HK1, HPCN2, HUKII, KCNA4L, KCNA8, KV1.4, MCIDDS, PCN2
Microcephaly, Preeclampsia

113
Potassium voltage-gated channel subfamily A member 5
ATFB7, HCK1, HK2, HPCN1, KV1.5, PCN1
Atrial fibrillation, Benign neoplasm, Cardiac arrhythmia, Color vision deficiency, Atrioventricular block, Heart disease, Hereditary atrial fibrillation, Pulmonary hypertension, Mouth neoplasm, Nephrotic syndrome, Pulmonary arterial hypertension, Schizophrenia, Scoliosis

114
Potassium voltage-gated channel subfamily A member 10
Kcn1, Kv1.8
Long qt syndrome

115
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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116
Potassium voltage-gated channel subfamily C member 1
EPM7, KV3.1, KV4, NGK2
Neurodevelopmental disorder, Progressive myoclonic epilepsy, Non-specific syndromic intellectual disability

117
Kinesin family member 7
ACLS, AGBK, HLS2, JBTS12, MMEDF, UNQ340
Acrocallosal syndrome, Bardet-biedl syndrome, Cerebellar ataxia, Color vision deficiency, Desbuquois syndrome, Aplasia of the vermis, Hydrolethalus syndrome, Intellectual developmental disorder, Joubert syndrome, Male infertility testicular dysgenesis, Neurodevelopmental disorders, Nystagmus, Obesity, Orofaciodigital syndrome, Polydactyly
View all (2 more)

118
Potassium voltage-gated channel subfamily C member 3
KSHIIID, KV3.3, SCA13
Spinocerebellar ataxia

119
Potassium voltage-gated channel subfamily C member 4
C1orf30, HKSHIIIC, KSHIIIC, KV3.4
Temporal lobe epilepsy, Oropharyngeal cancer, Tuberculosis, Upper respiratory tract disorder

120
Potassium voltage-gated channel subfamily D member 2
KV4.2, RK5
Androgenetic alopecia, Eczema, Attention deficit hyperactivity disorder, Cholangiocarcinoma, Neurodevelopmental disorder, Myoclonic encephalopathy, Insomnia, Neurodevelopmental disorders, Non-specific syndromic intellectual disability, Prostate cancer, Substance abuse, Uterine fibroid