KCNT1
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 9[14]
- Cytogenetic location
- 9q34.3[19]
- Expressed in
- right hemisphere of cerebellum, right frontal lobe, Brodmann area 9, anterior cingulate cortex, gastrocnemius muscle, putamen, muscle of thigh, prefrontal cortex, caudate nucleus, spleen[20][21][22][23][24][25][26][27][28]
- Found in taxon
- Homo sapiens[13]
- Genetic association
- autosomal dominant nocturnal frontal lobe epilepsy 5, epilepsy in children, epileptic encephalopathy, early infantile, 14[15][16][17]
- HomoloGene ID
- 11055[3]
- Strand orientation
- forward strand[18]
🏷️ Also known as
en bA100C15.2
en DEE14
en EIEE14
en ENFL5
en KCa4.1
en KCNT1
en potassium sodium-activated channel subfamily T member 1
en SLACK
en Slo2.2
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000107147
- Ensembl transcript ID
- ENST00000631193, ENST00000263604, ENST00000371757, ENST00000460750, ENST00000473941, ENST00000475008, ENST00000486577, ENST00000487664, ENST00000488444, ENST00000490355, ENST00000490363, ENST00000491806, ENST00000628528, ENST00000630792, ENST00000631073, ENST00000636003, ENST00000636274, ENST00000636613, ENST00000636961, ENST00000636995, ENST00000637018, ENST00000637082, ENST00000637090, ENST00000637668, ENST00000637798, ENST00000638022, ENST00000638123, ENST00000675090, ENST00000674572, ENST00000675102, ENST00000675399, ENST00000676421
- Entrez Gene ID
- 57582
- Exact match
- identifiers.org
- Freebase ID
- /m/056f9vd
- HGNC ID
- 18865
- HGNC gene symbol
- KCNT1
- OMIM ID
- 608167
- RefSeq RNA ID
- XM_011518881, NM_001272003, NM_020822, XM_011518878, XM_011518879, XM_011518880, XM_017014931, XM_017014932, XM_017014933, XM_024447617, XM_024447618
- UMLS CUI
- C1425836
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