Human (GRCh37.p13)
Description

potassium channel, subfamily T, member 1 [Source:HGNC Symbol;Acc:18865]

Gene Synonyms

EIEE14, ENFL5, KCa4.1, KIAA1422, SLACK, bA100C15.2

Location

Chromosome 9: 138,594,031-138,684,992 forward strand.

GRCh37:CM000671.1

About this gene

This gene has 12 transcripts (splice variants), 3 paralogues and is associated with 8 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000298480.5KCNT1-20248301256aaENSP00000298480.5
 
Protein coding
C9JBV2 Q5JUK3 -GENCODE basic
ENST00000371757.2KCNT1-00247171235aaENSP00000360822.2
 
Protein coding
CCDS35175C9JBV2 Q5JUK3 NM_020822.2GENCODE basic
ENST00000487664.1KCNT1-00146951211aaENSP00000417851.1
 
Protein coding
CCDS65188G5E9V0 NM_001272003.1GENCODE basic
ENST00000263604.3KCNT1-20146781230aaENSP00000263604.3
 
Protein coding
Q5JUK3 -GENCODE basic
ENST00000491806.2KCNT1-00437831221aaENSP00000419086.2
 
Protein coding
C9JYL2 -GENCODE basic
ENST00000488444.2KCNT1-00537191235aaENSP00000419007.2
 
Protein coding
C9JZ51 -GENCODE basic
ENST00000486577.2KCNT1-00737141213aaENSP00000417578.2
 
Protein coding
C9J9Y7 -GENCODE basic
ENST00000490355.2KCNT1-00637081234aaENSP00000418003.2
 
Protein coding
C9JAX7 -GENCODE basic
ENST00000473941.1KCNT1-0101024285aaENSP00000420764.1
 
Protein coding
C9JBV2 -CDS 3' incomplete
ENST00000460750.1KCNT1-0034738122aaENSP00000418777.1
 
Nonsense mediated decay
F8WC49 --
ENST00000490363.1KCNT1-0094065No protein-
 
Retained intron
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ENST00000475008.1KCNT1-0083999No protein-
 
Retained intron
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