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Human (GRCh37.p13)
Description

potassium channel, subfamily T, member 2 [Source:HGNC Symbol;Acc:18866]

Gene Synonyms

KCa4.2, SLICK, SLO2.1

Location

Chromosome 1: 196,194,909-196,578,355 reverse strand.

GRCh37:CM000663.1

About this gene

This gene has 8 transcripts (splice variants), 3 paralogues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000367433.5KCNT2-00258831111aaENSP00000356403.5
 
Protein coding
Q6UVM3 NM_001287819
NM_198503
NP_001274748
NP_940905
GENCODE basic
ENST00000367431.4KCNT2-20157531069aaENSP00000356401.4
 
Protein coding
G8JLE3 -GENCODE basic
ENST00000294725.9KCNT2-00144091135aaENSP00000294725.8
 
Protein coding
CCDS1384A9LNM6 Q6UVM3 -GENCODE basic
ENST00000609185.1KCNT2-00636221068aaENSP00000476657.1
 
Protein coding
-NP_001274749
GENCODE basic
ENST00000451324.2KCNT2-2023146370aaENSP00000405474.2
 
Protein coding
Q3SY61 -GENCODE basic
ENST00000466914.2KCNT2-004695169aaENSP00000477456.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000498426.1KCNT2-0035157No protein-
 
Processed transcript
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ENST00000610076.1KCNT2-0053462No protein-
 
Processed transcript
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Gene-based displays