Human (GRCh38.p14)
Description

solute carrier family 12 member 2 [Source:HGNC Symbol;Acc:HGNC:10911]

Gene Synonyms

BSC-2, BSC2, CCC1, NKCC1, PPP1R141

Location

Chromosome 5: 128,083,766-128,189,677 forward strand.

GRCh38:CM000667.2

About this gene

This gene has 8 transcripts (splice variants), 280 orthologues, 8 paralogues and is associated with 5 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000262461.7SLC12A2-20168741212aaENSP00000262461.2
 
Protein coding
CCDS4144P55011-1 NM_001046.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P4TSL:1
ENST00000343225.4SLC12A2-20255091196aaENSP00000340878.4
 
Protein coding
CCDS58965P55011-3 -GENCODE basicAPPRIS ALT2TSL:1
ENST00000628403.2SLC12A2-20836171150aaENSP00000486323.1
 
Protein coding
G3XAL9 -GENCODE basicTSL:5
ENST00000509205.5SLC12A2-20642631150aaENSP00000427109.1
 
Nonsense mediated decay
G3XAL9 -TSL:1
ENST00000507791.5SLC12A2-205555No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000504416.5SLC12A2-2043653No protein-
 
Retained intron
--TSL:1
ENST00000509616.1SLC12A2-207580No protein-
 
Retained intron
--TSL:2
ENST00000502849.1SLC12A2-203489No protein-
 
Retained intron
--TSL:2