KCNJ12

GENE INFORMATION

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Gene name

KCNJ12 (HGNC Symbol)

Synonyms

hIRK1, IRK2, KCNJN1, Kir2.2, Kir2.2v

Description

potassium inwardly-rectifying channel, subfamily J, member 12 (HGNC Symbol)

Entrez gene summary

This gene encodes an inwardly rectifying K+ channel which may be blocked by divalent cations. This protein is thought to be one of multiple inwardly rectifying channels which contribute to the cardiac inward rectifier current (IK1). The gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Jul 2008]

Chromosome

17 (Chromosome progress)

Cytoband

p11.2

Chromosome location (bp)

21279509 - 21323179

Ensembl

ENSG00000184185 (version 73.37)

Entrez gene

3768

UniProt

Q14500 (UniProt - Evidence at protein level)

neXtProt

NX_Q14500

Antibodypedia

KCNJ12 antibodies
 

PROTEIN VIEW

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KCNJ12-001
 
KCNJ12-002
 
 
 
 
 

PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

KCNJ12-001 ENSP00000463778
ENST00000583088
Q14500
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Show » Show » 433 49 No 3
KCNJ12-002 ENSP00000328150
ENST00000331718
Q14500
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Show » Show » 433 49 No 3