| Entrez gene ID | | 3768 |
| Official gene symbol | | KCNJ12 |
| Full name | | potassium inwardly-rectifying channel, subfamily J, member 12 |
| Aliases | | ,FLJ14167,IRK2,KCNJN1,Kir2.2,Kir2.2v,hIRK,hIRK1,hkir2.2x,kcnj12x, |
| 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] |
| Location | | Chromosome: 17 Locus: 17p11.2 |
| Gene position | | 21279699 - 21323179 Map Viewer |
| Gene orientation | | plus |
| Gene size | | 43481 bp |
| Gene sequence |
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| OMIM ID | | 602323 |
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