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Gene : KCNJ12 Homo sapiens

Name  ? potassium inwardly rectifying channel subfamily J member 12 Cytological Location  17p11.2
Brief Description  potassium inwardly rectifying channel subfamily J member 12
Description  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]
  • synonyms:
  • hIRK,
  • OTTHUMG00000132039,
  • hIRK1,
  • HGNC:6258,
  • potassium inwardly-rectifying channel, subfamily J, member 12,
  • hIRK1,
  • KCNJN1,
  • Kir2.2v,
  • Kir2.2,
  • NM_021012,
  • uc002gyv.2,
  • IRK2,
  • Kir2.2,
  • KCNJN1,
  • KCNJ12,
  • Kir2.2v,
  • L36069,
  • potassium inwardly-rectifying channel, subfamily J, inhibitor 1,
  • IRK-2,
  • kcnj12x,
  • IRK2,
  • hkir2.2x
  • identifiers:
  • 3768,
  • ENSG00000184185,
  • KCNJ12

Genome feature

Region: gene ? Length: 43514  
Location: 17:21376357-21419870 Cyto location: 17p11.2


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Disease

0 Diseases

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559 SN Ps

5 Cross References

16 Data Sets

23 Homologues

0 Located Features

97 Rna Seq Results