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Gene : KCNJ5 Homo sapiens

Name  ? potassium inwardly rectifying channel subfamily J member 5 Cytological Location  11q24.3
Brief Description  potassium inwardly rectifying channel subfamily J member 5
Description  This gene encodes an integral membrane protein which belongs to one of seven subfamilies of inward-rectifier potassium channel proteins called potassium channel subfamily J. The encoded protein is a subunit of the potassium channel which is homotetrameric. It is controlled by G-proteins and has a greater tendency to allow potassium to flow into a cell rather than out of a cell. Naturally occurring mutations in this gene are associated with aldosterone-producing adenomas. [provided by RefSeq, Aug 2017]
  • synonyms:
  • potassium inwardly-rectifying channel, subfamily J, member 5,
  • KATP1,
  • LQT13,
  • D50134,
  • KATP1,
  • KCNJ5,
  • LQT13,
  • HGNC:6266,
  • CIR,
  • OTTHUMG00000165795,
  • GIRK4,
  • uc001qet.4,
  • NM_000890,
  • GIRK4,
  • CIR,
  • G protein-activated inward rectifier potassium channel 4,
  • Kir3.4,
  • KIR3.4
  • identifiers:
  • 3762,
  • ENSG00000120457,
  • KCNJ5

Genome feature

Region: gene ? Length: 29808  
Location: 11:128891356-128921163 Cyto location: 11q24.3

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2 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

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240 SN Ps

5 Cross References

19 Data Sets

7 Homologues

0 Located Features

97 Rna Seq Results