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Gene : KCNK2 Homo sapiens

Name  ? potassium two pore domain channel subfamily K member 2 Cytological Location  1q41
Brief Description  potassium two pore domain channel subfamily K member 2
description  This gene encodes one of the members of the two-pore-domain background potassium channel protein family. This type of potassium channel is formed by two homodimers that create a channel that leaks potassium out of the cell to control resting membrane potential. The channel can be opened, however, by certain anesthetics, membrane stretching, intracellular acidosis, and heat. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
  • synonyms:
  • TREK,
  • K2p2.1,
  • potassium channel, two pore domain subfamily K, member 2,
  • hTREK-1c,
  • TREK-1,
  • NM_014217,
  • KCNK2,
  • TREK1,
  • TPKC1,
  • potassium channel, subfamily K, member 2,
  • OTTHUMG00000037017,
  • hTREK-1e,
  • TREK-1,
  • HGNC:6277,
  • uc001hkr.5,
  • K2p2.1,
  • AF004711
  • identifiers:
  • 3776,
  • ENSG00000082482,
  • KCNK2

Genome feature

Region: gene ? Length: 234174  
Location: 1:215002920-215237093 Cyto location: 1q41


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Gene -> HPO annotation (Human Phenotype Ontology)

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Proteins

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SNPs

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Disease

0 Diseases

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

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Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

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Expression

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Other

288 SN Ps

4 Cross References

13 Data Sets

20 Homologues

0 Located Features

90 Rna Seq Results