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KCNJ9

From Wikipedia, the free encyclopedia
Protein-coding gene in the species Homo sapiens
KCNJ9
Identifiers
Aliases KCNJ9 , GIRK3, KIR3.3, potassium voltage-gated channel subfamily J member 9, potassium inwardly rectifying channel subfamily J member 9
External IDsOMIM: 600932; MGI: 108007; HomoloGene: 37989; GeneCards: KCNJ9; OMA:KCNJ9 - orthologs
Gene location (Human)
Chromosome 1 (human)
Chr. Chromosome 1 (human) [1]
Band 1q23.2Start160,081,538 bp [1]
End160,090,563 bp [1]
Gene location (Mouse)
Chromosome 1 (mouse)
Chr. Chromosome 1 (mouse)[2]
Band 1 H3|1 79.66 cMStart172,148,068 bp [2]
End172,156,885 bp [2]
RNA expression pattern
Bgee
Human Mouse (ortholog)
  • middle temporal gyrus

  • Brodmann area 23

  • primary visual cortex

  • right hemisphere of cerebellum

  • right frontal lobe

  • lateral nuclear group of thalamus

  • dorsolateral prefrontal cortex

  • superior frontal gyrus

  • prefrontal cortex

  • postcentral gyrus
  • cerebellar vermis

  • medial dorsal nucleus

  • lateral geniculate nucleus

  • lobe of cerebellum

  • neural layer of retina

  • medial geniculate nucleus

  • cingulate gyrus

  • primary motor cortex

  • perirhinal cortex

  • entorhinal cortex
More reference expression data
BioGPS
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

3765

16524

Ensembl

ENSG00000162728

ENSMUSG00000038026

UniProt

Q92806

P48543

RefSeq (mRNA)

NM_004983

NM_008429
NM_001360808

RefSeq (protein)

NP_004974

NP_032455
NP_001347737

Location (UCSC)Chr 1: 160.08 – 160.09 Mb Chr 1: 172.15 – 172.16 Mb
PubMed search[3] [4]
Wikidata

G protein-activated inward rectifier potassium channel 3 is a protein that in humans is encoded by the KCNJ9 gene.[5] [6] [7]

Function

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Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, is controlled by G-proteins. It associates with another G-protein-activated potassium channel to form a heteromultimeric pore-forming complex.[7]

Interactions

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KCNJ9 has been shown to interact with KCNJ6.[8] [9]

See also

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References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000162728Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000038026Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Lesage F, Fink M, Barhanin J, Lazdunski M, Mattéi MG (Oct 1995). "Assignment of human G-protein-coupled inward rectifier K+ channel homolog GIRK3 gene to chromosome 1q21-q23". Genomics. 29 (3): 808–9. doi:10.1006/geno.1995.9928. PMID 8575783.
  6. ^ Kubo Y, Adelman JP, Clapham DE, Jan LY, Karschin A, Kurachi Y, Lazdunski M, Nichols CG, Seino S, Vandenberg CA (Dec 2005). "International Union of Pharmacology. LIV. Nomenclature and molecular relationships of inwardly rectifying potassium channels". Pharmacological Reviews. 57 (4): 509–26. doi:10.1124/pr.57.4.11. PMID 16382105. S2CID 11588492.
  7. ^ a b "Entrez Gene: KCNJ9 potassium inwardly-rectifying channel, subfamily J, member 9".
  8. ^ Jelacic TM, Kennedy ME, Wickman K, Clapham DE (Nov 2000). "Functional and biochemical evidence for G-protein-gated inwardly rectifying K+ (GIRK) channels composed of GIRK2 and GIRK3". The Journal of Biological Chemistry. 275 (46): 36211–6. doi:10.1074/jbc.M007087200 . PMID 10956667.
  9. ^ Lavine N, Ethier N, Oak JN, Pei L, Liu F, Trieu P, Rebois RV, Bouvier M, Hebert TE, Van Tol HH (Nov 2002). "G protein-coupled receptors form stable complexes with inwardly rectifying potassium channels and adenylyl cyclase". The Journal of Biological Chemistry. 277 (48): 46010–9. doi:10.1074/jbc.M205035200 . PMID 12297500.

Further reading

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[edit ]
Ligand-gated
Voltage-gated
Constitutively active
Proton-gated
Voltage-gated
Calcium-activated
Inward-rectifier
Tandem pore domain
Voltage-gated
Miscellaneous
Cl: Chloride channel
H+: Proton channel
M+: CNG cation channel
M+: TRP cation channel
H2O (+ solutes): Porin
Cytoplasm: Gap junction
By gating mechanism
Ion channel class
see also disorders

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

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