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KCNJ12

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(Redirected from Kir2.2) Protein-coding gene in the species Homo sapiens
KCNJ12
Identifiers
AliasesKCNJ12, IRK-2, IRK2, KCNJN1, Kir2.2, Kir2.2v, hIRK, hIRK1, hkir2.2x, kcnj12x, potassium voltage-gated channel subfamily J member 12, potassium inwardly rectifying channel subfamily J member 12
External IDsOMIM: 602323; MGI: 108495; HomoloGene: 7793; GeneCards: KCNJ12; OMA:KCNJ12 - orthologs
Gene location (Human)
Chromosome 17 (human)
Chr.Chromosome 17 (human)
Chromosome 17 (human)Genomic location for KCNJ12Genomic location for KCNJ12
Band17p11.2Start21,376,357 bp
End21,419,870 bp
Gene location (Mouse)
Chromosome 11 (mouse)
Chr.Chromosome 11 (mouse)
Chromosome 11 (mouse)Genomic location for KCNJ12Genomic location for KCNJ12
Band11 B2|11 37.96 cMStart60,913,390 bp
End60,961,957 bp
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • Skeletal muscle tissue of rectus abdominis

  • cerebellar vermis

  • muscle of thigh

  • cerebellar hemisphere

  • right hemisphere of cerebellum

  • gastrocnemius muscle

  • quadriceps femoris muscle

  • vastus lateralis muscle

  • tibialis anterior muscle

  • Skeletal muscle tissue of biceps brachii
Top expressed in
  • muscle of thigh

  • cerebellar cortex

  • lumbar spinal ganglion

  • sternocleidomastoid muscle

  • lens

  • triceps brachii muscle

  • skeletal muscle tissue

  • knee joint

  • temporal muscle

  • quadriceps femoris muscle
More reference expression data
BioGPS


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

3768

16515

Ensembl

ENSG00000184185

ENSMUSG00000042529

UniProt

Q14500

P52187

RefSeq (mRNA)

NM_021012

NM_001267593
NM_010603

RefSeq (protein)

NP_066292

NP_001254522
NP_034733

Location (UCSC)Chr 17: 21.38 – 21.42 MbChr 11: 60.91 – 60.96 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

ATP-sensitive inward rectifier potassium channel 12 is a lipid-gated ion channel that in humans is encoded by the KCNJ12 gene.

Function

This gene encodes an inwardly rectifying K channel that may be blocked by divalent cations. This protein is thought to be one of multiple inwardly rectifying channels that contribute to the cardiac inward rectifier current (IK1). The gene is located within the Smith–Magenis syndrome region on chromosome 17.

Interactions

KCNJ12 has been shown to interact with:

See also

References

  1. ^ GRCh38: Ensembl release 89: ENSG00000184185Ensembl, May 2017
  2. ^ GRCm38: Ensembl release 89: ENSMUSG00000042529Ensembl, 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. Hansen, SB (May 2015). "Lipid agonism: The PIP2 paradigm of ligand-gated ion channels". Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1851 (5): 620–8. doi:10.1016/j.bbalip.2015.01.011. PMC 4540326. PMID 25633344.
  6. Wible BA, De Biasi M, Majumder K, Taglialatela M, Brown AM (Mar 1995). "Cloning and functional expression of an inwardly rectifying K+ channel from human atrium". Circulation Research. 76 (3): 343–50. doi:10.1161/01.res.76.3.343. PMID 7859381.
  7. Kaibara M, Ishihara K, Doi Y, Hayashi H, Ehara T, Taniyama K (Nov 2002). "Identification of human Kir2.2 (KCNJ12) gene encoding functional inward rectifier potassium channel in both mammalian cells and Xenopus oocytes". FEBS Letters. 531 (2): 250–4. Bibcode:2002FEBSL.531..250K. doi:10.1016/S0014-5793(02)03512-3. PMID 12417321. S2CID 46515689.
  8. 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.
  9. ^ "Entrez Gene: KCNJ12 potassium inwardly-rectifying channel, subfamily J, member 12".
  10. ^ Leonoudakis D, Conti LR, Anderson S, Radeke CM, McGuire LM, Adams ME, Froehner SC, Yates JR, Vandenberg CA (May 2004). "Protein trafficking and anchoring complexes revealed by proteomic analysis of inward rectifier potassium channel (Kir2.x)-associated proteins". The Journal of Biological Chemistry. 279 (21): 22331–46. doi:10.1074/jbc.M400285200. PMID 15024025.
  11. ^ Leonoudakis D, Conti LR, Radeke CM, McGuire LM, Vandenberg CA (Apr 2004). "A multiprotein trafficking complex composed of SAP97, CASK, Veli, and Mint1 is associated with inward rectifier Kir2 potassium channels". The Journal of Biological Chemistry. 279 (18): 19051–63. doi:10.1074/jbc.M400284200. PMID 14960569.
  12. Leonoudakis D, Mailliard W, Wingerd K, Clegg D, Vandenberg C (Mar 2001). "Inward rectifier potassium channel Kir2.2 is associated with synapse-associated protein SAP97". Journal of Cell Science. 114 (Pt 5): 987–98. doi:10.1242/jcs.114.5.987. PMID 11181181.

Further reading

External links

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

Membrane transport protein: ion channels (TC 1A)
Ca: Calcium channel
Ligand-gated
Voltage-gated
Na: Sodium channel
Constitutively active
Proton-gated
Voltage-gated
K: Potassium channel
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


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