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KCNJ10 information


KCNJ10
Identifiers
AliasesKCNJ10, BIRK-10, KCNJ13-PEN, KIR1.2, KIR4.1, SESAME, potassium voltage-gated channel subfamily J member 10, potassium inwardly rectifying channel subfamily J member 10
External IDsOMIM: 602208; MGI: 1194504; HomoloGene: 1689; GeneCards: KCNJ10; OMA:KCNJ10 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_002241

NM_001039484
NM_020269

RefSeq (protein)

NP_002232

NP_001034573

Location (UCSC)Chr 1: 160 – 160.07 MbChr 1: 172.17 – 172.2 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

ATP-sensitive inward rectifier potassium channel 10 is a protein that in humans is encoded by the KCNJ10 gene.[5][6][7][8]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000177807 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000044708 – Ensembl, 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. ^ Tada Y, Horio Y, Takumi T, Terayama M, Tsuji L, Copeland NG, et al. (November 1997). "Assignment of the glial inwardly rectifying potassium channel KAB-2/Kir4.1 (Kcnj10) gene to the distal region of mouse chromosome 1". Genomics. 45 (3): 629–30. doi:10.1006/geno.1997.4957. PMID 9367690.
  6. ^ Shuck ME, Piser TM, Bock JH, Slightom JL, Lee KS, Bienkowski MJ (January 1997). "Cloning and characterization of two K+ inward rectifier (Kir) 1.1 potassium channel homologs from human kidney (Kir1.2 and Kir1.3)". The Journal of Biological Chemistry. 272 (1): 586–93. doi:10.1074/jbc.272.1.586. PMID 8995301.
  7. ^ Kubo Y, Adelman JP, Clapham DE, Jan LY, Karschin A, Kurachi Y, et al. (December 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.
  8. ^ "Entrez Gene: KCNJ10 potassium inwardly-rectifying channel, subfamily J, member 10".

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KCNJ10

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rectifier potassium channel 10 is a protein that in humans is encoded by the KCNJ10 gene. This gene encodes a member of the inward rectifier-type potassium...

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goiter. Ataxia is a hereditary condition in the breed. A mutation in the KCNJ10 gene, which has been identified in the Jack Russell Terrier and Parson Russell...

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genetic disorder caused by mutations in the KCNJ10 gene, as discovered by Bockenhauer and co-workers. The KCNJ10 gene encodes the K+ channel Kir4.1 (allowing...

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seizures are often seen alongside the condition. A 2014 study identified the KCNJ10 gene as being responsible for the spinocerebellar ataxia accompanied by...

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seizures are often seen alongside the condition. A 2014 study identified the KCNJ10 gene as being responsible for the spinocerebellar ataxia accompanied by...

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seizures are often seen alongside the condition. A 2014 study identified the KCNJ10 gene as being responsible for the spinocerebellar ataxia accompanied by...

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include the syndromes caused by genetic mutations in SLC12A3, CLNCKB, BSND, KCNJ10, FXYD2, HNF1B or PCBD1. In these diseases, the hypomagnesemia is accompanied...

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Index of biophysics articles

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KCNF1 KCNG1 KCNG2 KCNG3 KCNG4 KCNH3 KCNH4 KCNH6 KCNH7 KCNH8 KCNIP1 KCNIP4 KCNJ10 KCNJ12 KCNJ13 KCNJ14 KCNJ15 KCNJ16 KCNJ3 KCNJ4 KCNJ5 KCNJ6 KCNJ8 KCNJ9 KCNK1...

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(May 2009). "Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations". The New England Journal of Medicine. 360 (19): 1960–1970. doi:10...

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Denoyelle F, Marlin S (September 2010). "Screening of SLC26A4, FOXI1 and KCNJ10 genes in unilateral hearing impairment with ipsilateral enlarged vestibular...

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WNT4 Sertoli cell-only syndrome; 400042; ZNF148 SESAME syndrome; 612780; KCNJ10 Severe combined immunodeficiency due to ADA deficiency; 102700; ADA Severe...

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