regulation of long-term neuronal synaptic plasticity
central nervous system myelination
regulation of membrane potential
regulation of ion transmembrane transport
ion transport
potassium ion transport
potassium ion homeostasis
potassium ion transmembrane transport
glutamate reuptake
regulation of resting membrane potential
oligodendrocyte development
visual perception
adult walking behavior
potassium ion import across plasma membrane
Sources:Amigo / QuickGO
Orthologs
Species
Human
Mouse
Entrez
3766
16513
Ensembl
ENSG00000177807
ENSMUSG00000044708
UniProt
P78508
Q9JM63
RefSeq (mRNA)
NM_002241
NM_001039484 NM_020269
RefSeq (protein)
NP_002232
NP_001034573
Location (UCSC)
Chr 1: 160 – 160.07 Mb
Chr 1: 172.17 – 172.2 Mb
PubMed search
[3]
[4]
Wikidata
View/Edit Human
View/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]
^ abcGRCh38: Ensembl release 89: ENSG00000177807 – Ensembl, May 2017
^ abcGRCm38: Ensembl release 89: ENSMUSG00000044708 – Ensembl, May 2017
^"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^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.
^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.
^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.
^"Entrez Gene: KCNJ10 potassium inwardly-rectifying channel, subfamily J, member 10".
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...
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...
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...
seizures are often seen alongside the condition. A 2014 study identified the KCNJ10 gene as being responsible for the spinocerebellar ataxia accompanied by...
seizures are often seen alongside the condition. A 2014 study identified the KCNJ10 gene as being responsible for the spinocerebellar ataxia accompanied by...
seizures are often seen alongside the condition. A 2014 study identified the KCNJ10 gene as being responsible for the spinocerebellar ataxia accompanied by...
include the syndromes caused by genetic mutations in SLC12A3, CLNCKB, BSND, KCNJ10, FXYD2, HNF1B or PCBD1. In these diseases, the hypomagnesemia is accompanied...
(May 2009). "Epilepsy, ataxia, sensorineural deafness, tubulopathy, and KCNJ10 mutations". The New England Journal of Medicine. 360 (19): 1960–1970. doi:10...
Denoyelle F, Marlin S (September 2010). "Screening of SLC26A4, FOXI1 and KCNJ10 genes in unilateral hearing impairment with ipsilateral enlarged vestibular...
WNT4 Sertoli cell-only syndrome; 400042; ZNF148 SESAME syndrome; 612780; KCNJ10 Severe combined immunodeficiency due to ADA deficiency; 102700; ADA Severe...