ATP11C

Protein-coding gene in humans From Wikipedia, the free encyclopedia

ATP11C is an enzyme that in humans is encoded by the ATP11C gene.

AliasesATP11C, ATPIG, ATPIQ, ATPase phospholipid transporting 11C, HACXL
End139,945,276 bp[1]
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ATP11C
Identifiers
AliasesATP11C, ATPIG, ATPIQ, ATPase phospholipid transporting 11C, HACXL
External IDsOMIM: 300516; MGI: 1859661; HomoloGene: 27862; GeneCards: ATP11C; OMA:ATP11C - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001010986
NM_173694
NM_001353810
NM_001353811
NM_001353812

NM_001001798
NM_001037863
NM_001359002

RefSeq (protein)

NP_001010986
NP_775965
NP_001340739
NP_001340740
NP_001340741

NP_001001798
NP_001032952
NP_001345931

Location (UCSC)Chr X: 139.73 – 139.95 MbChr X: 59.27 – 59.64 Mb
PubMed search[3][4]
Wikidata
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Function

ATP11C encodes a member of the Type IV P-type ATPase family that is thought to transport or 'flip' aminophospholipids. The corresponding protein in mice is essential for the development of B cells and red blood cells,[5][6] and for the prevention of intrahepatic cholestasis.[7]

References

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