ATP9A

ATP9A
Identifiers
Aliases	ATP9A, ATPIIA, ATPase phospholipid transporting 9A (putative)
External IDs	OMIM: 609126 MGI: 1330826 HomoloGene: 69194 GeneCards: ATP9A
Gene location (Human)
Chr.	Chromosome 20 (human)[1]
End	51,768,390 bp[1]
Gene location (Mouse)
Chr.	Chromosome 2 (mouse)[2]
End	168,742,409 bp[2]
Gene ontology
Molecular function	• GO:0004012 ATPase-coupled intramembrane lipid transporter activity; • nucleotide binding; • ATP binding; • magnesium ion binding; • hydrolase activity; • metal ion binding;
Cellular component	• perinuclear region of cytoplasm; • integral component of membrane; • recycling endosome; • endosome; • trans-Golgi network; • cell membrane; • Golgi apparatus; • early endosome; • early endosome membrane; • membrane;
Biological process	• phospholipid transport; • endocytosis; • retrograde vesicle-mediated transport, Golgi to ER; • phospholipid translocation;
	Sources:Amigo / QuickGO
Orthologs
	10079
	11981
	ENSG00000054793
	ENSMUSG00000027546
	O75110
	O70228
	NM_006045
	NM_001289445; NM_001289446; NM_015731; NM_001354977; NM_001354978
	NP_006036
	NP_001276374; NP_001276375; NP_056546; NP_001341906; NP_001341907
	Wikidata
View/Edit Human	View/Edit Mouse

ATPase phospholipid transporting 9A (putative) is a protein that in humans is encoded by the ATP9A gene. [5]

References

GRCh38: Ensembl release 89: ENSG00000054793 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000027546 - 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.
"Entrez Gene: ATPase phospholipid transporting 9A (putative)". Retrieved 2016-10-04.

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