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)
End	51,768,390 bp
Gene location (Mouse)
Chr.	Chromosome 2 (mouse)
End	168,584,329 bp
RNA expression pattern
	Top expressed in
	middle temporal gyrus; ; prosencephalon; ; caudate nucleus; ; Brodmann area 23; ; Brodmann area 46; ; internal globus pallidus; ; orbitofrontal cortex; ; dorsolateral prefrontal cortex; ; brain;
	More reference expression data
	n/a
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; plasma membrane; Golgi apparatus; early endosome; early endosome membrane; membrane;
Biological process	phospholipid transport; endocytosis; retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum; 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[]

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000054793 - Ensembl, May 2017
^ ^a ^b ^c 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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