ATP9A

ATP9A
Identifiers
Aliases	ATP9A, ATPIIA, ATPase phospholipid transporting 9A (putative)
External IDs	OMIM: 609126; MGI: 1330826; HomoloGene: 69194; GeneCards: ATP9A; OMA:ATP9A - orthologs
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; ; Brodmann area 46; ; Brodmann area 23; ; orbitofrontal cortex; ; internal globus pallidus; ; entorhinal cortex; ; superior frontal gyrus; ; postcentral gyrus; ; paraflocculus of cerebellum; ; Brodmann area 10;
	Top expressed in
	perirhinal cortex; ; entorhinal cortex; ; CA3 field; ; primary visual cortex; ; dentate gyrus of hippocampal formation granule cell; ; superior frontal gyrus; ; cerebellar cortex; ; central gray substance of midbrain; ; nucleus of stria terminalis; ; dorsomedial hypothalamic nucleus;
	More reference expression data
	n/a
Gene ontology
Molecular function	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

Probable phospholipid-transporting ATPase IIA is a protein that in humans is encoded by the ATP9A gene.^[5]^[6]

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ATP9A

References

Further reading