ATP9A

ATP9A
Identifiers
Aliases	ATP9A, ATPIIA, ATPase phospholipid transporting 9A (putative)
External IDs	MGI: 1330826 HomoloGene: 69194 GeneCards: ATP9A
Gene location (Human)
Chr.	Chromosome 20 (human)[1]
End	51,768,634 bp[1]
Gene location (Mouse)
Chr.	Chromosome 2 (mouse)[2]
End	168,742,409 bp[2]
Gene ontology
Molecular function	• phospholipid-translocating ATPase 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 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

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.