ABCA10

ABCA10
Identifiers
Aliases	ABCA10, EST698739, ATP binding cassette subfamily A member 10
External IDs	OMIM: 612508 HomoloGene: 122432 GeneCards: ABCA10
Gene location (Human)
Chr.	Chromosome 17 (human)[1]
End	69,244,846 bp[1]
Gene ontology
Molecular function	• ATP binding; • nucleotide binding; • ATPase activity; • ATPase activity, coupled to transmembrane movement of substances; • lipid transporter activity;
Cellular component	• integral component of membrane; • intracellular membrane-bounded organelle; • membrane;
Biological process	• lipid transport; • transmembrane transport; • ATP hydrolysis coupled ion transmembrane transport;
	Sources:Amigo / QuickGO
Orthologs
	10349
	n/a
	ENSG00000154263
	n/a
	Q8WWZ4
	n/a
	NM_080282; NM_001377321
	n/a
	NP_525021; NP_001364250
	n/a
	Wikidata
View/Edit Human

ATP binding cassette subfamily A member 10 is a protein that in humans is encoded by the ABCA10 gene. [3]

Function

The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, and White). This encoded protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. This gene is clustered among 4 other ABC1 family members on 17q24, but neither the substrate nor the function of this gene is known. [provided by RefSeq, Jul 2008].

References

GRCh38: Ensembl release 89: ENSG00000154263 - Ensembl, May 2017
"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Entrez Gene: ATP binding cassette subfamily A member 10". Retrieved 2018-07-27.

ABCA10

Function

References

Further reading