ATP-binding cassette sub-family A member 3 is a protein that in humans is encoded by the ABCA3 gene.[5][6]
ABCA3 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | ABCA3, ATP-binding cassette, sub-family A (ABC1), member 3, ABC-C, ABC3, EST111653, LBM180, SMDP3, ATP binding cassette subfamily A member 3 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 601615 MGI: 1351617 HomoloGene: 37437 GeneCards: ABCA3 | ||||||||||||||||||||||||||||||||||||||||||||||||||
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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, White). This protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. The full transporter encoded by this gene may be involved in development of resistance to xenobiotics and engulfment during programmed cell death.[6]
Mutations in ABCA3 are associated to cataract-microcornea syndrome.[7]
It is associated with Surfactant metabolism dysfunction type 3.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.