ABCA3
Template:PBB ATP-binding cassette sub-family A member 3 is a protein that in humans is encoded by the ABCA3 gene.[1][2]
Clinical significance
Mutations in ABCA3 are associated to Template:SWL.[3]
It is associated with Surfactant metabolism dysfunction type 3.
See also
References
- ^ Klugbauer N, Hofmann F (Sep 1996). "Primary structure of a novel ABC transporter with a chromosomal localization on the band encoding the multidrug resistance-associated protein". FEBS Lett. 391 (1–2): 61–5. doi:10.1016/0014-5793(96)00700-4. PMID 8706931.
- ^ "Entrez Gene: ABCA3 ATP-binding cassette, sub-family A (ABC1), member 3".
- ^ Attention: This template ({{cite pmid}}) is deprecated. To cite the publication identified by PMID 25406294, please use {{cite journal}} with
|pmid=25406294instead.
Further reading
External links
- ABCA3+protein,+human at the U.S. National Library of Medicine Medical Subject Headings (MeSH)
- ABCA3 human gene location in the UCSC Genome Browser.
- ABCA3 human gene details in the UCSC Genome Browser.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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