Biology:ATP8B3
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Short description: Protein-coding gene in the species Homo sapiens
Generic protein structure example |
The human gene ATP8B3 encodes the protein ATPase, aminophospholipid transporter, class I, type 8B, member 3.[1]
Transcript
Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[1]
Protein
The protein encoded by this gene belongs to the family of P-type cation transport ATPases, and to the subfamily of aminophospholipid-transporting ATPases. The aminophospholipid translocases transport phosphatidylserine and phosphatidylethanolamine from one side of a bilayer to another. This gene encodes the member 3 of the phospholipid-transporting ATPase 8B.
References
External links
- Human ATP8B3 genome location and ATP8B3 gene details page in the UCSC Genome Browser.
Further reading
- "Differential expression of putative transbilayer amphipath transporters". Physiological Genomics 1 (3): 139–50. November 1999. doi:10.1152/physiolgenomics.1999.1.3.139. PMID 11015572.
- "FIC1, a P-type ATPase linked to cholestatic liver disease, has homologues (ATP8B2 and ATP8B3) expressed throughout the body". Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids 1633 (2): 127–31. July 2003. doi:10.1016/S1388-1981(03)00107-0. PMID 12880872.
- "Studies on Tyzzer's disease in rats". Laboratory Animals 12 (1): 1–4. January 1978. doi:10.1258/002367778780953297. PMID 146761.
- "Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry". Proceedings of the National Academy of Sciences of the United States of America 106 (18): 7501–6. May 2009. doi:10.1073/pnas.0813386106. PMID 19416921. PMC 2678639. Bibcode: 2009PNAS..106.7501S. http://pubman.mpdl.mpg.de/pubman/item/escidoc:529195/component/escidoc:532043/Scott_Genome_wide_association_PNAS_2009.pdf.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
Original source: https://en.wikipedia.org/wiki/ATP8B3.
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