ABCA3

ABCA3
Identifiers
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
Gene location (Human) Chr. Chromosome 16 (human) Band 16p13.3 Start 2,275,881 bp End 2,340,746 bp
Gene location (Mouse) Chr. Chromosome 17 (mouse) Band 17|17 A3.3 Start 24,570,924 bp End 24,629,175 bp
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in lower lobe of lung upper lobe of lung upper lobe of left lung frontal pole prefrontal cortex inferior olivary nucleus middle temporal gyrus Brodmann area 10 middle frontal gyrus Brodmann area 9 Top expressed in left lung lobe right lung right lung lobe kidney facial motor nucleus trigeminal ganglion olfactory epithelium prostate motor neuron fossa More reference expression data BioGPS More reference expression data
Gene ontology Molecular function ATPase-coupled transmembrane transporter activity nucleotide binding ATPase activity ATP binding transporter activity lipid transporter activity Cellular component lamellar body membrane integral component of membrane plasma membrane membrane alveolar lamellar body membrane alveolar lamellar body extracellular space intracellular membrane-bounded organelle Biological process lipid transport response to glucocorticoid transmembrane transport transport Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 21 27410 Ensembl ENSG00000167972 ENSMUSG00000024130 UniProt Q99758 Q8R420 RefSeq (mRNA) NM_001089 NM_001039581 NM_013855 RefSeq (protein) NP_001080 NP_001034670 NP_038883 Location (UCSC) Chr 16: 2.28 – 2.34 Mb Chr 17: 24.57 – 24.63 Mb PubMed search
Wikidata
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ATP-binding cassette sub-family A member 3 is a protein that in humans is encoded by the ABCA3 gene.

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.

Clinical significance

Mutations in ABCA3 are associated to cataract-microcornea syndrome.

It is associated with Surfactant metabolism dysfunction type 3.

See also

• ATP-binding cassette transporter

Further reading

• Connors TD, Van Raay TJ, Petry LR, et al. (1997). "The cloning of a human ABC gene (ABC3) mapping to chromosome 16p13.3". Genomics. 39 (2): 231–4. doi:10.1006/geno.1996.4500. PMID 9027511.
• Yamano G, Funahashi H, Kawanami O, et al. (2001). "ABCA3 is a lamellar body membrane protein in human lung alveolar type II cells". FEBS Lett. 508 (2): 221–5. doi:10.1016/S0014-5793(01)03056-3. PMID 11718719. S2CID 24575651.
• Mulugeta S, Gray JM, Notarfrancesco KL, et al. (2002). "Identification of LBM180, a lamellar body limiting membrane protein of alveolar type II cells, as the ABC transporter protein ABCA3". J. Biol. Chem. 277 (25): 22147–55. doi:10.1074/jbc.M201812200. PMID 11940594.
• Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
• Shulenin S, Nogee LM, Annilo T, et al. (2004). "ABCA3 gene mutations in newborns with fatal surfactant deficiency". N. Engl. J. Med. 350 (13): 1296–303. doi:10.1056/NEJMoa032178. PMID 15044640.
• Nagata K, Yamamoto A, Ban N, et al. (2004). "Human ABCA3, a product of a responsible gene for abca3 for fatal surfactant deficiency in newborns, exhibits unique ATP hydrolysis activity and generates intracellular multilamellar vesicles". Biochem. Biophys. Res. Commun. 324 (1): 262–8. doi:10.1016/j.bbrc.2004.09.043. PMID 15465012.
• Wulf GG, Modlich S, Inagaki N, et al. (2006). "ABC transporter ABCA3 is expressed in acute myeloid leukemia blast cells and participates in vesicular transport". Haematologica. 89 (11): 1395–7. PMID 15531465.
• Kimura K, Wakamatsu A, Suzuki Y, et al. (2006). "Diversification of transcriptional modulation: Large-scale identification and characterization of putative alternative promoters of human genes". Genome Res. 16 (1): 55–65. doi:10.1101/gr.4039406. PMC 1356129. PMID 16344560.
• Cheong N, Madesh M, Gonzales LW, et al. (2006). "Functional and trafficking defects in ATP binding cassette A3 mutants associated with respiratory distress syndrome". J. Biol. Chem. 281 (14): 9791–800. doi:10.1074/jbc.M507515200. PMID 16415354.
• Steinbach D, Gillet JP, Sauerbrey A, et al. (2007). "ABCA3 as a possible cause of drug resistance in childhood acute myeloid leukemia". Clin. Cancer Res. 12 (14 Pt 1): 4357–63. doi:10.1158/1078-0432.CCR-05-2587. PMID 16857811.
• Matsumura Y, Ban N, Ueda K, Inagaki N (2006). "Characterization and classification of ATP-binding cassette transporter ABCA3 mutants in fatal surfactant deficiency". J. Biol. Chem. 281 (45): 34503–14. doi:10.1074/jbc.M600071200. PMID 16959783.
• Piehler AP, Wenzel JJ, Olstad OK, et al. (2006). "The human ortholog of the rodent testis-specific ABC transporter Abca17 is a ubiquitously expressed pseudogene (ABCA17P) and shares a common 5' end with ABCA3". BMC Mol. Biol. 7: 28. doi:10.1186/1471-2199-7-28. PMC 1579226. PMID 16968533.
• Saugstad OD, Hansen TW, Rønnestad A, et al. (2007). "Novel mutations in the gene encoding ATP binding cassette protein member A3 (ABCA3) resulting in fatal neonatal lung disease". Acta Paediatr. 96 (2): 185–90. doi:10.1111/j.1651-2227.2007.00016.x. PMID 17429902. S2CID 22025230.
• Matsumura Y, Sakai H, Sasaki M, et al. (2007). "ABCA3-mediated choline-phospholipids uptake into intracellular vesicles in A549 cells". FEBS Lett. 581 (17): 3139–44. doi:10.1016/j.febslet.2007.05.078. PMID 17574245. S2CID 19618400.
• Bullard JE, Nogee LM (2007). "Heterozygosity for ABCA3 mutations modifies the severity of lung disease associated with a surfactant protein C gene (SFTPC) mutation". Pediatr. Res. 62 (2): 176–9. doi:10.1203/PDR.0b013e3180a72588. PMID 17597647.

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.