P3 protein is a protein that in humans is encoded by the SLC10A3 gene.[5][6]
This gene maps to a GC-rich region of the X chromosome and was identified by its proximity to a CpG island. It is thought to be a housekeeping gene.[6]
See also
References
- ^ a b c GRCh38: Ensembl release 89: ENSG00000126903 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000032806 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ Chen EY, Zollo M, Mazzarella R, Ciccodicola A, Chen CN, Zuo L, Heiner C, Burough F, Repetto M, Schlessinger D, D'Urso M (Jun 1997). "Long-range sequence analysis in Xq28: thirteen known and six candidate genes in 219.4 kb of high GC DNA between the RCP/GCP and G6PD loci". Hum Mol Genet. 5 (5): 659–68. doi:10.1093/hmg/5.5.659. PMID 8733135.
- ^ a b "Entrez Gene: SLC10A3 solute carrier family 10 (sodium/bile acid cotransporter family), member 3".
Further reading
- Mehrle A, Rosenfelder H, Schupp I, et al. (2006). "The LIFEdb database in 2006". Nucleic Acids Res. 34 (Database issue): D415–8. doi:10.1093/nar/gkj139. PMC 1347501. PMID 16381901.
- Wiemann S, Arlt D, Huber W, et al. (2004). "From ORFeome to biology: a functional genomics pipeline". Genome Res. 14 (10B): 2136–44. doi:10.1101/gr.2576704. PMC 528930. PMID 15489336.
- 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.
- Simpson JC, Wellenreuther R, Poustka A, et al. (2001). "Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing". EMBO Rep. 1 (3): 287–92. doi:10.1093/embo-reports/kvd058. PMC 1083732. PMID 11256614.
- Hartley JL, Temple GF, Brasch MA (2001). "DNA cloning using in vitro site-specific recombination". Genome Res. 10 (11): 1788–95. doi:10.1101/gr.143000. PMC 310948. PMID 11076863.
- Alcalay M, Toniolo D (1988). "CpG islands of the X chromosome are gene associated". Nucleic Acids Res. 16 (20): 9527–43. doi:10.1093/nar/16.20.9527. PMC 338761. PMID 3186440.
- Faust CJ, Levinson B, Gitschier J, Herman GE (1992). "Extension of the physical map in the region of the mouse X chromosome homologous to human Xq28 and identification of an exception to conserved linkage". Genomics. 13 (4): 1289–95. doi:10.1016/0888-7543(92)90048-W. PMID 1354645.
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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By group |
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SLC1–10 |
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(1): | |
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(2): | |
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(3): | |
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(4): | |
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(5): | |
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(6): | |
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(7): | |
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(8): | |
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(9): | |
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(10): | |
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| SLC11–20 |
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(11): |
- proton coupled metal ion transporter
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(12): | |
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(13): |
- human Na+-sulfate/carboxylate cotransporter
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(14): | |
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(15): |
- proton oligopeptide cotransporter
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(16): |
- monocarboxylate transporter
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(17): | |
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(18): | |
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(19): | |
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(20): | |
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| SLC21–30 |
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(21): | |
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(22): | |
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(23): |
- Na+-dependent ascorbic acid transporter
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(24): | |
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(25): | |
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(26): |
- multifunctional anion exchanger
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(27): | |
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(28): |
- Na+-coupled nucleoside transport (SLC28A1
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(29): |
- facilitative nucleoside transporter
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(30): | |
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| SLC31–40 |
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(31): | |
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(32): | |
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(33): | |
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(34): |
- type II Na+-phosphate cotransporter
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(35): |
- nucleoside-sugar transporter
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-
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- SLC35E1
- SLC35E2
- SLC35E3
- SLC35E4
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(36): | |
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(37): |
- sugar-phosphate/phosphate exchanger
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(38): |
- System A & N, sodium-coupled neutral amino-acid transporter
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(39): | |
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(40): |
- basolateral iron transporter
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| SLC41–48 |
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(41): | |
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(42): | |
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(43): |
- Na+-independent, system-L like amino-acid transporter
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(44): | |
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(45): |
- Putative sugar transporter
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(46): | |
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(47): | |
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(48): | |
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see also solute carrier disorders |