Protein-coding gene in the species Homo sapiens
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 [ edit ] References [ edit ]
^ 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 [ edit ]
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 .
By group
SLC1–10
(1): (2): (3): (4): (5): (6): (7): (8): (9): (10):
SLC11–20
(11): (12): (13): (14): (15): (16): (17): (18): (19): (20):
SLC21–30
(21): (22): (23): (24): (25): (26): (27): (28): (29): (30):
SLC31–40
(31): (32): (33): (34): (35): (36): (37): (38): (39): (40):
SLC41–48
(41): (42): (43): (44): (45): (46): (47): (48):
