SLC22A18: Difference between revisions
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'''Solute carrier family 22 member 18''' is a [[protein]] that in humans is encoded by the ''SLC22A18'' [[gene]].<ref name="pmid9499412">{{cite journal | author = Dao D, Frank D, Qian N, O'Keefe D, Vosatka RJ, Walsh CP, Tycko B | title = IMPT1, an imprinted gene similar to polyspecific transporter and multi-drug resistance genes | journal = Hum Mol Genet | volume = 7 | issue = 4 | pages = 597–608 |date=May 1998 | pmid = 9499412 | pmc = | doi =10.1093/hmg/7.4.597 }}</ref><ref name="pmid9520460">{{cite journal | author = Schwienbacher C, Sabbioni S, Campi M, Veronese A, Bernardi G, Menegatti A, Hatada I, Mukai T, Ohashi H, Barbanti-Brodano G, Croce CM, Negrini M | title = Transcriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samples | journal = Proc Natl Acad Sci U S A | volume = 95 | issue = 7 | pages = 3873–8 |date=May 1998 | pmid = 9520460 | pmc = 19930 | doi =10.1073/pnas.95.7.3873 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: SLC22A18 solute carrier family 22 (organic cation transporter), member 18| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=5002| accessdate = }}</ref> |
'''Solute carrier family 22 member 18''' is a [[protein]] that in humans is encoded by the ''SLC22A18'' [[gene]].<ref name="pmid9499412">{{cite journal | author = Dao D, Frank D, Qian N, O'Keefe D, Vosatka RJ, Walsh CP, Tycko B | title = IMPT1, an imprinted gene similar to polyspecific transporter and multi-drug resistance genes | journal = Hum Mol Genet | volume = 7 | issue = 4 | pages = 597–608 |date=May 1998 | pmid = 9499412 | pmc = | doi =10.1093/hmg/7.4.597 }}</ref><ref name="pmid9520460">{{cite journal | author = Schwienbacher C, Sabbioni S, Campi M, Veronese A, Bernardi G, Menegatti A, Hatada I, Mukai T, Ohashi H, Barbanti-Brodano G, Croce CM, Negrini M | title = Transcriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samples | journal = Proc Natl Acad Sci U S A | volume = 95 | issue = 7 | pages = 3873–8 |date=May 1998 | pmid = 9520460 | pmc = 19930 | doi =10.1073/pnas.95.7.3873 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: SLC22A18 solute carrier family 22 (organic cation transporter), member 18| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=5002| accessdate = }}</ref> |
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Revision as of 14:06, 20 May 2016
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Identifiers | |||||||||||||||||||||||||||||||||||||||||||||||||||
Aliases | SLC22A18, BWR1A, BWSCR1A, HET, IMPT1, ITM, ORCTL2, SLC22A1L, TSSC5, p45-BWR1A, solute carrier family 22 member 18 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 602631; MGI: 1336884; HomoloGene: 1918; GeneCards: SLC22A18; OMA:SLC22A18 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Solute carrier family 22 member 18 is a protein that in humans is encoded by the SLC22A18 gene.[5][6][7]
See also
References
- ^ a b c ENSG00000110628 GRCh38: Ensembl release 89: ENSG00000276130, ENSG00000110628 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000000154 – 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.
- ^ Dao D, Frank D, Qian N, O'Keefe D, Vosatka RJ, Walsh CP, Tycko B (May 1998). "IMPT1, an imprinted gene similar to polyspecific transporter and multi-drug resistance genes". Hum Mol Genet. 7 (4): 597–608. doi:10.1093/hmg/7.4.597. PMID 9499412.
{{cite journal}}
: CS1 maint: multiple names: authors list (link) - ^ Schwienbacher C, Sabbioni S, Campi M, Veronese A, Bernardi G, Menegatti A, Hatada I, Mukai T, Ohashi H, Barbanti-Brodano G, Croce CM, Negrini M (May 1998). "Transcriptional map of 170-kb region at chromosome 11p15.5: identification and mutational analysis of the BWR1A gene reveals the presence of mutations in tumor samples". Proc Natl Acad Sci U S A. 95 (7): 3873–8. doi:10.1073/pnas.95.7.3873. PMC 19930. PMID 9520460.
{{cite journal}}
: CS1 maint: multiple names: authors list (link) - ^ "Entrez Gene: SLC22A18 solute carrier family 22 (organic cation transporter), member 18".
Further reading
This article incorporates text from the United States National Library of Medicine, which is in the public domain.