SLC22A18

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SLC22A18
Identifiers
AliasesSLC22A18, BWR1A, BWSCR1A, HET, IMPT1, ITM, ORCTL2, SLC22A1L, TSSC5, p45-BWR1A, solute carrier family 22 member 18
External IDsOMIM: 602631 MGI: 1336884 HomoloGene: 1918 GeneCards: SLC22A18
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_002555
NM_183233
NM_001315501
NM_001315502

NM_001042760
NM_008767

RefSeq (protein)

NP_001302430
NP_001302431
NP_002546
NP_899056

NP_001036225
NP_032793

Location (UCSC)Chr 11: 2.9 – 2.93 MbChr 7: 143.03 – 143.05 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Solute carrier family 22 member 18 is a protein that in humans is encoded by the SLC22A18 gene.[5][6][7]

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See also

References

  1. ^ a b c ENSG00000110628 GRCh38: Ensembl release 89: ENSG00000276130, ENSG00000110628Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000000154Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ 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.
  6. ^ 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.
  7. ^ "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.

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