SLC22A25

(Redirected from SLC22A19)

Solute carrier family 22 member 25 (SLC22A25), also known as organic anion transporter UST6, is a protein that in humans is encoded by the SLC22A25 gene.[5][6]

SLC22A25
Identifiers
AliasesSLC22A25, HIMTP, UST6, solute carrier family 22 member 25
External IDsOMIM: 610792; MGI: 2442750; HomoloGene: 77136; GeneCards: SLC22A25; OMA:SLC22A25 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_199352
NM_001394058
NM_001394059

NM_177002

RefSeq (protein)

NP_955384

n/a

Location (UCSC)Chr 11: 63.16 – 63.24 MbChr 19: 8.31 – 8.38 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000196600Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000052562Ensembl, 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. ^ "Entrez Gene: solute carrier family 22".
  6. ^ Jacobsson JA; Haitina T; Lindblom J; Fredriksson R (November 2007). "Identification of six putative human transporters with structural similarity to the drug transporter SLC22 family". Genomics. 90 (5): 595–609. doi:10.1016/j.ygeno.2007.03.017. PMID 17714910.

Further reading

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This article incorporates text from the United States National Library of Medicine, which is in the public domain.