SLC22A25

SLC22A25
Identifiers
Aliases	SLC22A25, HIMTP, UST6, solute carrier family 22 member 25
External IDs	MGI: 2442750 HomoloGene: 77136 GeneCards: SLC22A25
Gene location (Human)
Chr.	Chromosome 11 (human)[1]
End	63,229,652 bp[1]
Gene location (Mouse)
Chr.	Chromosome 19 (mouse)[2]
End	8,405,111 bp[2]
Gene ontology
Molecular function	• sodium-independent organic anion transmembrane transporter activity; • inorganic anion exchanger activity; • urate transmembrane transporter activity;
Cellular component	• integral component of membrane; • integral component of plasma membrane; • membrane;
Biological process	• sodium-independent organic anion transport; • transmembrane transport; • inorganic anion transport; • urate transport;
	Sources:Amigo / QuickGO
Orthologs
	387601
	319800
	ENSG00000196600
	ENSMUSG00000052562
	Q6T423
	n/a
	NM_199352
	NM_177002
	NP_955384
	n/a
	Wikidata
View/Edit Human	View/Edit Mouse

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]

References

1 2 3 GRCh38: Ensembl release 89: ENSG00000196600 - Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000052562 - Ensembl, May 2017
↑ "Human PubMed Reference:".
↑ "Mouse PubMed Reference:".
↑ "Entrez Gene: solute carrier family 22".
↑ 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.

Eraly SA; Monte JC; Nigam SK (2004). "Novel slc22 transporter homologs in fly, worm, and human clarify the phylogeny of organic anion and cation transporters". Physiol. Genomics. 18 (1): 12–24. doi:10.1152/physiolgenomics.00014.2004. PMID 15054140.
Strausberg RL, Feingold EA, Grouse LH, et al. (2002). "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. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
Zaïr ZM; Eloranta JJ; Stieger B; Kullak-Ublick GA (2008). "Pharmacogenetics of OATP (SLC21/SLCO), OAT and OCT (SLC22) and PEPT (SLC15) transporters in the intestine, liver and kidney". Pharmacogenomics. 9 (5): 597–624. doi:10.2217/14622416.9.5.597. PMID 18466105.
Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.

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

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[refGRCh38Ensembl-1] 1 2 3 GRCh38: Ensembl release 89: ENSG00000196600 - Ensembl, May 2017

[refGRCm38Ensembl-2] 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000052562 - Ensembl, May 2017

[3] "Human PubMed Reference:".

[4] "Mouse PubMed Reference:".

[entrez-5] "Entrez Gene: solute carrier family 22".

[pmid17714910-6] 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.

SLC22A25

References

Further reading