SLC22A10

Protein-coding gene in the species Homo sapiens
SLC22A10
Identifiers
AliasesSLC22A10, OAT5, hOAT5, solute carrier family 22 member 10
External IDsOMIM: 607580 HomoloGene: 111144 GeneCards: SLC22A10
Gene location (Human)
Chromosome 11 (human)
Chr.Chromosome 11 (human)[1]
Chromosome 11 (human)
Genomic location for SLC22A10
Genomic location for SLC22A10
Band11q12.3Start63,268,022 bp[1]
End63,311,783 bp[1]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • liver

  • right lobe of liver

  • superior frontal gyrus

  • Brodmann area 9

  • cingulate gyrus

  • temporal lobe

  • amygdala

  • lung

  • upper lobe of left lung

  • corpus callosum
    n/a
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
  • sodium-independent organic anion transmembrane transporter activity
  • transmembrane transporter activity
  • inorganic anion exchanger activity
  • urate transmembrane transporter activity
Cellular component
  • integral component of membrane
  • integral component of plasma membrane
  • membrane
  • plasma membrane
Biological process
  • sodium-independent organic anion transport
  • transmembrane transport
  • inorganic anion transport
  • urate transport
  • organic anion transport
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

387775

n/a

Ensembl

ENSG00000184999

n/a

UniProt

Q63ZE4

n/a

RefSeq (mRNA)

NM_001039752

n/a

RefSeq (protein)

NP_001034841

n/a

Location (UCSC)Chr 11: 63.27 – 63.31 Mbn/a
PubMed search[2]n/a
Wikidata
View/Edit Human

Solute carrier family 22 member 10 (SLC22A10), also known as organic anion transporter 5 (OAT5), is a protein that in humans is encoded by the SLC22A10 gene.[3][4]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000184999 – Ensembl, May 2017
  2. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. ^ "Entrez Gene: solute carrier family 22".
  4. ^ Sun W; Wu RR; van Poelje PD; Erion MD (May 2001). "Isolation of a family of organic anion transporters from human liver and kidney". Biochem. Biophys. Res. Commun. 283 (2): 417–22. doi:10.1006/bbrc.2001.4774. PMID 11327718.

Further reading

  • Wang AG, Yoon SY, Oh JH, et al. (2006). "Identification of intrahepatic cholangiocarcinoma related genes by comparison with normal liver tissues using expressed sequence tags". Biochem. Biophys. Res. Commun. 345 (3): 1022–32. doi:10.1016/j.bbrc.2006.04.175. PMID 16712791.
  • Eraly SA; Nigam SK (2002). "Novel human cDNAs homologous to Drosophila Orct and mammalian carnitine transporters". Biochem. Biophys. Res. Commun. 297 (5): 1159–66. doi:10.1016/S0006-291X(02)02343-4. PMID 12372408.
  • 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. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
  • Taylor TD, Noguchi H, Totoki Y, et al. (2006). "Human chromosome 11 DNA sequence and analysis including novel gene identification". Nature. 440 (7083): 497–500. Bibcode:2006Natur.440..497T. doi:10.1038/nature04632. PMID 16554811.

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

  • v
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By group
SLC1–10
(1):
(2):
(3):
(4):
(5):
(6):
(7):
(8):
  • Na+/Ca2+ exchanger
(9):
(10):
SLC11–20
(11):
(12):
(13):
(14):
(15):
(16):
(17):
(18):
(19):
(20):
SLC21–30
(21):
(22):
(23):
  • Na+-dependent ascorbic acid transporter
(24):
  • Na+/(Ca2+-K+) exchanger
(25):
(26):
(27):
(28):
(29):
(30):
SLC31–40
(31):
(32):
(33):
(34):
(35):
(36):
(37):
(38):
(39):
(40):
  • basolateral iron transporter
SLC41–48
(41):
(42):
(43):
  • Na+-independent, system-L like amino-acid transporter
(44):
(45):
(46):
(47):
(48):
SLCO1–4
Symporter, Cotransporter
  • Na+/K+,Cl
  • Na+/Pi3
  • Na+/Cl
  • Na+/glucose
  • Na+/I
  • Cl/K+
Antiporter (exchanger)
  • Na+/H+
  • Na+/Ca2+
    • Na+/(Ca2+-K+) - Cl/HCO
      3
      (Band 3)
  • Cl-formate
  • Cl-oxalate
see also solute carrier disorders


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