SLC22A11

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Solute carrier family 22 member 11 is a protein that in humans is encoded by the SLC22A11 gene.[3][4][5][6]

AliasesSLC22A11, OAT4, hOAT4, solute carrier family 22 member 11
End64,572,875 bp[1]
Quick facts Identifiers, Aliases ...
SLC22A11
Identifiers
AliasesSLC22A11, OAT4, hOAT4, solute carrier family 22 member 11
External IDsOMIM: 607097; HomoloGene: 81863; GeneCards: SLC22A11; OMA:SLC22A11 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001307985
NM_018484

n/a

RefSeq (protein)

NP_001294914
NP_060954

n/a

Location (UCSC)Chr 11: 64.56 – 64.57 Mbn/a
PubMed search[2]n/a
Wikidata
View/Edit Human
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The protein encoded by this gene is involved in the sodium-independent transport and excretion of organic anions, some of which are potentially toxic. The encoded protein is an integral membrane protein and is found mainly in the kidney and in the placenta, where it may act to prevent potentially harmful organic anions from reaching the fetus.[6]

See also

References

Further reading

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