SLC22A11

Source: Wikipedia, the free encyclopedia.
SLC22A11
Identifiers
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo / QuickGO
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

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

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

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000168065Ensembl, May 2017
  2. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. PMID 10660625
    .
  4. .
  5. .
  6. ^ a b "Entrez Gene: SLC22A11 solute carrier family 22 (organic anion/cation transporter), member 11".

Further reading

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