Aliases for SLC22A8 Gene
External Ids for SLC22A8 Gene
Previous GeneCards Identifiers for SLC22A8 Gene
This gene encodes a protein 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 appears to be localized to the basolateral membrane of the kidney. Multiple alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, May 2010]
GeneCards Summary for SLC22A8 Gene
SLC22A8 (Solute Carrier Family 22 Member 8) is a Protein Coding gene. Diseases associated with SLC22A8 include Gout and Methotrexate Toxicity. Among its related pathways are Blood-Brain Barrier and Immune Cell Transmigration: Pathways Overview and Atenolol Pathway, Pharmacokinetics. Gene Ontology (GO) annotations related to this gene include transmembrane transporter activity and ion transmembrane transporter activity. An important paralog of this gene is SLC22A6.
UniProtKB/Swiss-Prot Summary for SLC22A8 Gene
Plays an important role in the excretion/detoxification of endogenous and exogenous organic anions, especially from the brain and kidney. Involved in the transport basolateral of steviol, fexofenadine. Transports benzylpenicillin (PCG), estrone-3-sulfate (E1S), cimetidine (CMD), 2,4-dichloro-phenoxyacetate (2,4-D), p-amino-hippurate (PAH), acyclovir (ACV) and ochratoxin (OTA).