Description
Product Characteristics: SLC2A13 (Solute Carrier Family 2 Member 13) is a Protein Coding gene. Diseases associated with SLC2A13 include Arterial Tortuosity Syndrome. Among its related pathways are NRF2 pathway and Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds. Gene Ontology (GO) annotations related to this gene include carbohydrate:proton symporter activity. An important paralog of this gene is SLC2A2.
Target Information: H(+)-myo-inositol cotransporter. Can also transport related stereoisomers