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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. Protein function: H(+)-myo-inositol cotransporter (PubMed:11500374). Can also transport related stereoisomers (PubMed:11500374). [The UniProt Consortium]
Keywords:
Anti-Hmit, Anti-H(+)-myo-inositol symporter, Anti-H(+)-myo-inositol cotransporter, Anti-Proton myo-inositol cotransporter, Anti-Solute carrier family 2 member 13, SLC2A13 Polyclonal Antibody
This website uses cookies, which are necessary for the technical operation of the website and are always set. Other cookies, which increase the usability of this website, serve for direct advertising or simplify interaction with other websites and social networks, will only be used with your consent.
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