Aliases for SLC2A10 Gene
External Ids for SLC2A10 Gene
This gene encodes a member of the class III facilitative glucose transporter family. The encoded protein plays a role in regulation of glucose homeostasis. Mutations in this gene have been associated with arterial tortuosity syndrome.[provided by RefSeq, Dec 2009]
GeneCards Summary for SLC2A10 Gene
SLC2A10 (Solute Carrier Family 2 (Facilitated Glucose Transporter), Member 10) is a Protein Coding gene. Diseases associated with SLC2A10 include arterial tortuosity syndrome and loeys-dietz syndrome. Among its related pathways are PAK Pathway and HIF1Alpha Pathway. GO annotations related to this gene include sugar:proton symporter activity. An important paralog of this gene is SLC2A13.
UniProtKB/Swiss-Prot for SLC2A10 Gene
Facilitative glucose transporter