Aliases for SLC5A10 Gene
External Ids for SLC5A10 Gene
Previous GeneCards Identifiers for SLC5A10 Gene
This gene is a member of the sodium/glucose transporter family. Members of this family are sodium-dependent transporters and can be divided into two subfamilies based on sequence homology, one that co-transports sugars and the second that transports molecules such as ascorbate, choline, iodide, lipoate, monocaroboxylates, and pantothenate. The protein encoded by this gene has the highest affinity for mannose and has been reported to be most highly expressed in the kidney. This protein may function as a kidney-specific, sodium-dependent mannose and fructose co-transporter. Alternative splicing results in multiple transcript variants that encode different protein isoforms. [provided by RefSeq, Jul 2012]
GeneCards Summary for SLC5A10 Gene
SLC5A10 (Solute Carrier Family 5 Member 10) is a Protein Coding gene. Diseases associated with SLC5A10 include Benign Familial Infantile Epilepsy. Among its related pathways are Hexose transport and NRF2 pathway. Gene Ontology (GO) annotations related to this gene include transporter activity. An important paralog of this gene is SLC5A9.
UniProtKB/Swiss-Prot Summary for SLC5A10 Gene
High capacity transporter for mannose and fructose and, to a lesser extent, glucose, AMG, and galactose.