Protein Name | solute carrier family 13 member 5 |
---|---|
Organism | Homo sapiens |
Gene ID | 284111 |
Gene Symbol | SLC13A5 |
UniProt | Q86YT5 (S13A5_HUMAN), Q68D44 (Q68D44_HUMAN) |
Relationships |
Total Number of functionally related compound(s) :
79
Total Number of Articles : 78 |
Description |
solute carrier family 13 member 5 |
Gene Summary |
This gene encodes a protein belonging to the solute carrier family 13 group of proteins. This family member is a sodium-dependent citrate cotransporter that may regulate metabolic processes. Mutations in this gene cause early infantile epileptic encephalopathy 25. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2014] |
synonyms |
|
Properties | |