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SLC13A5

Official Full Name
solute carrier family 13 member 5
Organism
Homo sapiens
GeneID
284111
Background
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
INDY; NACT; DEE25; mIndy; EIEE25;

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