SLC13A5, solute carrier family 13 member 5

SLC13A5, solute carrier family 13 member 5

• 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]

• Gene Synonyms (solute carrier family 13 member 5, Na(+)/citrate cotransporter, Na+-coupled citrate transporter protein, sodium-dependent dicarboxylate transporter, solute carrier family 13 (sodium-dependent citrate transporter), member 5, EIEE25, INDY, NACT, mIndy,)
• NCBI Gene ID: 284111
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q86YT5
  UNIPROT ID#>>Q68D44
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

solute carrier family 13 member 5 interacts with:

• cysteine rich tail 1
  keratin associated protein 10-8
  keratin associated protein 11-1
  keratin associated protein 12-2
  keratin associated protein 12-3
  keratin associated protein 5-2

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.