SLC25A22, solute carrier family 25 member 22

SLC25A22, solute carrier family 25 member 22

• This gene encodes a mitochondrial glutamate carrier. Mutations in this gene are associated with early infantile epileptic encephalopathy. Multiple alternatively spliced variants, encoding the same protein, have been identified.[provided by RefSeq, Jul 2010]

• Gene Synonyms (mitochondrial glutamate carrier 1, glutamate/H(+) symporter 1, solute carrier family 25 (mitochondrial carrier: glutamate), member 22, EIEE3, GC-1, GC1, NET44,)
• NCBI Gene ID: 79751
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q9H936
• 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 25 member 22 interacts with:

• argonaute RISC component 4
  DNL-type zinc finger
  egl-9 family hypoxia inducible factor 3
  glutamate rich WD repeat containing 1
  integrin alpha FG-GAP repeat containing 1
  solute carrier family 25 member 18
  tubulin, gamma 1

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.