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SLC25A22 encodes a mitochondrial glutamate carrier. Additionally we are shipping SLC25A22 Antibodies (8) and SLC25A22 Proteins (3) and many more products for this protein.
SLC25A22 is responsible for migrating partial seizures in infancy, demonstrated by combining linkage analysis and whole exome sequencing.
Compares and contrasts all the known human SLC25A (show SLC25A25 ELISA Kits)* genes and includes functional information.
A novel SLC25A22 mutation in an unrelated patient born from first cousin Algerian parents and presenting severe epileptic encephalopathy, is described.
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.
glutamate/H(+) symporter 1
, mitochondrial glutamate carrier 1
, solute carrier family 25 member 22
, solute carrier family 25 (mitochondrial carrier, glutamate), member 22