Your search for "slc25a22" returned 382 TaqMan® SNP Genotyping Assays
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]
1300006L01RIK, AI060884, EIEE3, GC-1, GC1, NET44, RGD1307826, SLC25A22
Please enter the information below and press OK to send your cart to Core Services for purchase.