Your search for "c19orf12" returned 80 TaqMan® SNP Genotyping Assays
chromosome 19 open reading frame 12
This gene encodes a small transmembrane protein. Mutations in this gene are a cause of neurodegeneration with brain iron accumulation-4 (NBIA4), but the specific function of the encoded protein is unknown. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]
Please enter the information below and press OK to send your cart to Core Services for purchase.