Your search for "slc6a8" returned 41 TaqMan® SNP Genotyping Assays
solute carrier family 6 member 8
The protein encoded by this gene is a plasma membrane protein whose function is to transport creatine into and out of cells. Defects in this gene can result in X-linked creatine deficiency syndrome. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]
AA589632, CCDS1, CHOT1, CHT1, CREAT, CRT, CRTR, CT1, CTR5, SLC6A8
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