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SLC6A8

Official Full Name
solute carrier family 6 member 8
Organism
Homo sapiens
GeneID
6535
Background
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]
Synonyms
CRT; CT1; CRT1; CRTR; CTR5; CCDS1; CRT-1;

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