Full Name: Solute Carrier Family 6 Member 8
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.
Synonyms: CCDS1; CRT; CRTR; CT1; CTR5
Research Areas: Signal Transduction
Pathways: Signal Transduction Pathway
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