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SLC6A8


Official Full Name
solute carrier family 6 member 8
Organism
Homo sapiens
Gene ID
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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SHH412016 shRNA set against Rat SLC6A8 (NM_017348.2) Inquiry
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CDCH082878 human SLC6A8 ORF clone (NM_001142805.1) Inquiry
CDCH082880 human SLC6A8 ORF clone (NM_001142806.1) Inquiry
CDCH082886 Mouse Slc6a8 ORF clone (NM_001142809.1) Inquiry
CDCH082888 Mouse Slc6a8 ORF clone (NM_001142810.1) Inquiry
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