Presku: | APL00006 |
Size: | 200ug |
Weight: | 14kDa |
Gene: | 23710 |
Target: | GPD1L belongs to the NAD-dependent glycerol-3-phosphate dehydrogenase family. Defects in GPD1L are the cause of Brugada syndrome type 2 (BRS2) and sudden infant death syndrome (SIDS). |
Alternative names: | APG8L; ATG8; ATG8L; GEC1; ATG8B; APG8-LIKE |