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Background
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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).
Alias Symbols: APG8L, ATG8, ATG8L, GEC1, ATG8B, APG8-LIKE
Protein Interaction Partner: SQSTM1, KRTAP10-3, KRTAP10-9, KRTAP10-7, FAM134C, FUNDC1, ATG4A, AHNAK2, KBTBD7, SCYL3, TNIP1, CALCOCO2, TBC1D5, UBC, SRPK2, SRPK1, DVL2, MAPK15, STBD1, BNIP3L, ULK1, RB1CC1, ATG13, MAP1LC3A, ATG3, ATG4B, ATG7, NBR1, TBC1D16, TBC1D10A, TBC1D17, TBC1D2, TB
Protein Size: 117
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