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ProteomicsLFQP of lysates from wild-type and TBC1D20-null HeLa cells
These data are from two wild-type HeLa clones (WT1, WT2) and two TBC1D20-null clones (5H2, 7H5), each analysed in triplicate.
ORGANISM(S): Homo sapiens (Human) 
2024-01-26 | PXD016233 | Pride
Human Hela Rab18 Tbc1d20 Lfqp. 
UnknownTBC1D20 mediates autophagy as a key regulator of autophagosome maturation.
Not available
S-EPMC5079675 | biostudies-literature
UnknownTBC1D20 coordinates vesicle transport and actin remodeling to regulate ciliogenesis.
Not available
S-EPMC11781271 | biostudies-literature
ProteomicsLFQP of lysates from wild-type, RAB18-, TBC1D20-, RAB3GAP1- and RAB3GAP2-null RPE1 cells
These data are from two wild-type RPE1 clones (WT11, WT20), a RAB18-null clone, a TBC1D20-null clone, a RAB3GAP1-null clone and a RAB3GAP2-null clone, each analysed in triplicate.
ORGANISM(S): Homo sapiens (Human) 
2024-01-26 | PXD016326 | Pride
Human Rpe1 Rab18 Rab3gap1 Tbc1d20 Lfqp Rab3gap2 
UnknownLoss-of-function mutations in TBC1D20 cause cataracts and male infertility in blind sterile mice and Warburg micro syndrome in humans.
Not available
S-EPMC3852926 | biostudies-literature
UnknownRole for TBC1D20 and Rab1 in hepatitis C virus replication via interaction with lipid droplet-bound nonstructural protein 5A.
Not available
S-EPMC3393552 | biostudies-literature
UnknownWarburg Micro syndrome is caused by RAB18 deficiency or dysregulation.
Not available
S-EPMC4632505 | biostudies-literature
UnknownTwo novel homozygous RAB3GAP1 mutations cause Warburg micro syndrome.
Not available
S-EPMC4785564 | biostudies-literature
UnknownTDRD7 participates in lens development and spermiogenesis by mediating autophagosome maturation.
Not available
S-EPMC8632297 | biostudies-literature
UnknownLarge homozygous RAB3GAP1 gene microdeletion causes Warburg micro syndrome 1.
Not available
S-EPMC4224754 | biostudies-literature
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