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ProteomicsHDX-MS Analysis of the Rab3GAP1/Rab3GAP2
An HDX-MS analysis of the Rab3GAP1 and Rab3GAP2 subunit interface, and the binding interface between Rab18 and the full Rab3GAP1/2 complex.
ORGANISM(S): Homo sapiens (Human) 
2025-03-10 | PXD033072 | Pride
Hdx-ms Rab18 Rab3gap2 Rab3gap1 
GenomicsRAB3GAP2 is a Regulator of Skeletal Muscle Endothelial Cell Proliferation and Associated with Capillary Density
RAB3GAP2 is a Regulator of Skeletal Muscle Endothelial Cell Proliferation and Associated with Capillary Density
PRJNA1390224 | ENA
TranscriptomicsRAB3GAP2 is a Regulator of Skeletal Muscle Endothelial Cell Proliferation and Associated with Capillary Density
Skeletal muscle fiber composition and capillary density influence physical performance and whole-body metabolic properties. ~45% of the variance in fiber type is heritable, which motivated us to perform a genome-wide association study of skeletal muscle histology from 656 Swedish men. Four independe...
ORGANISM(S): Homo sapiens 
2025-12-17 | GSE314190 | GEO
UnknownHypogonadotropic hypogonadism due to variants in RAB3GAP2: expanding the phenotypic and genotypic spectrum of Martsolf syndrome.
Not available
S-EPMC7304352 | 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 
UnknownFOXC1 modulates MYOC secretion through regulation of the exocytic proteins RAB3GAP1, RAB3GAP2 and SNAP25.
Not available
S-EPMC5456087 | biostudies-literature
ProteomicsBioID2(Gly40Ser)-SEC22A proximity biotinylation in HeLa cells
Proximity labelling using transient expression of the same exogenous BioID2(Gly40Ser)-SEC22A construct in wild-type HeLa cells and in otherwise isogenic RAB3GAP1-, RAB3GAP2- and RAB18-null HeLa cell lines.
ORGANISM(S): Homo sapiens (Human) 
2024-01-26 | PXD016404 | Pride
Human Rab3gap2 Sec22a Hela Rab18 Rab3gap1 Bioid Bioid2 
ProteomicsBirA*-RAB18 proximity biotinylation in HeLa cells
Proximity labelling using transient expression of the same exogenous BirA*-RAB18 construct in wild-type HeLa cells and in otherwise isogenic RAB3GAP1-, RAB3GAP2- and TRAPPC9-null HeLa cell lines.
ORGANISM(S): Homo sapiens (Human) 
2024-01-26 | PXD016336 | Pride
Human Bira Hela Bioid 
UnknownMutation in Rab3 GTPase-activating protein (RAB3GAP) noncatalytic subunit in a kindred with Martsolf syndrome.
Not available
S-EPMC1424696 | biostudies-literature
UnknownLoss-of-function mutations in RAB18 cause Warburg micro syndrome.
Not available
S-EPMC3071920 | biostudies-literature
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