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ProteomicsFunctional assays of human ALG9
Asparagine-linked glycans are essential for the maturation and function of most eukaryotic secretory proteins. Biosynthesis and transfer of the GlcNAc2Man9Glc3 glycan occurs on the endoplasmic reticulum (ER) membrane, in a highly conserved process involving more than a dozen membrane proteins whose ...
ORGANISM(S): synthetic construct 
2026-05-30 | PXD072144 | Pride
Alg9 Oligomannose N-glycans 
UnknownHeterozygosity of ALG9 in Association with Autosomal Dominant Polycystic Liver Disease.
Not available
S-EPMC10530326 | biostudies-literature
UnknownALG9 Mutation Carriers Develop Kidney and Liver Cysts.
Not available
S-EPMC6830805 | biostudies-literature
UnknownCommon variations in ALG9 are not associated with bipolar I disorder: a family-based study.
Not available
S-EPMC1569366 | biostudies-literature
UnknownIdentification and functional analysis of a defect in the human ALG9 gene: definition of congenital disorder of glycosylation type IL.
Not available
S-EPMC1181998 | biostudies-literature
UnknownA novel phenotype in N-glycosylation disorders: Gillessen-Kaesbach-Nishimura skeletal dysplasia due to pathogenic variants in ALG9.
Not available
S-EPMC4717212 | biostudies-literature
UnknownMass spectrometric analysis of neutral and anionic N-glycans from a Dictyostelium discoideum model for human congenital disorder of glycosylation CDG IL.
Not available
S-EPMC3588589 | biostudies-literature
UnknownSynergistic use of glycomics and single-molecule molecular inversion probes for identification of congenital disorders of glycosylation type-1.
Not available
S-EPMC9545396 | biostudies-literature
UnknownIdentify Functional lncRNAs in Nonalcoholic Fatty Liver Disease by Constructing a ceRNA Network.
Not available
S-EPMC9260751 | biostudies-literature
UnknownSkeletal and Bone Mineral Density Features, Genetic Profile in Congenital Disorders of Glycosylation: Review.
Not available
S-EPMC8391432 | biostudies-literature
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