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The enzyme encoded by ALG1 catalyzes the first mannosylation step in the biosynthesis of lipid-linked oligosaccharides. Additionally we are shipping Asparagine-Linked Glycosylation 1, beta-1,4-Mannosyltransferase Homolog (S. Cerevisiae) Antibodies (28) and Asparagine-Linked Glycosylation 1, beta-1,4-Mannosyltransferase Homolog (S. Cerevisiae) Proteins (9) and many more products for this protein.
Study presents molecular, clinical and biochemical findings in the largest collection of ALG1-CDG cases ever reported at a single time with 39 cases, bringing the total number to 57. This ranks it the third most common CDG type behind PMM2 (show PMM2 ELISA Kits)-CDG and ALG6 (show ALG6 ELISA Kits)-CDG. In addition, highly lethal genotype were identified and confirm the presence of a unique xeno-tetrasaccharide in ALG1-CDG patients.
Was detected in the patient's ALG1-coding sequence.
Family study defining the phenotype of deficiency of beta-1,4 mannosyltransferase (MT-1) congenital disorder of glycosylation (CDG), due to ALG1 gene mutations. Four novel ALG1 mutations were identified.
DNA sequencing of ALG1 revealed nine different mutations, seven of which have not been previously reported. Clinical presentations of deficiency are severe, with dysmorphias, CNS involvement and ocular disturbances
The enzyme encoded by this gene catalyzes the first mannosylation step in the biosynthesis of lipid-linked oligosaccharides. This gene is mutated in congenital disorder of glycosylation type Ik.
, GDP-Man:GlcNAc2-PP-dolichol mannosyltransferase
, GDP-mannose-dolichol diphosphochitobiose mannosyltransferase
, asparagine-linked glycosylation 1 homolog (yeast, beta-1,4-mannosyltransferase)
, asparagine-linked glycosylation 1, beta-1,4-mannosyltransferase homolog
, asparagine-linked glycosylation protein 1 homolog
, beta-1,4 mannosyltransferase
, asparagine-linked glycosylation 1 homolog (S. cerevisiae, beta-1,4-mannosyltransferase)
, hypothetical protein