FAQ

ALG9 gene

Known as: DISRUPTED IN BIPOLAR DISORDER 1, ALG9, S. CEREVISIAE, HOMOLOG OF, ALG9, alpha-1,2-mannosyltransferase 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1996-2016
02419962016

Related topics

Related topics

1 relation
ALG1 gene

Related mentions per year

Related mentions per year

1984-2018
19801990200020102020
ALG9 gene
ALG1 gene

Papers overview

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2016
2016
Further Delineation of the ALG9-CDG Phenotype.
ALG9-CDG is one of the less frequently reported types of CDG. Here, we summarize the features of six patients with ALG9-CDG… (More)
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2016
2016
A novel phenotype in N-glycosylation disorders: Gillessen-Kaesbach–Nishimura skeletal dysplasia due to pathogenic variants in ALG9
A rare lethal autosomal recessive syndrome with skeletal dysplasia, polycystic kidneys and multiple malformations was first… (More)
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2010
2010
Microarray analysis of relative gene expression stability for selection of internal reference genes in the rhesus macaque brain
Normalization of gene expression data refers to the comparison of expression values using reference standards that are consistent… (More)
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Highly Cited
2009
Highly Cited
2009
Validation of reference genes for quantitative expression analysis by real-time RT-PCR in Saccharomyces cerevisiae
Real-time RT-PCR is the recommended method for quantitative gene expression analysis. A compulsory step is the selection of good… (More)
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2009
2009
Quality control of glycoproteins bearing truncated glycans in an ALG9-defective (CDG-IL) patient.
We describe an ALG9-defective (congenital disorders of glycosylation type IL) patient who is homozygous for the p.Y286C (c.860A>G… (More)
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2009
2009
Predicting neuroendocrine tumor (carcinoid) neoplasia using gene expression profiling and supervised machine learning.
BACKGROUND A more accurate taxonomy of small intestinal (SI) neuroendocrine tumors (NETs) is necessary to accurately predict… (More)
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2005
2005
CDG-IL: an infant with a novel mutation in the ALG9 gene and additional phenotypic features.
We describe the second case of congenital disorder of glycosylation type IL (CDG-IL) caused by deficiency of the ALG9 a1,2… (More)
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2005
2005
ALG9 mannosyltransferase is involved in two different steps of lipid-linked oligosaccharide biosynthesis.
N-linked protein glycosylation follows a conserved pathway in eukaryotic cells. The assembly of the lipid-linked core… (More)
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2004
2004
Identification and functional analysis of a defect in the human ALG9 gene: definition of congenital disorder of glycosylation type IL.
Defects of lipid-linked oligosaccharide assembly lead to alterations of N-linked glycosylation known as "type I congenital… (More)
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1996
1996
Stepwise assembly of the lipid-linked oligosaccharide in the endoplasmic reticulum of Saccharomyces cerevisiae: identification of the ALG9 gene encoding a putative mannosyl transferase.
The core oligosaccharide Glc3Man9GlcNAc2 is assembled at the membrane of the endoplasmic reticulum on the lipid carrier dolichyl… (More)
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