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ALG9 gene

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

Related topics

Related topics

1 relation
ALG1 gene

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
ALG9 Mutation Carriers Develop Kidney and Liver Cysts.
BACKGROUND Mutations in PKD1 or PKD2 cause typical autosomal dominant polycystic kidney disease (ADPKD), the most common… Expand
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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… Expand
2014
2014
Gut neuroendocrine tumor blood qPCR fingerprint assay: characteristics and reproducibility
Abstract Background: We have developed a PCR-based tool that measures a 51-gene panel for identification of… Expand
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Highly Cited
2007
Highly Cited
2007
GeneChip, geNorm, and gastrointestinal tumors: novel reference genes for real-time PCR.
Accurate quantitation of target genes depends on correct normalization. Use of genes with variable tissue transcription (GAPDH… Expand
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2006
2006
Common variations in ALG9 are not associated with bipolar I disorder: a family-based study
BackgroundA mannosyltransferase gene (ALG9, DIBD1) at chromosome band 11q23 was previously identified to be disrupted by a… Expand
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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… Expand
Highly Cited
2005
Highly Cited
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… Expand
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Highly Cited
2004
Highly Cited
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… Expand
2001
2001
A mannosyltransferase gene at 11q23 is disrupted by a translocation breakpoint that co-segregates with bipolar affective disorder in a small family
Bipolar affective disorder (BPAD) is a complex neuropsychiatric disease characterized by extreme mood swings. Genetic influences… Expand
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Highly Cited
1996
Highly Cited
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… Expand
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