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(Q50296247)
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English
ALG9 transfers Man to N-glycan precursor (GlcNAc)2 (Man)6 (PP-Dol)1
An instance of the biological reaction in Homo sapiens with Reactome ID (R-HSA-446215)
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Statements
instance of
biological process
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-446215
part of
Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-446215
found in taxon
Homo sapiens
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-446215
exact match
https://identifiers.org/reactome:R-HSA-446215
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-446215
has part(s)
ALG9 alpha-1,2-mannosyltransferase
quantity
1
object has role
modifier
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-446215
Mannose-P-dolichol utilization defect 1
quantity
1
object has role
modifier
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-446215
cites work
Common variations in ALG9 are not associated with bipolar I disorder: a family-based study
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-446215
Identification and functional analysis of a defect in the human ALG9 gene: definition of congenital disorder of glycosylation type IL.
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-446215
A mannosyltransferase gene at 11q23 is disrupted by a translocation breakpoint that co-segregates with bipolar affective disorder in a small family
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-446215
CDG-IL: an infant with a novel mutation in the ALG9 gene and additional phenotypic features.
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-446215
Identifiers
Reactome ID
R-HSA-446215
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-446215
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