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English
Defective B4GALT1 does not transfer Gal to the keratan chain
An instance of the biological reaction in Homo sapiens with Reactome ID (R-HSA-3656230)
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Statements
instance of
biological process
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-3656230
part of
Defective B4GALT1 causes B4GALT1-CDG (CDG-2d)
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-3656230
found in taxon
Homo sapiens
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-3656230
exact match
https://identifiers.org/reactome:R-HSA-3656230
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-3656230
has part(s)
Keratan(1)-PG [Golgi lumen]
quantity
1
object has role
reactant
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-3656230
B4GALT1 R345Kfs*6 [Golgi membrane]
quantity
1
object has role
modifier
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-3656230
UDP-D-galactose(2-)
quantity
1
object has role
reactant
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-3656230
cites work
Deficiency of UDP-galactose:N-acetylglucosamine beta-1,4-galactosyltransferase I causes the congenital disorder of glycosylation type IId.
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-3656230
Identifiers
Reactome ID
R-HSA-3656230
1 reference
stated in
Reactome
retrieved
8 July 2022
Reactome ID
R-HSA-3656230
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