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Defective SLC35A2 Causes Congenital Disorder of Glycosylation 2M (CDG2M) - Ontify
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Defective SLC35A2 Causes Congenital Disorder of Glycosylation 2M (CDG2M)
Instance of the biological pathway in Homo sapiens with Reactome ID (R-HSA-5619072).
Statements about
Defective SLC35A2 Causes Congenital Disorder of Glycosylation 2M (CDG2M)
Part Of
SLC Transporter Disorders
Instance Of
Biological Pathway
Has Part(s)
Defective SLC35A2 Does Not Exchange UDP-Gal, UDP-GalNAc for UMP
Exact Match
https://identifiers.org/reactome:R-H ...
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