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Defective SLC35C1 Causes Congenital Disorder of Glycosylation 2C (CDG2C) - Ontify
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Defective SLC35C1 Causes Congenital Disorder of Glycosylation 2C (CDG2C)
Instance of the biological pathway in Homo sapiens with Reactome ID (R-HSA-5619078).
Statements about
Defective SLC35C1 Causes Congenital Disorder of Glycosylation 2C (CDG2C)
Part Of
SLC Transporter Disorders
Instance Of
Biological Pathway
Has Part(s)
Defective SLC35C1 Does Not Transport UDP-Fuc From Cytosol to Golgi Lumen
Exact Match
https://identifiers.org/reactome:R-H ...
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