Ontify
⌘
S
⌘
S
Share
Defective SLC35A1 Causes Congenital Disorder of Glycosylation 2F (CDG2F)
Instance of the biological pathway in Homo sapiens with Reactome ID (R-HSA-5663020).
Statements about
Defective SLC35A1 Causes Congenital Disorder of Glycosylation 2F (CDG2F)
Part Of
SLC Transporter Disorders
Has Part(s)
Defective SLC35A1 Does Not Exchange CMP-Neu5Ac for CMP
Exact Match
https://identifiers.org/reactome:R-H ...
Instance Of
Biological Pathway
