Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10559
Gene Symbol: SLC35A1
SLC35A1
Congenital disorder of glycosylation type 1q
0.300 Biomarker GENOMICS_ENGLAND Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inactivation of the Golgi CMP-sialic acid transporter. 15576474

2005