Reactome: A Curated Pathway Database
THIS SITE IS USED FOR CURATION AND TESTING
IT IS NOT STABLE, IS LINKED TO AN INCOMPLETE DATA SET, AND IS NOT MONITORED FOR PERFORMANCE. WE STRONGLY RECOMMEND THE USE OF OUR PUBLIC SITE

Query author contributions in Reactome

Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.

If you have an ORCID ID that is not listed on this page, please forward this information to us and we will update your Reactome pathway records.

Name Email address

Details on Person The human gene SLC35C1 encodes a GDP-fucose transporter that...

Class:IdSummation:5653591
_displayNameThe human gene SLC35C1 encodes a GDP-fucose transporter that...
_timestamp2023-06-23 14:16:05
created[InstanceEdit:5653590] Jassal, Bijay, 2014-12-01
modified[InstanceEdit:9838639] D'Eustachio, Peter, 2023-06-23
textThe human gene SLC35C1 encodes a GDP-fucose transporter that resides on the Golgi membrane and mediates the transport of GDP-fucose into the Golgi lumen. Defects in SLC35C1 cause the congenital disorder of glycosylation type 2C (CDG2C aka leukocyte adhesion deficiency type II, LAD2), an autosomal recessive disorder characterised by moderate to severe psychomotor retardation, mild dysmorphism and impaired neutrophil motility. Mutations causing CDG2C are R147C, T308*, E31* and F168del (Lubke et al. 2001, Dauber et al. 2014).
(summation)[FailedReaction:5653596] Defective SLC35C1 does not transport UDP-Fuc from cytosol to Golgi lumen [Homo sapiens]
[Change default viewing format]
No pathways have been reviewed or authored by The human gene SLC35C1 encodes a GDP-fucose transporter that... (5653591)