SLC35C1

Description		solute carrier family 35 member C1
Image		No pdb structure
GO Annotations	Cellular Component	Golgi Membrane Golgi Apparatus Integral Component Of Membrane
	Molecular Function	GDP-fucose Transmembrane Transporter Activity Antiporter Activity
	Biological Process	Carbohydrate Transport Lipid Glycosylation Protein O-linked Fucosylation GDP-fucose Import Into Golgi Lumen Negative Regulation Of Notch Signaling Pathway
Pathways		Defective SLC35C1 causes congenital disorder of glycosylation 2C (CDG2C) GDP-fucose biosynthesis Transport of nucleotide sugars
Drugs
Diseases		Congenital disorders of glycosylation (CDG) type II Leukocyte adhesion deficiency (LAD), including the following four diseases: Leukocyte adhesion deficiency (I); Leukocyte adhesion deficiency (II); Leukocyte adhesion deficiency (III); LAD with Rac2 deficiency
GWAS		Axial length ( 24144296) Diastolic blood pressure ( 26969751) Visceral fat ( 22589738)
Novel Interacting Genes		1 novel interacting genes: AMBRA1
Interacting Genes
Entrez ID		55343
HPRD ID		09324
Ensembl ID		ENSG00000181830
Uniprot IDs		B3KQH0 Q96A29
PDB IDs
Enriched GO Terms of Interacting Partners?
Tagcloud ?