GlyCosmos Portal

GlyCosmos Glycogenes

Integrated list of glycan-related genes, including glycosyltransferases, hydrolases, etc. Gene Symbol Aliases include gene descriptions and names of orthologs.

Database	Last Updated
FlyGlycoDB	March 25, 2024
Glyco-Disease Genes Database (GDGDB)	January 25, 2017
GlycoGene Database (GGDB)	January 26, 2018
KEGG BRITE	September 20, 2023
LIPID MAPSGene/Proteome Database	June 24, 2019
Plant GARDEN	May 28, 2020
UniProt	August 23, 2023
Human Phenotype Ontology	July 12, 2023

Gene Symbol	Gene Symbol Aliases	Gene ID	Disease Name ▼	Species
RFT1	CDG1N congenital disorder of glycosylation 1N	91869	RFT1-CDG	Homo sapiens
GAA	Pompe disease glycogen storage disease type II	2548	Pompe disease Pompe disease, infantile-onset form Pompe disease, late-onset form	Homo sapiens
PIGA	GPI3 GPI3 (SPT14) homolog (S. cerevisiae) PIG-A Phosphatidylinositol N-acetylglucosaminyltransferase subunit A paroxysmal nocturnal hemoglobinuria	5277	Paroxysmal nocturnal hemoglobinuria, somatic (SOMATIC MUTATION)	Homo sapiens
POMGNT1	FLJ20277 LGMD2O MGAT1.2 protein O-mannose beta-1,2-N-acetylglucosaminyltransferase	55624	POMGNT1-CDG (cong. muscular dystrophy spectrum)	Homo sapiens
PMM2	CDG1a CDGS Congenital disorder of glycosylation, type Ia PMI PMI1 mannose-6-phosphate isomerase phosphomannose isomerase 1	5373	PMM2-CDG PMM2-CDG, adult stable disability stage PMM2-CDG, infantile multisystem stage PMM2-CDG, late-infantile and childhood ataxia-intellectual disability stage	Homo sapiens
PIGM	DPM:GlcN-(acyl-)PI mannosyltransferase GPI mannosyltransferase 1 GPI-MT-I PIG-M dol-P-Man dependent GPI mannosyltransferase	93183	PIGM-CDG	Homo sapiens
PGM1		5236	PGM1-CDG	Homo sapiens
SMPD1	ASM Niemann-Pick type A/B acid sphingomyelinase	6609	Niemann-Pick disease, type A Niemann-Pick disease, type B	Homo sapiens
GFPT1	GFA GFAT GFAT1	2673	Myasthenia, congenital, with tubular aggregates 1	Homo sapiens
FKRP	FKTR LGMD2I MDC1C	79147	Muscular dystrophy, congenital, type 1C Muscular dystrophy, limb-girdle, type 2I	Homo sapiens