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GlyCosmos Genes

Integrated list of glycan-related genes extracted KEGG GENES Database, UniProt, GlycoGene Database (GGDB), Plant GARDEN and FlyGlycoDB. Glycan-related genes including glycosyltransferase, hydrolase activity (acting on glycosyl bonds), carbohydrate metabolic process, etc .

Source	Last Updated
FlyGlycoDB	March 25, 2024
GlycoGene Database (GGDB)	January 26, 2018
KEGG GENES Database	September 20, 2023
Plant GARDEN	May 28, 2020
UniProt	July 8, 2024

Selecting the function you want to look up from the categories displays a list narrowed down to glycan-related genes with that function (Gene Ontology).

Catalytic activity

glycosyltransferase activity

hydrolase activity, acting on glycosyl bonds

Binding

carbohydrate binding

Response to carbohydrate

Primary metabolic process

Displaying entries **151 - 175** of **186** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
174705	Zinc finger transcription factor pqm-1	pqm-1	Caenorhabditis elegans
174633	Alpha-1,2-mannosyltransferase algn-9	algn-9	Caenorhabditis elegans	congenital disorder of glycosylation Il congenital disorder of glycosylation type I
174603	Glyceraldehyde-3-phosphate dehydrogenase 1	gpd-1	Caenorhabditis elegans	Alzheimer's disease brain glioma diabetic retinopathy epilepsy lymphangioleiomyomatosis middle cerebral artery infarction obesity oral squamous cell carcinoma rheumatic heart disease
174578	Glyceraldehyde-3-phosphate dehydrogenase 4	gpd-4	Caenorhabditis elegans	Alzheimer's disease brain glioma diabetic retinopathy epilepsy lymphangioleiomyomatosis middle cerebral artery infarction obesity oral squamous cell carcinoma rheumatic heart disease
174542	putative dolichyl pyrophosphate Glc1Man9GlcNAc2 alpha-1,3-glucosyltransferase	algn-8	Caenorhabditis elegans	congenital disorder of glycosylation Ih congenital disorder of glycosylation type I polycystic liver disease
174517	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase sqv-8	sqv-8	Caenorhabditis elegans	Barrett's esophagus Larsen-like syndrome B3GAT3 type pulmonary fibrosis schizophrenia
174507	Putative UDP-glucuronosyltransferase ugt-58	ugt-58	Caenorhabditis elegans
174423	Enolase	enol-1	Caenorhabditis elegans	Alzheimer's disease Parkinsonism aortic valve stenosis brain disease breast carcinoma hypertension migraine without aura neuroendocrine carcinoma prostate cancer toxic shock syndrome urinary bladder cancer visual epilepsy
174386	phosphatidylinositol N-acetylglucosaminyltransferase	piga-1	Caenorhabditis elegans	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
174243	Uncharacterized protein	B0495.5	Caenorhabditis elegans	oligoasthenoteratozoospermia
174145	UDP-sugar transporter sqv-7	sqv-7	Caenorhabditis elegans	schneckenbecken dysplasia
174131	Sphingomyelin phosphodiesterase 1	asm-1	Caenorhabditis elegans	Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease Wilson disease
174001	Ceramide glucosyltransferase 3	cgt-3	Caenorhabditis elegans	hypertension
173958	Alpha-(1,3)-fucosyltransferase fut-3	fut-3	Caenorhabditis elegans
173912	Alpha-1,3/1,6-mannosyltransferase ALG2	algn-2	Caenorhabditis elegans	congenital disorder of glycosylation Ii congenital myasthenic syndrome 14
173911	Putative deoxyribose-phosphate aldolase	F09E5.3	Caenorhabditis elegans
173747	putative glycerol kinase	R11F4.1	Caenorhabditis elegans	familial hypercholesterolemia glycerol kinase deficiency
173635	Beta-1,3-galactosyltransferase sqv-2	sqv-2	Caenorhabditis elegans	Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome spondyloepimetaphyseal dysplasia with joint laxity type 1
173574	Putative glucosylceramidase 1	gba-1	Caenorhabditis elegans	Gaucher's disease type I Gaucher's disease type II Gaucher's disease Lewy body dementia Parkinson's disease
173469	Fukutin;Nucleotidyltransferase family protein	T07D3.4	Caenorhabditis elegans	Fukuyama congenital muscular dystrophy Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M dilated cardiomyopathy 1B dilated cardiomyopathy 1X muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B4 muscular dystrophy
173405	Chitin synthase chs-2;chitin synthase	chs-2	Caenorhabditis elegans
173393	putative ADP-dependent glucokinase	C50D2.7	Caenorhabditis elegans
173171	UDP-glucose 4-epimerase	gale-1	Caenorhabditis elegans	galactose epimerase deficiency galactosemia thrombocytopenia
173114	Beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 3	gly-15	Caenorhabditis elegans	cataract 13 with adult i phenotype cataract
173109	GLYcosylation related	gly-16	Caenorhabditis elegans	cataract 13 with adult i phenotype cataract

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