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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

Search results for "glycoprotein metabolic process"

Displaying entries **151 - 175** of **17827** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
64134	xylosyltransferase 2	Xylt2	Rattus norvegicus (Norway rat)	polycystic kidney disease pseudoxanthoma elasticum
64377	carbohydrate sulfotransferase 8	CHST8 Aliases: GALNAC4ST-1	Homo sapiens (human)	allergic asthma asthma atopic dermatitis colorectal cancer colorectal carcinoma intrinsic asthma large intestine cancer parapsoriasis peeling skin syndrome psoriasis pustulosis of palm and sole scleroderma skin disease systemic scleroderma
64442	ST3 beta-galactoside alpha-2,3-sialyltransferase 2	St3gal2	Rattus norvegicus (Norway rat)
64537	heparanase	Hpse	Rattus norvegicus (Norway rat)
64544	beta-1,3-glucuronyltransferase 2	B3gat2	Rattus norvegicus (Norway rat)	Barrett's esophagus schizophrenia
64711	heparan sulfate-glucosamine 3-sulfotransferase 6	HS3ST6	Homo sapiens (human)	anthracosilicosis asbestosis bagassosis hereditary angioedema herpes simplex pneumoconiosis siderosis
64772	endo-beta-N-acetylglucosaminidase	ENGASE Aliases: Di-N-acetylchitobiosyl beta-N-acetylglucosaminidase FLJ21865 Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase	Homo sapiens (human)	NGLY1-deficiency breast cancer breast carcinoma rheumatoid arthritis
66967	ER degradation enhancer, mannosidase alpha-like 3	Edem3	Mus musculus (house mouse)	congenital disorder of glycosylation type II
68292	STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae)	Stt3b	Mus musculus (house mouse)	congenital disorder of glycosylation Iw congenital disorder of glycosylation Ix
68947	carbohydrate sulfotransferase 8	Chst8	Mus musculus (house mouse)
71367	carbohydrate sulfotransferase 9	Chst9	Mus musculus (house mouse)
71797	carbohydrate sulfotransferase 13	Chst13	Mus musculus (house mouse)
72136	carbohydrate sulfotransferase 14	Chst14	Mus musculus (house mouse)	Ehlers-Danlos syndrome musculocontractural type 1
72727	beta-1,3-glucuronyltransferase 3	B3gat3	Mus musculus (house mouse)	Larsen-like syndrome B3GAT3 type
76051	glucosidase, alpha; neutral C	Ganc	Mus musculus (house mouse)
76055	O-GlcNAcase	Oga	Mus musculus (house mouse)	type 2 diabetes mellitus
76898	beta-1,3-glucuronyltransferase 1	B3gat1	Mus musculus (house mouse)	pulmonary fibrosis
78752	chondroitin sulfate N-acetylgalactosaminyltransferase 2	Csgalnact2	Mus musculus (house mouse)
79158	N-acetylglucosamine-1-phosphate transferase subunits alpha and beta	GNPTAB Aliases: KIAA1208 MGC4170	Homo sapiens (human)	Ebola hemorrhagic fever Fabry disease Laron syndrome Legg-Calve-Perthes disease Scheuermann's disease achondroplasia alexia anemia aortic valve insufficiency arrhythmogenic right ventricular cardiomyopathy autistic disorder cancer capillary hemangioma cardiomyopathy cavernous hemangioma chromophobe renal cell carcinoma chylomicron retention disease clear cell renal cell carcinoma clubfoot collecting duct carcinoma congenital central hypoventilation syndrome congestive heart failure corneal dystrophy craniosynostosis disease of metabolism dyslexia embryoma endomyocardial fibrosis enterocele familial hypertrophic cardiomyopathy glycoproteinosis hemangioma hypertrophic cardiomyopathy inguinal hernia intellectual disability keratosis follicularis learning disability lipid storage disease lysosomal storage disease macrocytic anemia megalocornea mixed sleep apnea mongolian spot mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucolipidosis mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis multiple epiphyseal dysplasia nonpapillary renal cell carcinoma obstructive sleep apnea omphalocele osteochondrodysplasia papillary renal cell carcinoma pseudoxanthoma elasticum renal carcinoma renal cell carcinoma retinal degeneration retinal disease retinitis sarcomatoid renal cell carcinoma scoliosis sleep apnea spinal cord disease stuttering syringomyelia umbilical hernia
79690	galactose-3-O-sulfotransferase 4	GAL3ST4 Aliases: FLJ12116	Homo sapiens (human)	leprosy
80267	ER degradation enhancing alpha-mannosidase like protein 3	EDEM3	Homo sapiens (human)	congenital disorder of glycosylation type II hepatitis C prostate cancer prostate carcinoma
83398	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	Ndst3	Mus musculus (house mouse)	autism spectrum disorder azoospermia intellectual disability
83539	carbohydrate sulfotransferase 9	CHST9 Aliases: GALNAC-4-ST2 GALNAC4ST-2	Homo sapiens (human)	acute lymphoblastic leukemia acute myeloid leukemia breast cancer breast carcinoma cancer coronary artery disease depressive disorder essential thrombocythemia hematologic cancer idiopathic scoliosis lymphoblastic lymphoma major depressive disorder melancholic depression myelodysplastic syndrome obsolete melancholia schizophrenia
84406	heparan sulfate-glucosamine 3-sulfotransferase 1	Hs3st1	Rattus norvegicus (Norway rat)
84572	N-acetylglucosamine-1-phosphate transferase subunit gamma	GNPTG Aliases: CAB56184 GlcNAc-phosphotransferase gamma-subunit c316G12.3	Homo sapiens (human)	Fabry disease Laron syndrome achondroplasia alexia aortic valve disease 2 aortic valve insufficiency aortic valve stenosis chylomicron retention disease cone-rod dystrophy dyslexia fundus albipunctatus glycoproteinosis lipid storage disease lysosomal storage disease mucolipidosis II alpha/beta mucolipidosis III alpha/beta mucolipidosis III gamma mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis myopia osteochondrodysplasia retinitis pigmentosa scoliosis stuttering

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