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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 **176 - 200** of **17827** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
89792	galactose-3-O-sulfotransferase 3	GAL3ST3 Aliases: GAL3ST2	Homo sapiens (human)
90161	heparan sulfate 6-O-sulfotransferase 2	HS6ST2 Aliases: HS6ST-2	Homo sapiens (human)	Paganini-Miozzo syndrome arthritis arthropathy idiopathic interstitial pneumonia idiopathic pulmonary fibrosis intellectual disability learning disability lung adenocarcinoma lung cancer myopia osteoarthritis stomach cancer stomach carcinoma
92370	2-phosphoxylose phosphatase 1	PXYLP1 Aliases: FLJ23751	Homo sapiens (human)	myopia
93611	F-box protein 44	FBXO44 Aliases: FBG3 FBX30 Fbx44 Fbxo6a MGC14140	Homo sapiens (human)	polycystic ovary syndrome prostate cancer prostate carcinoma
98388	carbohydrate sulfotransferase 10	Chst10	Mus musculus (house mouse)
108687	ER degradation enhancer, mannosidase alpha-like 2	Edem2	Mus musculus (house mouse)
110006	glucuronidase, beta	Gusb	Mus musculus (house mouse)	Sly syndrome mucopolysaccharidosis peritonitis
110173	mannosidase, beta A, lysosomal	Manba	Mus musculus (house mouse)	beta-mannosidosis
113189	carbohydrate sulfotransferase 14	CHST14 Aliases: D4ST-1 HD4ST	Homo sapiens (human)	Ehlers-Danlos syndrome musculocontractural type 1 Ehlers-Danlos syndrome Marfan syndrome Peters anomaly agnosia arthropathy atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect brittle cornea syndrome 1 cleft palate clubfoot congenital diaphragmatic hernia cornea plana craniosynostosis cryptorchidism developmental coordination disorder distal arthrogryposis familial nephrotic syndrome familial periodic paralysis glaucoma hiatus hernia hydrocephalus hydronephrosis hypertropia isolated cleft palate lipoid nephrosis mechanical strabismus myopathy myopia nephrotic syndrome obsolete constipation omphalocele ophthalmoplegia osteogenesis imperfecta patent foramen ovale pneumothorax prostate cancer prostate carcinoma retinal detachment scoliosis sensorineural hearing loss situs inversus strabismus tuberous sclerosis umbilical hernia
114002	N-deacetylase and N-sulfotransferase 2	Ndst2	Rattus norvegicus (Norway rat)	autism spectrum disorder azoospermia intellectual disability
115290	F-box protein 17	FBXO17 Aliases: F-box only protein 26 FBG4 FLJ11798 FLJ25205 Fbx17 MGC9379	Homo sapiens (human)	cancer embryoma gliosarcoma hepatocellular carcinoma high grade glioma liver cancer lung cancer lung non-small cell carcinoma mixed glioma
116696	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 4	St8sia4	Rattus norvegicus (Norway rat)
117108	beta-1,3-glucuronyltransferase 1	B3gat1	Rattus norvegicus (Norway rat)	pulmonary fibrosis
117523	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	St8sia2	Rattus norvegicus (Norway rat)
117592	UDP-Gal:betaGal beta 1,3-galactosyltransferase, polypeptide 6	B3galt6	Mus musculus (house mouse)	Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome spondyloepimetaphyseal dysplasia with joint laxity type 1
126792	beta-1,3-galactosyltransferase 6	B3GALT6 Aliases: beta-1,3-galactosyltransferase-6 beta3GalT6	Homo sapiens (human)	Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome Hailey-Hailey disease Hirschsprung's disease Laron syndrome Rothmund-Thomson syndrome achondroplasia aortic valve disease 1 aortic valve disease 2 aortic valve stenosis atrial heart septal defect 1 atrial heart septal defect 2 atrial heart septal defect 3 atrial heart septal defect 4 atrial heart septal defect 5 atrial heart septal defect 6 atrial heart septal defect 7 atrial heart septal defect 8 atrial heart septal defect 9 atrial heart septal defect autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive cutis laxa type IA autosomal recessive cutis laxa type IB autosomal recessive cutis laxa type II classic type autosomal recessive cutis laxa type IIA autosomal recessive cutis laxa type IIB autosomal recessive cutis laxa type IIC autosomal recessive cutis laxa type IID autosomal recessive cutis laxa type IIIA autosomal recessive cutis laxa type IIIB bicuspid aortic valve disease bone disease cartilage disease cherubism chondrodysplasia punctata chromophobe renal cell carcinoma clear cell renal cell carcinoma cleft palate clubfoot collagen disease collecting duct carcinoma connective tissue disease cutis laxa enophthalmos exostosis heart septal defect hepatocellular carcinoma intellectual disability isolated cleft palate isolated ectopia lentis learning disability liver cancer mal de Meleda mitral valve insufficiency mitral valve prolapse myopia nonpapillary renal cell carcinoma obsolete exophthalmos orbital disease osteogenesis imperfecta osteoporosis papillary renal cell carcinoma paraplegia patent foramen ovale periarthritis renal carcinoma renal cell carcinoma restrictive dermopathy sarcomatoid renal cell carcinoma scoliosis spinal cord disease spondyloepimetaphyseal dysplasia with joint laxity type 1 tendinitis ventricular septal defect
129807	neuraminidase 4	NEU4	Homo sapiens (human)	cancer embryoma giant cell glioblastoma glioblastoma high grade glioma neuroblastoma
135152	beta-1,3-glucuronyltransferase 2	B3GAT2 Aliases: GlcAT-S galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 2 glucuronosyltransferase S	Homo sapiens (human)	Barrett's esophagus schizophrenia thrombophilia
138050	heparan-alpha-glucosaminide N-acetyltransferase	HGSNAT Aliases: FLJ32731 HGNAT	Homo sapiens (human)	Zollinger-Ellison syndrome agnosia amnestic disorder blindness bulimia nervosa cataract cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness corneal disease developmental coordination disorder diabetes mellitus diarrhea dissociated nystagmus echolalia enterocele epilepsy fundus albipunctatus fundus dystrophy glaucoma hyperinsulinism hypertrichosis hypertrophic cardiomyopathy 1 hypogonadism intellectual disability keratoconus learning disability mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis type IIIB mucopolysaccharidosis type IIIC mucopolysaccharidosis type IIID mucopolysaccharidosis night blindness obesity obsolete asthenopia ophthalmoplegia optic atrophy pathologic nystagmus peripheral retinal degeneration retinitis pigmentosa 73 retinitis pigmentosa retrograde amnesia scoliosis sensorineural hearing loss spontaneous ocular nystagmus stereotypic movement disorder type 2 diabetes mellitus visual epilepsy
140481	mannosidase 2, alpha 2	Man2a2	Mus musculus (house mouse)	schizophrenia
140568	carbohydrate sulfotransferase 10	Chst10	Rattus norvegicus (Norway rat)
154968	O-GlcNAcase	Oga	Rattus norvegicus (Norway rat)	type 2 diabetes mellitus
166012	carbohydrate sulfotransferase 13	CHST13 Aliases: C4ST3 chondroitin 4-sulfotransferase 3	Homo sapiens (human)	arthritis arthropathy osteoarthritis primary pulmonary hypertension
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
174517	Galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase sqv-8	sqv-8	Caenorhabditis elegans	Barrett's esophagus Larsen-like syndrome B3GAT3 type pulmonary fibrosis schizophrenia

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