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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	October 29, 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 **1 - 25** of **17989** in total

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Gene ID	Gene Name	Gene Symbol	Organism	Disease Ontology ▲
25608	leptin	Lep	Rattus norvegicus (Norway rat)	Alzheimer's disease Parkinson's disease alcohol dependence alcoholic liver cirrhosis glucose intolerance hepatocellular carcinoma hyperinsulinism hypertension hypogonadism obesity osteoporosis short bowel syndrome type 2 diabetes mellitus
695	Bruton tyrosine kinase	BTK	Homo sapiens (human)	B-cell lymphoma Burkitt lymphoma X-linked agammaglobulinemia agammaglobulinemia central nervous system lymphoma isolated growth hormone deficiency type III mantle cell lymphoma
4321	matrix metallopeptidase 12	MMP12	Homo sapiens (human)	Barrett's esophagus abdominal aortic aneurysm arteriosclerosis coronary aneurysm coronary artery disease esophagus adenocarcinoma multiple sclerosis
135152	beta-1,3-glucuronyltransferase 2	B3GAT2 Aliases: GlcAT-S galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 2 glucuronosyltransferase S	Homo sapiens (human)	Barrett's esophagus schizophrenia
4669	N-acetyl-alpha-glucosaminidase	NAGLU Aliases: NAG Sanfilippo disease IIIB	Homo sapiens (human)	Charcot-Marie-Tooth disease axonal type 2V mucopolysaccharidosis III mucopolysaccharidosis type IIIB
124583	calcium activated nucleotidase 1	CANT1 Aliases: SCAN-1 SHAPY Soluble Ca-Activated Nucleotidase, isozyme 1 apyrase 1 homolog (C. lectularius)	Homo sapiens (human)	Desbuquois dysplasia multiple epiphyseal dysplasia 7
64131	xylosyltransferase 1	XYLT1 Aliases: PXYLT1 XT-I protein xylosyltransferase 1	Homo sapiens (human)	Desbuquois dysplasia pseudoxanthoma elasticum type 1 diabetes mellitus
76025	calcium activated nucleotidase 1	Cant1	Mus musculus (house mouse)	Desbuquois dysplasia
15531	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1	Ndst1	Mus musculus (house mouse)	DiGeorge syndrome congenital diaphragmatic hernia newborn respiratory distress syndrome
113189	carbohydrate sulfotransferase 14	CHST14 Aliases: D4ST-1 HD4ST	Homo sapiens (human)	Ehlers-Danlos syndrome musculocontractural type 1
29940	dermatan sulfate epimerase	DSE Aliases: DS-Epi1 DSEPI	Homo sapiens (human)	Ehlers-Danlos syndrome musculocontractural type 2
11285	beta-1,4-galactosyltransferase 7	B4GALT7 Aliases: XGALT-1 beta4Gal-T7 galactosyltransferase I	Homo sapiens (human)	Ehlers-Danlos syndrome spondylodysplastic type 1 Ehlers-Danlos syndrome
126792	beta-1,3-galactosyltransferase 6	B3GALT6 Aliases: beta-1,3-galactosyltransferase-6 beta3GalT6	Homo sapiens (human)	Ehlers-Danlos syndrome spondylodysplastic type 2 spondyloepimetaphyseal dysplasia with joint laxity type 1
445022	xylosylprotein beta 1,4-galactosyltransferase, polypeptide 7 (galactosyltransferase I)	b4galt7	Danio rerio (zebrafish)	Ehlers-Danlos syndrome
176382	Xylosylprotein 4-beta-galactosyltransferase	sqv-3	Caenorhabditis elegans	Ehlers-Danlos syndrome
6569	solute carrier family 34 member 1	SLC34A1	Homo sapiens (human)	Fanconi renotubular syndrome 2 Fanconi syndrome chronic kidney disease hereditary hypophosphatemic rickets with hypercalciuria hypercalcemia hypophosphatemic nephrolithiasis/osteoporosis 1 nephrolithiasis
246179	fukutin	Fktn	Mus musculus (house mouse)	Fukuyama congenital muscular dystrophy muscular dystrophy-dystroglycanopathy type B1
2720	galactosidase beta 1	GLB1 Aliases: EBP elastin binding protein	Homo sapiens (human)	GM1 gangliosidosis type 1 GM1 gangliosidosis type 2 GM1 gangliosidosis type 3 GM1 gangliosidosis mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis type IVB
12091	galactosidase, beta 1	Glb1	Mus musculus (house mouse)	GM1 gangliosidosis
16147	Indian hedgehog	Ihh	Mus musculus (house mouse)	Hirschsprung's disease annular pancreas brachydactyly type A1
14595	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	B4galt1	Mus musculus (house mouse)	IgA glomerulonephritis endocrine system disease
1280	collagen type II alpha 1 chain	COL2A1	Homo sapiens (human)	Kniest dysplasia Legg-Calve-Perthes disease Stickler syndrome 1 Stickler syndrome Torrance type platyspondylic dysplasia achondrogenesis type II chondrosarcoma chorioretinitis cleft palate eye disease multiple epiphyseal dysplasia with myopia and deafness myopia osteoarthritis osteochondrodysplasia osteonecrosis retinal detachment spondyloarthropathy spondyloepimetaphyseal dysplasia, Strudwick type spondyloepiphyseal dysplasia Stanescu type spondyloepiphyseal dysplasia congenita spondyloperipheral dysplasia
26229	beta-1,3-glucuronyltransferase 3	B3GAT3 Aliases: GlcAT-I galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 3 glucuronosyltransferase I	Homo sapiens (human)	Larsen-like syndrome B3GAT3 type
1301	collagen type XI alpha 1 chain	COL11A1	Homo sapiens (human)	Marshall syndrome Stickler syndrome 2 autosomal dominant nonsyndromic deafness 37 fibrochondrogenesis 1
11977	ATPase, copper transporting, alpha polypeptide	Atp7a	Mus musculus (house mouse)	Menkes disease X-linked distal spinal muscular atrophy 3 aortic aneurysm osteoarthritis

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