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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 **51 - 75** of **17827** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
11282	alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B	MGAT4B Aliases: GnT-Ivb	Homo sapiens (human)	cancer depressive disorder embryoma major depressive disorder melancholic depression obsolete melancholia
11285	beta-1,4-galactosyltransferase 7	B4GALT7 Aliases: XGALT-1 beta4Gal-T7 galactosyltransferase I	Homo sapiens (human)	Cockayne syndrome Cornelia de Lange syndrome Dubowitz syndrome Ehlers-Danlos syndrome spondylodysplastic type 1 Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome Hailey-Hailey disease IgA glomerulonephritis Laron syndrome Larsen-like syndrome B3GAT3 type Noonan syndrome 10 Noonan syndrome 1 Noonan syndrome 2 Noonan syndrome 3 Noonan syndrome 4 Noonan syndrome 5 Noonan syndrome 6 Noonan syndrome 7 Noonan syndrome 8 Noonan syndrome 9 Noonan syndrome Prader-Willi syndrome Robinow syndrome Rothmund-Thomson syndrome Seckel syndrome Silver-Russell syndrome X-linked Aarskog syndrome achondroplasia aortic valve disease 2 aortic valve stenosis arthritis arthropathy autosomal dominant Robinow syndrome 1 autosomal dominant Robinow syndrome 2 autosomal dominant Robinow syndrome 3 autosomal dominant cutis laxa 1 autosomal dominant cutis laxa 2 autosomal dominant cutis laxa 3 autosomal dominant cutis laxa autosomal recessive Robinow syndrome 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 bone disease cartilage disease chondrodysplasia-pseudohermaphroditism syndrome cleidocranial dysplasia clubfoot colitis collagen disease coloboma congenital disorder of glycosylation type IId congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 connective tissue disease cryptorchidism cutis laxa enophthalmos gastroenteritis gingivitis hepatocellular carcinoma humeroradial synostosis ileitis ileocolitis lipoatrophic diabetes mellitus lipodystrophy liver cancer mal de Meleda microcephalic osteodysplastic primordial dwarfism type I microcephalic osteodysplastic primordial dwarfism type II mucopolysaccharidosis IV multiple epiphyseal dysplasia obsolete exophthalmos orbital disease osteoarthritis osteochondrodysplasia osteogenesis imperfecta pulmonary valve stenosis radioulnar synostosis restrictive dermopathy rheumatoid arthritis scoliosis skin disease spermatic cord torsion trichohepatoenteric syndrome 1 trichohepatoenteric syndrome
11320	alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase A	MGAT4A Aliases: GnT-4a GnT-Iva	Homo sapiens (human)	bipolar disorder cancer colorectal cancer diabetes mellitus disease of metabolism embryoma gestational trophoblastic neoplasm hypoplastic left heart syndrome large intestine cancer pancreatic cancer type 2 diabetes mellitus
14042	exostosin glycosyltransferase 1	Ext1	Mus musculus (house mouse)	autism spectrum disorder chondrosarcoma hereditary multiple exostoses
14043	exostosin glycosyltransferase 2	Ext2	Mus musculus (house mouse)	hereditary multiple exostoses
14376	alpha glucosidase 2 alpha neutral subunit	Ganab	Mus musculus (house mouse)	polycystic kidney disease 3 polycystic kidney disease polycystic liver disease
14537	glucosaminyl (N-acetyl) transferase 1, core 2	Gcnt1	Mus musculus (house mouse)
14595	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	B4galt1	Mus musculus (house mouse)	IgA glomerulonephritis congenital disorder of glycosylation type IId congenital disorder of glycosylation endocrine system disease
15442	heparanase	Hpse	Mus musculus (house mouse)
15476	heparan sulfate (glucosamine) 3-O-sulfotransferase 1	Hs3st1	Mus musculus (house mouse)
15478	heparan sulfate (glucosamine) 3-O-sulfotransferase 3A1	Hs3st3a1	Mus musculus (house mouse)
15531	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1	Ndst1	Mus musculus (house mouse)	DiGeorge syndrome autism spectrum disorder autosomal recessive intellectual developmental disorder 46 azoospermia congenital diaphragmatic hernia intellectual disability newborn respiratory distress syndrome
16795	LARGE xylosyl- and glucuronyltransferase 1	Large1	Mus musculus (house mouse)	congenital muscular dystrophy-dystroglycanopathy type A6 facioscapulohumeral muscular dystrophy muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B6
16846	leptin	Lep	Mus musculus (house mouse)	Alzheimer's disease Huntington's disease Parkinson's disease abdominal obesity-metabolic syndrome 1 abdominal obesity-metabolic syndrome acute pancreatitis adult respiratory distress syndrome alcohol dependence alcoholic liver cirrhosis asthma breast cancer chronic obstructive pulmonary disease congenital leptin deficiency cystic fibrosis end stage renal disease familial hyperlipidemia gestational diabetes glucose intolerance hepatocellular carcinoma hepatocellular clear cell carcinoma hyperinsulinism hypertension hypogonadism lipid metabolism disorder lung non-small cell carcinoma metabolic dysfunction-associated steatotic liver disease obesity obstructive sleep apnea osteoarthritis osteoporosis pre-eclampsia primary biliary cholangitis renal cell carcinoma rhinitis short bowel syndrome steatotic liver disease type 2 diabetes mellitus
17155	mannosidase 1, alpha	Man1a	Mus musculus (house mouse)
17156	mannosidase, alpha, class 1A, member 2	Man1a2	Mus musculus (house mouse)
17158	mannosidase 2, alpha 1	Man2a1	Mus musculus (house mouse)	congenital dyserythropoietic anemia systemic lupus erythematosus
17159	mannosidase 2, alpha B1	Man2b1	Mus musculus (house mouse)	alpha-mannosidosis
17423	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2	Ndst2	Mus musculus (house mouse)	autism spectrum disorder azoospermia intellectual disability
20443	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	St3gal4	Mus musculus (house mouse)
20444	ST3 beta-galactoside alpha-2,3-sialyltransferase 2	St3gal2	Mus musculus (house mouse)
20447	ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase 3	St6galnac3	Mus musculus (house mouse)
20449	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1	St8sia1	Mus musculus (house mouse)
20450	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 2	St8sia2	Mus musculus (house mouse)
20451	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3	St8sia3	Mus musculus (house mouse)

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