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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

Displaying entries **9576 - 9600** of **9988** in total

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Gene ID	Gene Name	Gene Symbol	Organism ▲	Disease Ontology
408	arrestin beta 1	ARRB1	Homo sapiens (human)
94120	synaptotagmin like 3	SYTL3	Homo sapiens (human)
79778	MICAL like 2	MICALL2	Homo sapiens (human)
9966	TNF superfamily member 15	TNFSF15	Homo sapiens (human)
11152	WD repeat domain 45	WDR45	Homo sapiens (human)
11112	3-hydroxyisobutyrate dehydrogenase	HIBADH	Homo sapiens (human)
2288	FKBP prolyl isomerase 4	FKBP4	Homo sapiens (human)
10488	cAMP responsive element binding protein 3	CREB3	Homo sapiens (human)
57181	solute carrier family 39 member 10	SLC39A10	Homo sapiens (human)
65989	delta like non-canonical Notch ligand 2	DLK2	Homo sapiens (human)
775	calcium voltage-gated channel subunit alpha1 C	CACNA1C	Homo sapiens (human)
1440	colony stimulating factor 3	CSF3	Homo sapiens (human)
29909	G protein-coupled receptor 171	GPR171	Homo sapiens (human)
114771	peptidoglycan recognition protein 3	PGLYRP3	Homo sapiens (human)
1397	cysteine rich protein 2	CRIP2	Homo sapiens (human)
127059	olfactory receptor family 2 subfamily M member 5	OR2M5	Homo sapiens (human)
26659	olfactory receptor family 7 subfamily A member 5	OR7A5	Homo sapiens (human)
9340	glucagon like peptide 2 receptor	GLP2R	Homo sapiens (human)
844	calsequestrin 1	CASQ1	Homo sapiens (human)
55150	chromosome 19 open reading frame 73	C19orf73	Homo sapiens (human)
56242	zinc finger protein 253	ZNF253	Homo sapiens (human)
54823	SWT1 RNA endoribonuclease homolog	SWT1	Homo sapiens (human)
80301	pleckstrin homology domain containing O2	PLEKHO2	Homo sapiens (human)
26229	beta-1,3-glucuronyltransferase 3	B3GAT3 Aliases: GlcAT-I galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 3 glucuronosyltransferase I	Homo sapiens (human)	Hailey-Hailey disease Laron syndrome Larsen-like syndrome B3GAT3 type Marfan syndrome Rothmund-Thomson syndrome achondroplasia amblyopia 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 buphthalmos cancer cleft palate cleidocranial dysplasia clubfoot communicating hydrocephalus congenital heart disease craniosynostosis cutis laxa esotropia geroderma osteodysplasticum glaucoma hepatocellular carcinoma humeroradial synostosis hydrocephalus hydrophthalmos hyperopia idiopathic interstitial pneumonia idiopathic pulmonary fibrosis isolated cleft palate juvenile glaucoma liver cancer liver carcinoma mal de Meleda mitral valve insufficiency mitral valve prolapse monocular esotropia mucopolysaccharidosis IV multiple epiphyseal dysplasia obstructive hydrocephalus osteochondrodysplasia osteoporosis patent foramen ovale postinflammatory pulmonary fibrosis postural orthostatic tachycardia syndrome pulmonary fibrosis radioulnar synostosis refractive error restrictive dermopathy scoliosis senile degeneration of brain situs inversus strabismic amblyopia thoracic aortic aneurysm tuberous sclerosis
6853	synapsin I	SYN1	Homo sapiens (human)

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