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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 **414201 - 414225** of **422592** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
26279	phospholipase A2 group IID	PLA2G2D Aliases: sPLA2S	Homo sapiens (human)	Down syndrome arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease ascending cholangitis atherosclerosis breast cancer cancer cholangitis chronic obstructive pulmonary disease colon cancer colon carcinoma colonic benign neoplasm colorectal cancer coronary artery disease embryoma large intestine cancer primary sclerosing cholangitis sclerosing cholangitis suppurative cholangitis
26278	sacsin molecular chaperone	SACS	Homo sapiens (human)
26276	VPS33B late endosome and lysosome associated	VPS33B	Homo sapiens (human)
26275	3-hydroxyisobutyryl-CoA hydrolase	HIBCH	Homo sapiens (human)	Leigh disease Unverricht-Lundborg syndrome West syndrome agnosia arthritis arthropathy blepharospasm brain disease cancer colorectal cancer colorectal carcinoma congenital nystagmus cryptorchidism developmental coordination disorder dissociated nystagmus dystonia early myoclonic encephalopathy epilepsy focal hand dystonia generalized dystonia hydrocephalus hypertropia inherited metabolic disorder lactic acidosis large intestine cancer mechanical strabismus neurodegenerative disease obsolete infantile epileptic encephalopathy ophthalmoplegia osteoarthritis pathologic nystagmus spontaneous ocular nystagmus strabismus tetralogy of Fallot visual epilepsy
26271	F-box protein 5	FBXO5	Homo sapiens (human)
26262	tetraspanin 17	TSPAN17	Homo sapiens (human)
26256	calcium binding tyrosine phosphorylation regulated	CABYR	Homo sapiens (human)
26254	opticin	OPTC	Homo sapiens (human)
26253	C-type lectin domain family 4 member E	CLEC4E Aliases: MINCLE Macrophage-inducible C-type lectin	Homo sapiens (human)	acute myocardial infarction allergic asthma arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease arthritis arthropathy asthma atherosclerosis coronary thrombosis depressive disorder dysthymic disorder intrinsic asthma keratitis keratoconjunctivitis major depressive disorder melancholic depression multiple sclerosis mycotic corneal ulcer myocardial infarction neurotic disorder obsolete melancholia pulmonary tuberculosis rheumatoid arthritis silent myocardial infarction tuberculosis tuberculous pneumothorax
26248	olfactory receptor family 2 subfamily K member 2	OR2K2	Homo sapiens (human)
26246	olfactory receptor family 2 subfamily L member 2	OR2L2	Homo sapiens (human)
26245	olfactory receptor family 2 subfamily M member 4	OR2M4	Homo sapiens (human)
26235	F-box and leucine rich repeat protein 4	FBXL4	Homo sapiens (human)
26233	F-box and leucine rich repeat protein 6	FBXL6	Homo sapiens (human)
26232	F-box protein 2	FBXO2 Aliases: FBX2 Fbg1 Fbs1 Nfb42	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease Pick's disease Reye syndrome cerebral degeneration hyperglycemia rheumatoid arthritis stomach cancer stomach carcinoma
26230	TIAM Rac1 associated GEF 2	TIAM2	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
26227	phosphoglycerate dehydrogenase	PHGDH	Homo sapiens (human)
26219	olfactory receptor family 1 subfamily J member 4	OR1J4	Homo sapiens (human)
26212	olfactory receptor family 2 subfamily B member 6	OR2B6	Homo sapiens (human)
26211	olfactory receptor family 2 subfamily F member 1	OR2F1	Homo sapiens (human)
26205	glucocorticoid modulatory element binding protein 2	GMEB2	Homo sapiens (human)
26201	NADH dehydrogenase subunit 4	ND4	Rattus norvegicus (Norway rat)
26195	cytochrome c oxidase subunit I	COX1	Rattus norvegicus (Norway rat)
26189	olfactory receptor family 1 subfamily A member 2	OR1A2	Homo sapiens (human)

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