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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

Displaying entries **2251 - 2275** of **393515** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
108150	polypeptide N-acetylgalactosaminyltransferase 7	Galnt7	Mus musculus (house mouse)
108155	O-linked N-acetylglucosamine (GlcNAc) transferase (UDP-N-acetylglucosamine:polypeptide-N-acetylglucosaminyl transferase)	Ogt	Mus musculus (house mouse)	aortic valve stenosis congestive heart failure diabetes mellitus non-syndromic X-linked intellectual disability 106 type 2 diabetes mellitus
108645	methionine adenosyltransferase 2 non-catalytic beta subunit methionine	Mat2b	Mus musculus (house mouse)
108687	ER degradation enhancer, mannosidase alpha-like 2	Edem2	Mus musculus (house mouse)
108760	polypeptide N-acetylgalactosaminyltransferase 16	Galnt16	Mus musculus (house mouse)
108902	beta-1,4-glucuronyltransferase 1	B4gat1	Mus musculus (house mouse)	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A13 muscular dystrophy-dystroglycanopathy type B1
109685	hyaluronoglucosaminidase 3	Hyal3	Mus musculus (house mouse)
109785	phosphoglucomutase 3	Pgm3	Mus musculus (house mouse)	cancer cervical cancer immunodeficiency 23 teratoma
109880	Braf transforming gene	Braf	Mus musculus (house mouse)	Langerhans-cell histiocytosis Noonan syndrome 7 Noonan syndrome with multiple lentigines 3 bile duct adenoma cancer cardiofaciocutaneous syndrome 1 cardiofaciocutaneous syndrome cardiomyopathy cholangiocarcinoma colon carcinoma colorectal adenocarcinoma colorectal cancer dysembryoplastic neuroepithelial tumor endometrial carcinoma familial melanoma germinoma high grade glioma intrahepatic cholangiocarcinoma lung cancer malignant astrocytoma melanoma pancreatic acinar cell adenocarcinoma pancreatic cancer pleomorphic xanthoastrocytoma prostate adenocarcinoma thyroid gland papillary carcinoma
109959	amylase 2a5	Amy2a5	Mus musculus (house mouse)
109978	ADP-ribosyltransferase 4	Art4	Mus musculus (house mouse)
109979	ADP-ribosyltransferase 3	Art3	Mus musculus (house mouse)
110006	glucuronidase, beta	Gusb	Mus musculus (house mouse)	Sly syndrome mucopolysaccharidosis peritonitis
110078	brain glycogen phosphorylase	Pygb	Mus musculus (house mouse)
110094	phosphorylase kinase alpha 2	Phka2	Mus musculus (house mouse)	glycogen storage disease IXa glycogen storage disease visceral heterotaxy
110095	liver glycogen phosphorylase	Pygl	Mus musculus (house mouse)	glycogen storage disease VI glycogen storage disease lactic acidosis
110119	mannose phosphate isomerase	Mpi	Mus musculus (house mouse)	carbohydrate metabolic disorder congenital disorder of glycosylation Ib congenital disorder of glycosylation type I
110173	mannosidase, beta A, lysosomal	Manba	Mus musculus (house mouse)	beta-mannosidosis
110208	phosphogluconate dehydrogenase	Pgd	Mus musculus (house mouse)
112417	UDP glucuronosyltransferase 2 family, polypeptide B37	Ugt2b37	Mus musculus (house mouse)
112817	4-hydroxy-2-oxoglutarate aldolase 1	HOGA1 Aliases: DHDPS2 FLJ37472 N-acetylneuraminate pyruvate lyase 2 (putative) NPL2 dihydrodipicolinate synthetase homolog 2 (E. coli)	Homo sapiens (human)	calcinosis calcium metabolism disease cholestasis chronic kidney disease hypercalcemia nephrocalcinosis nephrolithiasis phosphorus metabolism disease primary hyperoxaluria type 3 primary hyperoxaluria
112937	galactosidase beta 1 like 3	GLB1L3 Aliases: FLJ90231	Homo sapiens (human)
113026	phospholipase C delta 3	PLCD3	Homo sapiens (human)	Goldenhar syndrome acquired immunodeficiency syndrome alcohol dependence alcohol use disorder arteriosclerotic cardiovascular disease atherosclerosis coronary artery disease human immunodeficiency virus infectious disease microphthalmia nasopharynx carcinoma obsolete Matthew-Wood syndrome senile cataract
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
113612	cytochrome P450 family 2 subfamily U member 1	CYP2U1 Aliases: SPG49 spastic paraplegia 49	Homo sapiens (human)	Charcot-Marie-Tooth disease type 5 GM1 gangliosidosis type 1 GM1 gangliosidosis Henoch-Schoenlein purpura MASA syndrome Mast syndrome SPOAN syndrome Troyer syndrome agnosia blindness breast cancer breast carcinoma cancer developmental coordination disorder dystonia embryoma focal hand dystonia generalized dystonia hereditary spastic paraplegia 10 hereditary spastic paraplegia 11 hereditary spastic paraplegia 12 hereditary spastic paraplegia 13 hereditary spastic paraplegia 14 hereditary spastic paraplegia 15 hereditary spastic paraplegia 16 hereditary spastic paraplegia 17 hereditary spastic paraplegia 18 hereditary spastic paraplegia 19 hereditary spastic paraplegia 23 hereditary spastic paraplegia 24 hereditary spastic paraplegia 25 hereditary spastic paraplegia 26 hereditary spastic paraplegia 27 hereditary spastic paraplegia 28 hereditary spastic paraplegia 29 hereditary spastic paraplegia 2 hereditary spastic paraplegia 30 hereditary spastic paraplegia 31 hereditary spastic paraplegia 32 hereditary spastic paraplegia 34 hereditary spastic paraplegia 35 hereditary spastic paraplegia 36 hereditary spastic paraplegia 37 hereditary spastic paraplegia 38 hereditary spastic paraplegia 39 hereditary spastic paraplegia 3A hereditary spastic paraplegia 41 hereditary spastic paraplegia 42 hereditary spastic paraplegia 43 hereditary spastic paraplegia 44 hereditary spastic paraplegia 45 hereditary spastic paraplegia 46 hereditary spastic paraplegia 48 hereditary spastic paraplegia 49 hereditary spastic paraplegia 4 hereditary spastic paraplegia 53 hereditary spastic paraplegia 54 hereditary spastic paraplegia 55 hereditary spastic paraplegia 56 hereditary spastic paraplegia 57 hereditary spastic paraplegia 5A hereditary spastic paraplegia 61 hereditary spastic paraplegia 62 hereditary spastic paraplegia 63 hereditary spastic paraplegia 64 hereditary spastic paraplegia 6 hereditary spastic paraplegia 72A hereditary spastic paraplegia 73 hereditary spastic paraplegia 75 hereditary spastic paraplegia 77 hereditary spastic paraplegia 7 hereditary spastic paraplegia 8 hereditary spastic paraplegia 9A hereditary spastic paraplegia 9B hereditary spastic paraplegia hypersensitivity vasculitis intellectual disability learning disability neurodegenerative disease neuropathy paraplegia peripheral nervous system disease polyneuropathy syringomyelia

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