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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 "glycosyltransferase activity"

Displaying entries **601 - 625** of **140293** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
148789	beta-1,3-N-acetylgalactosaminyltransferase 2	B3GALNT2 Aliases: MGC39558	Homo sapiens (human)	Dandy-Walker syndrome Duchenne muscular dystrophy Fukuyama congenital muscular dystrophy Joubert syndrome Miller-Dieker lissencephaly syndrome Peters anomaly Walker-Warburg syndrome agnosia autosomal dominant Emery-Dreifuss muscular dystrophy 2 autosomal dominant limb-girdle muscular dystrophy type 1 autosomal dominant limb-girdle muscular dystrophy type 1H autosomal dominant limb-girdle muscular dystrophy type 2 autosomal dominant limb-girdle muscular dystrophy type 3 autosomal dominant limb-girdle muscular dystrophy autosomal recessive limb-girdle muscular dystrophy type 2A autosomal recessive limb-girdle muscular dystrophy type 2B autosomal recessive limb-girdle muscular dystrophy type 2C autosomal recessive limb-girdle muscular dystrophy type 2D autosomal recessive limb-girdle muscular dystrophy type 2E autosomal recessive limb-girdle muscular dystrophy type 2F autosomal recessive limb-girdle muscular dystrophy type 2G autosomal recessive limb-girdle muscular dystrophy type 2H autosomal recessive limb-girdle muscular dystrophy type 2I autosomal recessive limb-girdle muscular dystrophy type 2J autosomal recessive limb-girdle muscular dystrophy type 2K autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy type 2O autosomal recessive limb-girdle muscular dystrophy type 2P autosomal recessive limb-girdle muscular dystrophy type 2Q autosomal recessive limb-girdle muscular dystrophy type 2S autosomal recessive limb-girdle muscular dystrophy type 2T autosomal recessive limb-girdle muscular dystrophy type 2U autosomal recessive limb-girdle muscular dystrophy type 2Y autosomal recessive limb-girdle muscular dystrophy bilateral optic nerve hypoplasia blindness breast cancer breast carcinoma cancer cataract cerebral degeneration choreatic disease coloboma communicating hydrocephalus complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congenital muscular dystrophy-dystroglycanopathy type A11 congenital muscular dystrophy-dystroglycanopathy type A1 congenital muscular dystrophy cornea plana cortical dysplasia-focal epilepsy syndrome cryptorchidism depressive disorder developmental coordination disorder distal myopathy dysthymic disorder dystonia embryoma epilepsy facioscapulohumeral muscular dystrophy familial periodic paralysis focal epilepsy fundus dystrophy glaucoma hepatocellular carcinoma holoprosencephaly 1 holoprosencephaly hydranencephaly hydrocephalus hypertropia intellectual disability isolated elevated serum creatine phosphokinase levels learning disability limb-girdle muscular dystrophy lingual-facial-buccal dyskinesia lissencephaly liver cancer major depressive disorder mechanical strabismus melancholic depression meningocele microcephaly microphthalmia muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy myopia neurotic disorder obsolete autosomal dominant limb-girdle muscular dystrophy type 1A obsolete autosomal dominant limb-girdle muscular dystrophy type 1B obsolete autosomal dominant limb-girdle muscular dystrophy type 1C obsolete autosomal recessive limb-girdle muscular dystrophy type 2R obsolete infantile epileptic encephalopathy obsolete melancholia obstructive hydrocephalus oculopharyngeal muscular dystrophy ophthalmoplegia optic atrophy partial motor epilepsy pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 recurrent corneal erosion retinal detachment rippling muscle disease 2 senile degeneration of brain sensorineural hearing loss septooptic dysplasia short-rib thoracic dysplasia 14 with polydactyly speech disorder stereotypic movement disorder strabismus syndromic X-linked intellectual disability 94 syndromic X-linked intellectual disability Najm type syndromic X-linked intellectual disability type 10 visual epilepsy
151531	uridine phosphorylase 2	UPP2 Aliases: UDRPASE2 UP2 UPASE2	Homo sapiens (human)	autism spectrum disorder autistic disorder cancer depressive disorder diabetes mellitus major depressive disorder melancholic depression obsolete melancholia squamous cell carcinoma tarsal-carpal coalition syndrome tongue squamous cell carcinoma transitional cell carcinoma type 2 diabetes mellitus
152002	xyloside xylosyltransferase 1	XXYLT1 Aliases: FLJ35155	Homo sapiens (human)	atrial fibrillation bronchus cancer bronchus carcinoma cancer lung adenocarcinoma lung benign neoplasm lung cancer lung carcinoma lung non-small cell carcinoma nicotine dependence obesity osteoporosis
152586	MGAT4 family member D	MGAT4D Aliases: GlcNAcT-I Inhibitory Protein GnT1IP glycosyltransferase 54 domain containing 1 mannosyl (alpha-1,3-)-glycoprotein beta-1,4-N-acetylglucosaminyltransferase family, member D	Homo sapiens (human)
154516	UDP glucuronosyltransferase 1 family, polypeptide A7C	Ugt1a7c	Rattus norvegicus (Norway rat)	alcoholic pancreatitis cholangiocarcinoma pancreatic cancer type 2 diabetes mellitus
160335	transmembrane O-mannosyltransferase targeting cadherins 2	TMTC2 Aliases: DKFZp762A217	Homo sapiens (human)	allergic asthma asthma dermatitis glaucoma intrinsic asthma low tension glaucoma mutism primary open angle glaucoma sensorineural hearing loss
160418	transmembrane O-mannosyltransferase targeting cadherins 3	TMTC3 Aliases: FLJ90492 SMILE	Homo sapiens (human)	Joubert syndrome Miller-Dieker lissencephaly syndrome acute myocardial infarction adult lymphoma agranulocytosis aortic aneurysm aortic valve insufficiency blood coagulation disease breast cancer breast carcinoma cancerophobia central nervous system lymphoma childhood lymphoma complex cortical dysplasia with other brain malformations 1 complex cortical dysplasia with other brain malformations 7 congestive heart failure coronary thrombosis cortical dysplasia-focal epilepsy syndrome dental caries dentin caries dermoid cyst of ovary dermoid cyst enterocele epilepsy focal epilepsy hydranencephaly hydrocephalus intellectual disability learning disability leukopenia lissencephaly 8 lissencephaly lung cancer lung non-small cell carcinoma lymphoma myocardial infarction myopia neutropenia obsolete malignant histiocytosis obsolete ymphosarcoma optic atrophy partial motor epilepsy periventricular nodular heterotopia pontocerebellar hypoplasia type 2D pontocerebellar hypoplasia type 7 pontocerebellar hypoplasia type 8 pontocerebellar hypoplasia type 9 pyloric stenosis septooptic dysplasia severe congenital neutropenia short-rib thoracic dysplasia 14 with polydactyly silent myocardial infarction syndromic X-linked intellectual disability Najm type visual epilepsy
165631	poly(ADP-ribose) polymerase family member 15	PARP15 Aliases: ARTD7 BAL3 FLJ40597 pART7	Homo sapiens (human)	atherosclerosis cancer depressive disorder embryoma major depressive disorder melancholic depression obsolete melancholia
167127	UDP glycosyltransferase family 3 member A2	UGT3A2	Homo sapiens (human)	colorectal cancer colorectal carcinoma large intestine cancer
168391	polypeptide N-acetylgalactosaminyltransferase like 5	GALNTL5 Aliases: GalNAc-T5L polypeptide GalNAc transferase-like 5	Homo sapiens (human)	actinic keratosis gastric adenocarcinoma male infertility seborrheic keratosis skin disease
170384	fucosyltransferase 11	FUT11 Aliases: MGC33202 alpha (1,3) fucosyltransferase	Homo sapiens (human)	bronchus cancer bronchus carcinoma chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma hepatocellular carcinoma liver cancer lung benign neoplasm lung cancer lung carcinoma nonpapillary renal cell carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma schizophrenia stomach cancer
170501	polypeptide N-acetylgalactosaminyltransferase 10	Galnt10	Rattus norvegicus (Norway rat)
170905	LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	Lfng	Rattus norvegicus (Norway rat)	spondylocostal dysostosis 3
171079	Beta-1,3-galactosyltransferase 4	B3galt4	Rattus norvegicus (Norway rat)
171129	UDP-glucose glycoprotein glucosyltransferase 1	Uggt1	Rattus norvegicus (Norway rat)
171167	fucosyltransferase 10	Fut10	Mus musculus (house mouse)
171212	polypeptide N-acetylgalactosaminyltransferase 10	Galnt10	Mus musculus (house mouse)
171553	alpha 1,3-galactosyltransferase 2	A3galt2	Rattus norvegicus (Norway rat)
172008	Orotate phosphoribosyltransferase	R12E2.11	Caenorhabditis elegans	orotic aciduria purine-pyrimidine metabolic disorder
172232	Adenine phosphoribosyltransferase;adenine phosphoribosyltransferase	aprt-1	Caenorhabditis elegans	adenine phosphoribosyltransferase deficiency hepatocellular carcinoma
172305	GPI mannosyltransferase pigv-1	pigv-1	Caenorhabditis elegans	hyperphosphatasia with impaired intellectual development syndrome 1
172360	Alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase	gly-2	Caenorhabditis elegans	proteinuria
172475	Glycosyltransferase family 92 protein;Glycosyltransferase family 92 protein F13G3.3	F13G3.3	Caenorhabditis elegans
172508	Chitin synthase chs-1	chs-1	Caenorhabditis elegans
172851	Chondroitin sulfate synthase sqv-5;Hexosyltransferase	sqv-5	Caenorhabditis elegans	temtamy preaxial brachydactyly syndrome

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