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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 **2601 - 2625** of **393515** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
188207	Uncharacterized protein	T07A5.1	Caenorhabditis elegans	Fukuyama congenital muscular dystrophy Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M dilated cardiomyopathy 1B dilated cardiomyopathy 1X muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B4 muscular dystrophy
189104	Uncharacterized protein	W02B3.4	Caenorhabditis elegans	Fukuyama congenital muscular dystrophy Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M dilated cardiomyopathy 1B dilated cardiomyopathy 1X muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B4 muscular dystrophy
189173	Putative alpha-L-fucosidase	W03G11.3	Caenorhabditis elegans	diabetes mellitus diabetic retinopathy fucosidosis type 1 diabetes mellitus type 2 diabetes mellitus
189361	Putative galactoside 2-alpha-L-fucosyltransferase svh-11	svh-11	Caenorhabditis elegans
189753	Beta-1,3-galactosyltransferase bre-2;Hexosyltransferase	bre-2	Caenorhabditis elegans
190099	Xylosyltransferase sqv-6;protein xylosyltransferase	sqv-6	Caenorhabditis elegans	Desbuquois dysplasia kidney disease polycystic kidney disease pseudoxanthoma elasticum type 1 diabetes mellitus
190436	UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase	algn-7	Caenorhabditis elegans	congenital disorder of glycosylation Ij congenital myasthenic syndrome 13
190668	Beta-1,4-N-acetylgalactosaminyltransferase bre-4	bre-4	Caenorhabditis elegans	IgA glomerulonephritis congenital disorder of glycosylation type IId congenital disorder of glycosylation endocrine system disease multiple sclerosis
191306	Glycosyltransferase family 92 protein ZK381.2	ZK381.2	Caenorhabditis elegans
191628	C-mannosyltransferase dpy-19	dpy-19	Caenorhabditis elegans	spermatogenic failure 9
192134	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	B3GNT6 Aliases: B3Gn-T6 core 3 synthase	Homo sapiens (human)	cancer colon carcinoma colorectal cancer colorectal carcinoma embryoma familial adenomatous polyposis 1 familial adenomatous polyposis islet cell tumor large intestine cancer pancreatic cancer pancreatic carcinoma prostate cancer prostate carcinoma
192193	ER degradation enhancer, mannosidase alpha-like 1	Edem1	Mus musculus (house mouse)	cystic fibrosis
192280	protein phosphatase 1, regulatory subunit 3B	Ppp1r3b	Rattus norvegicus (Norway rat)	alcohol use disorder
192281	2'-5' oligoadenylate synthetase 1A	Oas1a	Rattus norvegicus (Norway rat)	primary immunodeficiency disease
192309	triosephosphate isomerase 1a	tpi1a	Danio rerio (zebrafish)	cancer carbohydrate metabolic disorder neurodegenerative disease ocular hypertension triosephosphate isomerase deficiency
192315	UDP-glucuronate decarboxylase 1	uxs1	Danio rerio (zebrafish)
192334	beta-1,3-glucuronyltransferase 3 (glucuronosyltransferase I)	b3gat3	Danio rerio (zebrafish)	Larsen-like syndrome B3GAT3 type
192361	protein phosphatase 1, regulatory (inhibitor) subunit 2	Ppp1r2	Rattus norvegicus (Norway rat)
195646	heparan sulfate (glucosamine) 3-O-sulfotransferase 2	Hs3st2	Mus musculus (house mouse)	colon cancer lung cancer lung non-small cell carcinoma pancreatic cancer
196051	phospholipid phosphatase 4	PLPP4 Aliases: DPPL2 diacylglycerol pyrophosphate phosphatase-like 2	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 Pick's disease Reye syndrome breast cancer bronchus cancer bronchus carcinoma cerebral degeneration lung cancer lung carcinoma lung squamous cell carcinoma prostate cancer prostate carcinoma
197021	lactase like	LCTL Aliases: FLJ33279 KL lactase phlorizin hydrolase KLG KLPH gammaklotho klotho gamma	Homo sapiens (human)	arthritis arthropathy kidney disease osteoarthritis
197257	lactate dehydrogenase D	LDHD	Homo sapiens (human)	aniridia chromophobe renal cell carcinoma clear cell renal cell carcinoma collecting duct carcinoma intellectual disability learning disability microcephaly nonpapillary renal cell carcinoma papillary renal cell carcinoma renal carcinoma renal cell carcinoma sarcomatoid renal cell carcinoma
197258	fucose kinase	FCSK Aliases: FLJ39408 L-fucose kinase	Homo sapiens (human)	congenital disorder of glycosylation congenital nystagmus dissociated nystagmus epilepsy esophagitis gastroesophageal reflux disease hypertropia intellectual disability learning disability mechanical strabismus ophthalmoplegia optic atrophy pathologic nystagmus peptic esophagitis spontaneous ocular nystagmus strabismus visual epilepsy
197322	acyl-CoA synthetase family member 3	ACSF3 Aliases: malonyl-CoA synthetase	Homo sapiens (human)	B-cell lymphoma adult lymphoma amnestic disorder brain disease central nervous system lymphoma childhood lymphoma combined malonic and methylmalonic acidemia diarrhea disease of metabolism dystonia hypoglycemia inherited metabolic disorder lymphoma methylmalonic acidemia microcephaly migraine obsolete ymphosarcoma retrograde amnesia
199857	ALG14 UDP-N-acetylglucosaminyltransferase subunit	ALG14 Aliases: MGC19780	Homo sapiens (human)	Bell's palsy agnosia clubfoot congenital myasthenic syndrome 15 congenital myasthenic syndrome congenital ptosis developmental coordination disorder facial nerve disease facial paralysis familial periodic paralysis idiopathic scoliosis intellectual disability isolated elevated serum creatine phosphokinase levels learning disability myopathy ptosis scoliosis syndromic X-linked intellectual disability 94

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