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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 .

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 "polysaccharide binding"

Displaying entries **1 - 25** of **2452** in total

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Gene ID	Gene Name	Gene Symbol ▲	Organism	Disease Ontology
4707278	endo-1,4-beta-mannosidase, putative	ACLA_044470	Aspergillus clavatus NRRL 1
4708945	endoglucanase, putative	ACLA_059790	Aspergillus clavatus NRRL 1
4706008	cellobiohydrolase, putative	ACLA_062560	Aspergillus clavatus NRRL 1
4699868	glycosyl hydrolase family 7 protein	ACLA_085260	Aspergillus clavatus NRRL 1
3513161	endoglucanase, putative	AFUA_2G14540	Aspergillus fumigatus Af293
3505986	cellobiohydrolase, putative	AFUA_3G01910	Aspergillus fumigatus Af293
3509671	endoglucanase, putative	AFUA_4G07850	Aspergillus fumigatus Af293
3508349	1,4-beta-D-glucan-cellobiohydrolyase, putative	AFUA_6G11610	Aspergillus fumigatus Af293
3504738	acetyl xylan esterase, putative	AFUA_8G06570	Aspergillus fumigatus Af293
3504710	endoglucanase, putative	AFUA_8G06830	Aspergillus fumigatus Af293
3504904	endo-1,4-beta-mannosidase, putative	AFUA_8G07030	Aspergillus fumigatus Af293
178	amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase	AGL Aliases: GDE glycogen debranching enzyme glycogen storage disease type III	Homo sapiens (human)	Duchenne muscular dystrophy Laron syndrome achondroplasia acute promyelocytic leukemia atrichia with papular lesions 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 bladder carcinoma cancer cardiomyopathy colon cancer colon carcinoma colonic benign neoplasm colorectal cancer congenital generalized lipodystrophy type 1 congenital generalized lipodystrophy type 2 congenital generalized lipodystrophy type 3 congenital generalized lipodystrophy type 4 congenital muscular dystrophy cystinuria disease of metabolism distal myopathy endomyocardial fibrosis facioscapulohumeral muscular dystrophy familial hyperlipidemia familial partial lipodystrophy familial periodic paralysis galactosemia giardiasis glucosephosphate dehydrogenase deficiency glycogen storage disease II glycogen storage disease III glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease hepatitis C hypertrophic cardiomyopathy hypoglycemia isolated elevated serum creatine phosphokinase levels kidney failure large intestine cancer limb-girdle muscular dystrophy lipoatrophic diabetes mellitus lipodystrophy liver cirrhosis lung cancer lung non-small cell carcinoma muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 myopathy nodular nonsuppurative panniculitis 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 oculopharyngeal muscular dystrophy panniculitis primary immunodeficiency disease rippling muscle disease 2 uremia urinary bladder cancer
2876273	protein cbhB	ANIA_00494	Aspergillus nidulans FGSC A4
2876816	hypothetical protein	ANIA_01041	Aspergillus nidulans FGSC A4
2875535	endoglucanase GH61 family protein	ANIA_01602	Aspergillus nidulans FGSC A4
2875438	hypothetical protein	ANIA_02388	Aspergillus nidulans FGSC A4
2874014	hypothetical protein	ANIA_03046	Aspergillus nidulans FGSC A4
2873281	hypothetical protein	ANIA_03860	Aspergillus nidulans FGSC A4
2871574	protein cbhC	ANIA_05282	Aspergillus nidulans FGSC A4
2871754	hypothetical protein	ANIA_05463	Aspergillus nidulans FGSC A4
2871327	hypothetical protein	ANIA_06428	Aspergillus nidulans FGSC A4
2867914	protein manF	ANIA_09276	Aspergillus nidulans FGSC A4
3684123	hypothetical protein	ANIA_09524	Aspergillus nidulans FGSC A4
5999830	hypothetical protein	AO090010000746	Aspergillus oryzae RIB40
839596	5'-AMP-activated protein kinase-like protein	AT1G27070	Arabidopsis thaliana (thale cress)

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