GlyCosmos Portal

Table Filtering

Gene ID

Gene Name

Gene Symbol

Organism

Taxonomy ID

Disease Ontology

Disease Ontology ID

Gene Ontology

Gene Ontology ID

Display
results per page.

Clear

Submissions

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 **551 - 575** of **422592** in total

« First

‹ Prev

…

19

20

21

22

23

24

25

26

27

…

Next ›

Last »
Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
1120	choline kinase beta	CHKB Aliases: CHETK	Homo sapiens (human)	Balo concentric sclerosis Bell's palsy Duchenne muscular dystrophy X-linked dilated cardiomyopathy adrenoleukodystrophy 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 bronchus cancer bronchus carcinoma campomelic dysplasia central nervous system disease centronuclear myopathy congenital merosin-deficient muscular dystrophy 1A congenital muscular dystrophy 1B congenital muscular dystrophy due to LMNA mutation congenital muscular dystrophy due to integrin alpha-7 deficiency congenital muscular dystrophy congenital myopathy 1A congenital myopathy 4A congenital structural myopathy craniometaphyseal dysplasia cytochrome-c oxidase deficiency disease developmental coordination disorder dilated cardiomyopathy 1AA dilated cardiomyopathy 1B dilated cardiomyopathy 1BB dilated cardiomyopathy 1C dilated cardiomyopathy 1CC dilated cardiomyopathy 1D dilated cardiomyopathy 1DD dilated cardiomyopathy 1E dilated cardiomyopathy 1EE dilated cardiomyopathy 1FF dilated cardiomyopathy 1G dilated cardiomyopathy 1GG dilated cardiomyopathy 1H dilated cardiomyopathy 1HH dilated cardiomyopathy 1I dilated cardiomyopathy 1II dilated cardiomyopathy 1JJ dilated cardiomyopathy 1K dilated cardiomyopathy 1KK dilated cardiomyopathy 1L dilated cardiomyopathy 1M dilated cardiomyopathy 1NN dilated cardiomyopathy 1O dilated cardiomyopathy 1P dilated cardiomyopathy 1Q dilated cardiomyopathy 1R dilated cardiomyopathy 1S dilated cardiomyopathy 1T dilated cardiomyopathy 1U dilated cardiomyopathy 1V dilated cardiomyopathy 1W dilated cardiomyopathy 1X dilated cardiomyopathy 1Y dilated cardiomyopathy 1Z dilated cardiomyopathy 2A dilated cardiomyopathy 2B dilated cardiomyopathy distal myopathy epilepsy facial nerve disease facial paralysis facioscapulohumeral muscular dystrophy inherited metabolic disorder intellectual disability isolated elevated serum creatine phosphokinase levels limb-girdle muscular dystrophy lung benign neoplasm lung cancer lung carcinoma megaconial type congenital muscular dystrophy microcephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy-dystroglycanopathy type B6 muscular dystrophy myofibrillar myopathy 1 myofibrillar myopathy 3 narcolepsy nemaline myopathy 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 recurrent hypersomnia restless legs syndrome rigid spine muscular dystrophy 1 rippling muscle disease 2
1121	CHM Rab escort protein	CHM	Homo sapiens (human)
1122	CHM like Rab escort protein	CHML	Homo sapiens (human)
1128	cholinergic receptor muscarinic 1	CHRM1	Homo sapiens (human)
1129	cholinergic receptor muscarinic 2	CHRM2	Homo sapiens (human)
1130	lysosomal trafficking regulator	LYST	Homo sapiens (human)
1131	cholinergic receptor muscarinic 3	CHRM3	Homo sapiens (human)
1132	cholinergic receptor muscarinic 4	CHRM4	Homo sapiens (human)
1133	cholinergic receptor muscarinic 5	CHRM5	Homo sapiens (human)
1134	cholinergic receptor nicotinic alpha 1 subunit	CHRNA1	Homo sapiens (human)
1135	cholinergic receptor nicotinic alpha 2 subunit	CHRNA2	Homo sapiens (human)
1136	cholinergic receptor nicotinic alpha 3 subunit	CHRNA3	Homo sapiens (human)
1137	cholinergic receptor nicotinic alpha 4 subunit	CHRNA4	Homo sapiens (human)
1138	cholinergic receptor nicotinic alpha 5 subunit	CHRNA5	Homo sapiens (human)
1139	cholinergic receptor nicotinic alpha 7 subunit	CHRNA7	Homo sapiens (human)
1140	cholinergic receptor nicotinic beta 1 subunit	CHRNB1	Homo sapiens (human)
1141	cholinergic receptor nicotinic beta 2 subunit	CHRNB2	Homo sapiens (human)
1142	cholinergic receptor nicotinic beta 3 subunit	CHRNB3	Homo sapiens (human)
1143	cholinergic receptor nicotinic beta 4 subunit	CHRNB4	Homo sapiens (human)
1144	cholinergic receptor nicotinic delta subunit	CHRND	Homo sapiens (human)
1145	cholinergic receptor nicotinic epsilon subunit	CHRNE	Homo sapiens (human)
1146	cholinergic receptor nicotinic gamma subunit	CHRNG	Homo sapiens (human)
1147	component of inhibitor of nuclear factor kappa B kinase complex	CHUK	Homo sapiens (human)
1159	creatine kinase, mitochondrial 1B	CKMT1B	Homo sapiens (human)
1173	adaptor related protein complex 2 subunit mu 1	AP2M1	Homo sapiens (human)

Download data in CSV format Download data in TSV format Download data in JSON format

Table Filtering

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements