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 **7751 - 7775** of **9988** in total

« First

‹ Prev

…

307

308

309

310

311

312

313

314

315

…

Next ›

Last »
Gene ID	Gene Name	Gene Symbol	Organism ▼	Disease Ontology
128368	olfactory receptor family 10 subfamily Z member 1	OR10Z1	Homo sapiens (human)
66002	cytochrome P450 family 4 subfamily F member 12	CYP4F12	Homo sapiens (human)
162387	major facilitator superfamily domain containing 6 like	MFSD6L	Homo sapiens (human)
5701	proteasome 26S subunit, ATPase 2	PSMC2	Homo sapiens (human)
84617	tubulin beta 6 class V	TUBB6	Homo sapiens (human)
340596	LHFPL tetraspan subfamily member 1	LHFPL1	Homo sapiens (human)
2028	glutamyl aminopeptidase	ENPEP	Homo sapiens (human)
64921	CAS1 domain containing 1	CASD1	Homo sapiens (human)
5100	protocadherin 8	PCDH8	Homo sapiens (human)
2201	fibrillin 2	FBN2	Homo sapiens (human)
79871	RNA polymerase II associated protein 2	RPAP2	Homo sapiens (human)
23198	proteasome activator subunit 4	PSME4	Homo sapiens (human)
7094	talin 1	TLN1	Homo sapiens (human)
120071	LARGE xylosyl- and glucuronyltransferase 2	LARGE2 Aliases: FLJ35207 PP5656	Homo sapiens (human)	Duchenne muscular dystrophy acute myocardial infarction 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 cancer congenital muscular dystrophy coronary thrombosis distal myopathy embryoma facioscapulohumeral muscular dystrophy limb-girdle muscular dystrophy muscular dystrophy myocardial infarction myofibrillar myopathy 1 myofibrillar myopathy 3 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 prostate cancer prostate carcinoma rippling muscle disease 2 silent myocardial infarction transitional cell carcinoma
4160	melanocortin 4 receptor	MC4R	Homo sapiens (human)
23632	carbonic anhydrase 14	CA14	Homo sapiens (human)
1066	carboxylesterase 1	CES1	Homo sapiens (human)
55565	zinc finger protein 821	ZNF821	Homo sapiens (human)
3915	laminin subunit gamma 1	LAMC1	Homo sapiens (human)
283149	BCL9 like	BCL9L	Homo sapiens (human)
100287932	translocase of inner mitochondrial membrane 23	TIMM23	Homo sapiens (human)
390181	olfactory receptor family 5 subfamily AK member 2	OR5AK2	Homo sapiens (human)
254225	ring finger protein 169	RNF169	Homo sapiens (human)
3125	major histocompatibility complex, class II, DR beta 3	HLA-DRB3	Homo sapiens (human)
4686	nuclear cap binding protein subunit 1	NCBP1	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

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

International Collaboration

Acknowledgements