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 **9301 - 9325** of **9988** in total

« First

‹ Prev

…

369

370

371

372

373

374

375

376

377

…

Next ›

Last »
Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
284759	signal regulatory protein beta 2	SIRPB2	Homo sapiens (human)
284996	ring finger protein 149	RNF149	Homo sapiens (human)
285093	receptor transporter protein 5 (putative)	RTP5	Homo sapiens (human)
285172	hyccin PI4KA lipid kinase complex subunit 2	HYCC2	Homo sapiens (human)
285175	unc-80 homolog, NALCN channel complex subunit	UNC80	Homo sapiens (human)
285190	RANBP2 like and GRIP domain containing 4	RGPD4	Homo sapiens (human)
285195	solute carrier family 9 member A9	SLC9A9	Homo sapiens (human)
285203	EGF domain specific O-linked N-acetylglucosamine transferase	EOGT Aliases: AER61 AER61 glycosyltransferase FLJ33770	Homo sapiens (human)	Adams-Oliver syndrome Clouston syndrome alopecia arteriovenous malformation autosomal recessive polycystic kidney disease cataract clubfoot communicating hydrocephalus epilepsy hydrocephalus hypertropia intellectual disability learning disability leukopenia mechanical strabismus microphthalmia obstructive hydrocephalus ophthalmoplegia periventricular leukomalacia polycystic kidney disease 4 portal hypertension primary pulmonary hypertension senile degeneration of brain strabismus tetralogy of Fallot thrombocytopenia visual epilepsy
285220	EPH receptor A6	EPHA6	Homo sapiens (human)
285242	5-hydroxytryptamine receptor 3E	HTR3E	Homo sapiens (human)
285313	immunoglobulin superfamily member 10	IGSF10	Homo sapiens (human)
285362	sulfatase modifying factor 1	SUMF1 Aliases: FGE UNQ3037	Homo sapiens (human)	Balo concentric sclerosis Laron syndrome X-linked chondrodysplasia punctata 1 X-linked ichthyosis achondroplasia adrenoleukodystrophy autosomal dominant cerebellar ataxia autosomal dominant chondrodysplasia punctata autosomal recessive spinocerebellar ataxia 16 blindness breast cancer breast carcinoma cancer cataract central nervous system disease cerebral degeneration chondrodysplasia punctata chronic obstructive pulmonary disease communicating hydrocephalus cystic fibrosis embryoma epilepsy hydrocephalus ichthyosis inherited metabolic disorder intellectual disability learning disability lysosomal storage disease metachromatic leukodystrophy microcephaly mucopolysaccharidosis I mucopolysaccharidosis II mucopolysaccharidosis III mucopolysaccharidosis IV mucopolysaccharidosis IVA mucopolysaccharidosis Ih mucopolysaccharidosis VI mucopolysaccharidosis type IIIA mucopolysaccharidosis mucosulfatidosis multiple sclerosis narcolepsy obstructive hydrocephalus optic atrophy recurrent corneal erosion retinal degeneration rhizomelic chondrodysplasia punctata type 1 rhizomelic chondrodysplasia punctata type 2 rhizomelic chondrodysplasia punctata type 3 schizophrenia senile degeneration of brain sensorineural hearing loss visual epilepsy
285368	proline rich transmembrane protein 3	PRRT3	Homo sapiens (human)
285386	tumor protein p63 regulated 1	TPRG1	Homo sapiens (human)
285489	docking protein 7	DOK7	Homo sapiens (human)
285527	FRY like transcription coactivator	FRYL	Homo sapiens (human)
285533	ring finger protein 175	RNF175	Homo sapiens (human)
285550	family with sequence similarity 200 member B	FAM200B	Homo sapiens (human)
285555	sperm tail PG-rich repeat containing 2	STPG2	Homo sapiens (human)
285590	SH3 and PX domains 2B	SH3PXD2B	Homo sapiens (human)
285605	DTW domain containing 2	DTWD2	Homo sapiens (human)
285659	olfactory receptor family 2 subfamily V member 2	OR2V2	Homo sapiens (human)
285704	repulsive guidance molecule BMP co-receptor b	RGMB Aliases: DRAGON FLJ90406	Homo sapiens (human)	allergic asthma asthma atrial fibrillation brain stem infarction breast cancer cancer cerebral artery occlusion cerebral infarction cerebrovascular disease colorectal cancer colorectal carcinoma embryoma hemochromatosis type 2 hemochromatosis type 2A hemochromatosis hepatocellular carcinoma intrinsic asthma large intestine cancer liver cancer lung cancer lung non-small cell carcinoma middle cerebral artery infarction multiple sclerosis prostate cancer prostate carcinoma rheumatoid arthritis
285761	discoidin, CUB and LCCL domain containing 1	DCBLD1	Homo sapiens (human)
285800	proline rich 18	PRR18	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