GlyCosmos Portal

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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	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 **9001 - 9025** of **9988** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
2131	exostosin glycosyltransferase 1	EXT1 Aliases: Glucuronosyl-N-acetylglucosaminyl-proteoglycan 4-alpha-N- acetylglucosaminyltransferase N-acetylglucosaminyl-proteoglycan 4-beta-glucuronosyltransferase ttv	Homo sapiens (human)	Alzheimer's disease Cenani-Lenz syndactyly syndrome Cornelia de Lange syndrome 4 Cornelia de Lange syndrome Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Laron syndrome Legg-Calve-Perthes disease Lennox-Gastaut syndrome Leri-Weill dyschondrosteosis Maffucci syndrome Ollier disease Pick's disease Reye syndrome Ritter's disease Werner syndrome achondroplasia acute lymphoblastic leukemia adenocarcinoma adenoma adult acute lymphocytic leukemia anaplastic astrocytoma antisocial personality disorder arthritis arthropathy autism spectrum disorder autistic disorder autoimmune disease autoimmune lymphoproliferative syndrome bone cancer bone disease bone osteosarcoma breast cancer breast carcinoma cancer cartilage disease central nervous system cancer cerebral degeneration cervix uteri carcinoma in situ cherubism childhood acute lymphocytic leukemia childhood cerebral astrocytoma childhood leukemia chondroblastoma chondroma chondrosarcoma cleidocranial dysplasia clubfoot conduct disorder connective tissue disease cranial nerve disease cranial nerve palsy cribriform carcinoma cryoglobulinemia diabetes mellitus disease of mental health embryoma endometrial cancer endometrial carcinoma epilepsy exostosis familial hypercholesterolemia familial nephrotic syndrome fibrillary astrocytoma fibromyalgia frontotemporal dementia gallbladder disease gemistocytic astrocytoma gliosarcoma granular cell carcinoma head and neck squamous cell carcinoma hepatitis A hepatitis B hepatitis C hepatitis E hepatitis hepatocellular carcinoma hereditary multiple exostoses high grade glioma humeroradial synostosis hydrocephalus hyperostosis hypogonadism hypogonadotropic hypogonadism 7 with or without anosmia immune system disease intellectual disability juvenile myoclonic epilepsy juvenile pilocytic astrocytoma learning disability leukemia lipoid nephrosis liver cancer liver disease lupus nephritis malignant astrocytoma membranous glomerulonephritis metachondromatosis microcephaly mixed glioma mucopolysaccharidosis III mucopolysaccharidosis type IIIA multiple myeloma myositis nephrotic syndrome osteoarthritis osteonecrosis osteopoikilosis osteoporosis osteosarcoma periarthritis personality disorder pilocytic astrocytoma progeria protoplasmic astrocytoma psychotic disorder radioulnar synostosis rectal benign neoplasm rectum adenocarcinoma rectum cancer rheumatoid arthritis schizophrenia scoliosis spinal cord disease subependymal giant cell astrocytoma tendinitis thrombophilia trichorhinophalangeal syndrome type II tubular adenocarcinoma type 2 diabetes mellitus urinary tract obstruction uterine corpus cancer vasculitis vesicoureteral reflux visual epilepsy
2130	EWS RNA binding protein 1	EWSR1	Homo sapiens (human)
2125	envoplakin	EVPL	Homo sapiens (human)
2124	ecotropic viral integration site 2B	EVI2B	Homo sapiens (human)
2123	ecotropic viral integration site 2A	EVI2A	Homo sapiens (human)
2122	MDS1 and EVI1 complex locus	MECOM	Homo sapiens (human)
2115	ETS variant transcription factor 1	ETV1	Homo sapiens (human)
2109	electron transfer flavoprotein subunit beta	ETFB	Homo sapiens (human)
2107	eukaryotic translation termination factor 1	ETF1	Homo sapiens (human)
2099	estrogen receptor 1	ESR1	Homo sapiens (human)
2091	fibrillarin	FBL	Homo sapiens (human)
2086	endogenous retrovirus group 3 member 1, envelope	ERV3-1	Homo sapiens (human)
2081	endoplasmic reticulum to nucleus signaling 1	ERN1 Aliases: IRE1 IRE1P Serine/threonine-protein kinase/endoribonuclease IRE1 inositol-requiring enzyme 1	Homo sapiens (human)
2074	ERCC excision repair 6, chromatin remodeling factor	ERCC6	Homo sapiens (human)
2073	ERCC excision repair 5, endonuclease	ERCC5	Homo sapiens (human)
2070	EYA transcriptional coactivator and phosphatase 4	EYA4	Homo sapiens (human)
2069	epiregulin	EREG	Homo sapiens (human)
2066	erb-b2 receptor tyrosine kinase 4	ERBB4	Homo sapiens (human)
2065	erb-b2 receptor tyrosine kinase 3	ERBB3	Homo sapiens (human)
2064	erb-b2 receptor tyrosine kinase 2	ERBB2	Homo sapiens (human)
2060	epidermal growth factor receptor pathway substrate 15	EPS15	Homo sapiens (human)
2059	EGFR pathway substrate 8, signaling adaptor	EPS8	Homo sapiens (human)
2058	glutamyl-prolyl-tRNA synthetase 1	EPRS1	Homo sapiens (human)
2057	erythropoietin receptor	EPOR	Homo sapiens (human)
2056	erythropoietin	EPO	Homo sapiens (human)

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