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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 **826 - 850** of **9988** in total

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Gene ID	Gene Name ▲	Gene Symbol	Organism	Disease Ontology
2048	EPH receptor B2	EPHB2	Homo sapiens (human)
2049	EPH receptor B3	EPHB3	Homo sapiens (human)
2050	EPH receptor B4	EPHB4	Homo sapiens (human)
2051	EPH receptor B6	EPHB6	Homo sapiens (human)
7957	EPM2A glucan phosphatase, laforin	EPM2A Aliases: LD LDE	Homo sapiens (human)	Alzheimer's disease Balo concentric sclerosis Dravet syndrome Lafora disease MERRF syndrome Rett syndrome Unverricht-Lundborg syndrome adrenoleukodystrophy adult lymphoma agnosia alexia apraxia benign epilepsy with centrotemporal spikes blepharospasm blindness cancer central nervous system disease central nervous system lymphoma cerebral degeneration childhood lymphoma cystinuria dementia dentatorubral-pallidoluysian atrophy depressive disorder dyslexia dysthymic disorder early myoclonic encephalopathy embryoma endometrial carcinoma epilepsy focal hand dystonia galactosemia glucosephosphate dehydrogenase deficiency glycogen storage disease IXa glycogen storage disease IXb glycogen storage disease IXc glycogen storage disease IXd glycogen storage disease Ia glycogen storage disease intellectual disability learning disability lymphoma major depressive disorder melancholic depression narcolepsy neurodegenerative disease neuronal ceroid lipofuscinosis 10 neuronal ceroid lipofuscinosis 11 neuronal ceroid lipofuscinosis 13 neuronal ceroid lipofuscinosis 1 neuronal ceroid lipofuscinosis 2 neuronal ceroid lipofuscinosis 3 neuronal ceroid lipofuscinosis 4 neuronal ceroid lipofuscinosis 5 neuronal ceroid lipofuscinosis 6A neuronal ceroid lipofuscinosis 6B neuronal ceroid lipofuscinosis 7 neuronal ceroid lipofuscinosis 8 northern epilepsy variant neuronal ceroid lipofuscinosis 8 neuronal ceroid lipofuscinosis 9 neuronal ceroid lipofuscinosis neurotic disorder non-syndromic X-linked intellectual disability obsolete Dravet syndrome obsolete infantile epileptic encephalopathy obsolete melancholia obsolete ymphosarcoma photosensitive epilepsy photosensitivity disease progressive myoclonus epilepsy 1A progressive myoclonus epilepsy 4 progressive myoclonus epilepsy psychotic disorder schizoaffective disorder schizophrenia schizophreniform disorder status epilepticus
9852	EPM2A interacting protein 1	EPM2AIP1	Homo sapiens (human)
64787	EPS8 signaling adaptor L2	EPS8L2	Homo sapiens (human)
9695	ER degradation enhancing alpha-mannosidase like protein 1	EDEM1 Aliases: EDEM KIAA0212	Homo sapiens (human)	cystic fibrosis depressive disorder hepatitis C major depressive disorder melancholic depression melanoma neurotic disorder obsolete melancholia skin melanoma
55741	ER degradation enhancing alpha-mannosidase like protein 2	EDEM2 Aliases: FLJ10783 bA4204.1	Homo sapiens (human)	Alzheimer's disease 10 Alzheimer's disease 11 Alzheimer's disease 12 Alzheimer's disease 13 Alzheimer's disease 14 Alzheimer's disease 15 Alzheimer's disease 1 Alzheimer's disease 2 Alzheimer's disease 5 Alzheimer's disease 6 Alzheimer's disease 7 Alzheimer's disease 8 Alzheimer's disease Pick's disease Reye syndrome cerebral degeneration leiomyoma myofibroma schizophrenia uterine fibroid
80267	ER degradation enhancing alpha-mannosidase like protein 3	EDEM3	Homo sapiens (human)	congenital disorder of glycosylation type II hepatitis C prostate cancer prostate carcinoma
10613	ER lipid raft associated 1	ERLIN1	Homo sapiens (human)
11160	ER lipid raft associated 2	ERLIN2	Homo sapiens (human)
23065	ER membrane protein complex subunit 1	EMC1	Homo sapiens (human)
284361	ER membrane protein complex subunit 10	EMC10	Homo sapiens (human)
9694	ER membrane protein complex subunit 2	EMC2	Homo sapiens (human)
56851	ER membrane protein complex subunit 7	EMC7	Homo sapiens (human)
10328	ER membrane protein complex subunit 8	EMC8	Homo sapiens (human)
54206	ERBB receptor feedback inhibitor 1	ERRFI1	Homo sapiens (human)	endometrial cancer osteoarthritis
2073	ERCC excision repair 5, endonuclease	ERCC5	Homo sapiens (human)
375748	ERCC excision repair 6 like 2	ERCC6L2	Homo sapiens (human)
2074	ERCC excision repair 6, chromatin remodeling factor	ERCC6	Homo sapiens (human)
51290	ERGIC and golgi 2	ERGIC2	Homo sapiens (human)
51614	ERGIC and golgi 3	ERGIC3	Homo sapiens (human)
112479	ERI1 exoribonuclease family member 2	ERI2	Homo sapiens (human)
109504726	ERV3-1-ZNF117 readthrough	ERV3-1-ZNF117	Homo sapiens (human)

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