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 **421676 - 421700** of **422592** in total

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Gene ID ▼	Gene Name	Gene Symbol	Organism	Disease Ontology
1983	eukaryotic translation initiation factor 5	EIF5	Homo sapiens (human)
1982	eukaryotic translation initiation factor 4 gamma 2	EIF4G2	Homo sapiens (human)
1981	eukaryotic translation initiation factor 4 gamma 1	EIF4G1	Homo sapiens (human)
1978	eukaryotic translation initiation factor 4E binding protein 1	EIF4EBP1	Homo sapiens (human)
1977	eukaryotic translation initiation factor 4E	EIF4E	Homo sapiens (human)
1975	eukaryotic translation initiation factor 4B	EIF4B	Homo sapiens (human)
1973	eukaryotic translation initiation factor 4A1	EIF4A1	Homo sapiens (human)
1969	EPH receptor A2	EPHA2	Homo sapiens (human)
1968	eukaryotic translation initiation factor 2 subunit gamma	EIF2S3 Aliases: EIF2 EIF2gamma eukaryotic translation initiation factor 2G	Homo sapiens (human)
1967	eukaryotic translation initiation factor 2B subunit alpha	EIF2B1	Homo sapiens (human)
1965	eukaryotic translation initiation factor 2 subunit alpha	EIF2S1	Homo sapiens (human)
1962	enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase	EHHADH	Homo sapiens (human)	D-bifunctional protein deficiency Fanconi renotubular syndrome 3 Fanconi syndrome Laron syndrome Zollinger-Ellison syndrome achondroplasia amyloidosis bipolar disorder cancer carnitine palmitoyltransferase II deficiency cystinosis cystinuria cytochrome-c oxidase deficiency disease familial hyperinsulinemic hypoglycemia 1 familial hyperinsulinemic hypoglycemia 2 galactosemia gallbladder disease 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 hepatocellular carcinoma hyperinsulinemic hypoglycemia hyperinsulinism liver cancer liver disease mitochondrial trifunctional protein deficiency osteomalacia prostate cancer prostate carcinoma proteinuria rickets spondyloepimetaphyseal dysplasia, Sponastrime type substance abuse substance-related disorder tuberculosis
1960	early growth response 3	EGR3	Homo sapiens (human)
1959	early growth response 2	EGR2	Homo sapiens (human)
1958	early growth response 1	EGR1	Homo sapiens (human)
1956	epidermal growth factor receptor	EGFR	Homo sapiens (human)
1955	multiple EGF like domains 9	MEGF9	Homo sapiens (human)
1954	multiple EGF like domains 8	MEGF8	Homo sapiens (human)
1953	multiple EGF like domains 6	MEGF6	Homo sapiens (human)
1952	cadherin EGF LAG seven-pass G-type receptor 2	CELSR2	Homo sapiens (human)
1951	cadherin EGF LAG seven-pass G-type receptor 3	CELSR3	Homo sapiens (human)
1950	epidermal growth factor	EGF	Homo sapiens (human)
1949	ephrin B3	EFNB3	Homo sapiens (human)
1948	ephrin B2	EFNB2	Homo sapiens (human)
1947	ephrin B1	EFNB1	Homo sapiens (human)

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