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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 **7501 - 7525** of **9988** in total

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Gene ID	Gene Name	Gene Symbol ▼	Organism	Disease Ontology
83939	eukaryotic translation initiation factor 2A	EIF2A	Homo sapiens (human)
10209	eukaryotic translation initiation factor 1	EIF1	Homo sapiens (human)
10919	euchromatic histone lysine methyltransferase 2	EHMT2	Homo sapiens (human)
79813	euchromatic histone lysine methyltransferase 1	EHMT1	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
254102	EH domain binding protein 1 like 1	EHBP1L1	Homo sapiens (human)
23301	EH domain binding protein 1	EHBP1	Homo sapiens (human)
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)
133584	EGF like, fibronectin type III and laminin G domains	EGFLAM	Homo sapiens (human)
80864	EGF like domain multiple 8	EGFL8	Homo sapiens (human)
51162	EGF like domain multiple 7	EGFL7	Homo sapiens (human)
25975	EGF like domain multiple 6	EGFL6	Homo sapiens (human)
1950	epidermal growth factor	EGF	Homo sapiens (human)
9343	elongation factor Tu GTP binding domain containing 2	EFTUD2	Homo sapiens (human)
22979	EFR3 homolog B	EFR3B	Homo sapiens (human)
23167	EFR3 homolog A	EFR3A	Homo sapiens (human)
1949	ephrin B3	EFNB3	Homo sapiens (human)
1948	ephrin B2	EFNB2	Homo sapiens (human)
1947	ephrin B1	EFNB1	Homo sapiens (human)
1946	ephrin A5	EFNA5 Aliases: AF1 EPH-related receptor tyrosine kinase ligand 7 LERK7	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 Ambras type hypertrichosis universalis congenita IGSF1 deficiency syndrome Norum disease Pick's disease Reye syndrome Tangier disease abdominal aortic aneurysm abetalipoproteinemia acquired immunodeficiency syndrome acute lymphoblastic leukemia acute myeloid leukemia adult medulloblastoma amyotrophic lateral sclerosis anencephaly arteriosclerotic cardiovascular disease atherosclerosis atrial fibrillation blindness breast cancer breast carcinoma bulimia nervosa cancer cardiovascular system disease cataract cerebral degeneration cerebral infarction cerebral palsy cerebrovascular disease childhood medulloblastoma chondrosarcoma choreaacanthocytosis colitis conduct disorder congenital hypothyroidism congenital nongoitrous hypothyroidism 1 congenital nongoitrous hypothyroidism 2 congenital nongoitrous hypothyroidism 3 congenital nongoitrous hypothyroidism 4 congenital nongoitrous hypothyroidism 5 congenital nongoitrous hypothyroidism 6 coronary artery disease cystic fibrosis diffuse large B-cell lymphoma embryoma enophthalmos familial hypobetalipoproteinemia 1 gastric ulcer gastroenteritis heart disease hemiplegia hepatocellular carcinoma human immunodeficiency virus infectious disease hypobetalipoproteinemia hypolipoproteinemia hypothyroidism ileitis ileocolitis infertility inflammatory bowel disease 1 inflammatory bowel disease liver cancer lymphoblastic lymphoma medulloblastoma medullomyoblastoma melanotic medulloblastoma myxedema nicotine dependence nutmeg liver obsessive-compulsive disorder obsolete exophthalmos orbital disease peripheral vascular disease progressive muscular atrophy prostate cancer prostate carcinoma schizophrenia sclerocornea senile cataract spastic diplegia spastic monoplegia spastic quadriplegic cerebral palsy synovitis systemic lupus erythematosus tenosynovitis thrombocytopenia ulcerative colitis
1945	ephrin A4	EFNA4	Homo sapiens (human)
1944	ephrin A3	EFNA3	Homo sapiens (human)

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