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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 **9176 - 9200** of **9988** in total

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Gene ID	Gene Name ▼	Gene Symbol	Organism	Disease Ontology
129080	EMI domain containing 1	EMID1	Homo sapiens (human)
400954	EMAP like 6	EML6	Homo sapiens (human)
27436	EMAP like 4	EML4	Homo sapiens (human)
256364	EMAP like 3	EML3	Homo sapiens (human)
79993	ELOVL fatty acid elongase 7	ELOVL7 Aliases: FLJ23563	Homo sapiens (human)	Parkinson's disease 19A Parkinson's disease 23 Parkinson's disease 4 Parkinson's disease adrenoleukodystrophy cancer hidradenitis suppurativa hidradenitis inflammatory bowel disease multiple system atrophy pompholyx prostate cancer prostate carcinoma
79071	ELOVL fatty acid elongase 6	ELOVL6 Aliases: FLJ23378 LCE MGC5487	Homo sapiens (human)	Fanconi anemia complementation group A Fanconi anemia Zollinger-Ellison syndrome accommodative esotropia acrodermatitis acute myeloid leukemia acute myocardial infarction allergic contact dermatitis amnestic disorder arteriolosclerosis arteriosclerosis arteriosclerotic cardiovascular disease atherosclerosis atopic dermatitis azoospermia bronchus cancer bronchus carcinoma cancer cone-rod dystrophy congestive heart failure coronary artery disease coronary thrombosis dermatitis diabetes mellitus disease of metabolism dissociative amnesia fundus albipunctatus hepatocellular carcinoma hyperinsulinism idiopathic interstitial pneumonia idiopathic pulmonary fibrosis liver cancer liver carcinoma lung benign neoplasm lung cancer lung carcinoma myocardial infarction nodular prostate obesity parapsoriasis postinflammatory pulmonary fibrosis prostatic adenoma psoriasis psoriatic arthritis pulmonary fibrosis pustulosis of palm and sole retinitis pigmentosa silent myocardial infarction steatotic liver disease type 2 diabetes mellitus
60481	ELOVL fatty acid elongase 5	ELOVL5 Aliases: HELO1 dJ483K16.1	Homo sapiens (human)	acute myocardial infarction autosomal dominant cerebellar ataxia cancer cardiac arrest cerebellar ataxia cerebellar disease colon cancer colonic benign neoplasm colorectal cancer colorectal carcinoma congenital nystagmus coronary thrombosis depressive disorder diabetes mellitus diabetic ketoacidosis dissociated nystagmus embryoma glaucoma glomerulonephritis hyperglycemia kidney disease large intestine cancer low tension glaucoma major depressive disorder melancholic depression myocardial infarction nephritis nephrosis obesity obsolete melancholia pathologic nystagmus primary open angle glaucoma prostate cancer prostate carcinoma pyoureter retinitis pigmentosa 25 schizophrenia silent myocardial infarction spinocerebellar ataxia type 1 spinocerebellar ataxia type 2 spinocerebellar ataxia type 38 spinocerebellar ataxia type 5 spinocerebellar ataxia type 6 spinocerebellar ataxia type 7 spontaneous ocular nystagmus steatotic liver disease type 2 diabetes mellitus
6785	ELOVL fatty acid elongase 4	ELOVL4 Aliases: CT118 cancer/testis antigen 118	Homo sapiens (human)	Kuhnt-Junius degeneration Leber congenital amaurosis Sjogren-Larsson syndrome Stargardt disease achromatopsia acquired color blindness acquired hyperkeratosis acute myocardial infarction age related macular degeneration alternating hemiplegia of childhood angioedema anhidrosis autonomic neuropathy autosomal dominant cerebellar ataxia autosomal recessive congenital ichthyosis 1 autosomal recessive congenital ichthyosis blindness blue color blindness cancer cardiac arrest central nervous system disease cerebellar ataxia cerebellar disease color blindness cone-rod dystrophy 2 cone-rod dystrophy 7 cone-rod dystrophy congenital nystagmus congenital stationary night blindness 1A congenital stationary night blindness corneal dystrophy coronary thrombosis degeneration of macula and posterior pole diabetes mellitus diabetic ketoacidosis dissociated nystagmus dry eye syndrome epilepsy erythrokeratodermia variabilis et progressiva 1 erythrokeratodermia variabilis eye disease fundus albipunctatus glycogen storage disease II granuloma annulare hepatocellular carcinoma hypertropia hypohidrosis ichthyosis inguinal hernia keratosis follicularis liver cancer locked-in syndrome macular degeneration mechanical strabismus mongolian spot myocardial infarction nervous system disease neurodegenerative disease night blindness obsolete congenital ichthyosiform erythroderma ophthalmoplegia pathologic nystagmus pseudoxanthoma elasticum quadriplegia red color blindness red-green color blindness retinitis pigmentosa 25 retinitis pigmentosa 30 retinitis pigmentosa silent myocardial infarction skin disease spinocerebellar ataxia type 34 spontaneous ocular nystagmus strabismus thrombocytopenia type 2 diabetes mellitus urticaria visual epilepsy xerophthalmia
83401	ELOVL fatty acid elongase 3	ELOVL3 Aliases: CIG-30	Homo sapiens (human)	amnestic disorder atopic dermatitis dermatitis diabetes mellitus diabetic ketoacidosis ichthyosis prostate cancer prostate carcinoma retrograde amnesia type 2 diabetes mellitus
54898	ELOVL fatty acid elongase 2	ELOVL2 Aliases: Ssc2	Homo sapiens (human)	acute chest syndrome acute myocardial infarction autism spectrum disorder autistic disorder central nervous system cancer coronary artery disease coronary thrombosis giant cell glioblastoma glioblastoma gliosarcoma hepatocellular carcinoma high grade glioma liver cancer melanoma mixed glioma myocardial infarction papillary adenocarcinoma papillary renal cell carcinoma silent myocardial infarction skin melanoma steatotic liver disease thyroid gland papillary carcinoma
64834	ELOVL fatty acid elongase 1	ELOVL1 Aliases: Ssc1	Homo sapiens (human)	Cauda equina syndrome acanthosis nigricans acrodermatitis adrenoleukodystrophy cancer dermatitis dry eye syndrome hyperglycemia neurogenic bladder obsolete asthenopia xerophthalmia
255520	ELMO domain containing 2	ELMOD2	Homo sapiens (human)
85403	ELL associated factor 1	EAF1	Homo sapiens (human)
26059	ELKS/RAB6-interacting/CAST family member 2	ERC2	Homo sapiens (human)
23085	ELKS/RAB6-interacting/CAST family member 1	ERC1	Homo sapiens (human)
254102	EH domain binding protein 1 like 1	EHBP1L1	Homo sapiens (human)
23301	EH domain binding protein 1	EHBP1	Homo sapiens (human)
2059	EGFR pathway substrate 8, signaling adaptor	EPS8	Homo sapiens (human)
133584	EGF like, fibronectin type III and laminin G domains	EGFLAM	Homo sapiens (human)
10085	EGF like repeats and discoidin domains 3	EDIL3	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)
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
30008	EGF containing fibulin extracellular matrix protein 2	EFEMP2	Homo sapiens (human)

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