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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 **26 - 50** of **423164** in total

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Gene ID ▲	Gene Name	Gene Symbol	Organism	Disease Ontology
38	acetyl-CoA acetyltransferase 1	ACAT1 Aliases: THIL acetoacetyl Coenzyme A thiolase	Homo sapiens (human)	beta-ketothiolase deficiency carbohydrate metabolic disorder
39	acetyl-CoA acetyltransferase 2	ACAT2 Aliases: Acetyl-CoA acetyltransferase, cytosolic acetoacetyl Coenzyme A thiolase	Homo sapiens (human)	coronary artery disease
40	acid sensing ion channel subunit 2	ASIC2	Homo sapiens (human)
41	acid sensing ion channel subunit 1	ASIC1	Homo sapiens (human)
43	acetylcholinesterase (Yt blood group)	ACHE Aliases: Yt blood group	Homo sapiens (human)	Alzheimer's disease cannabis dependence drug dependence epilepsy heroin dependence myasthenia gravis subacute delirium
47	ATP citrate lyase	ACLY Aliases: ACL ATP citrate synthase ATPCL CLATP	Homo sapiens (human)
48	aconitase 1	ACO1 Aliases: IREBP IRP1 aconitate hydratase, cytoplasmic cytosplasmic aconitase soluble aconitase	Homo sapiens (human)
49	acrosin	ACR	Homo sapiens (human)	spermatogenic failure 87
50	aconitase 2	ACO2 Aliases: ACONM aconitate hydratase, mitochondrial mitochondrial aconitase	Homo sapiens (human)	infantile cerebellar-retinal degeneration optic atrophy 9
51	acyl-CoA oxidase 1	ACOX1 Aliases: PALMCOX palmitoyl-CoA oxidase	Homo sapiens (human)	Mitchell syndrome peroxisomal acyl-CoA oxidase deficiency
53	acid phosphatase 2, lysosomal	ACP2 Aliases: LAP lysosomal acid phosphatase	Homo sapiens (human)
54	acid phosphatase 5, tartrate resistant	ACP5 Aliases: HPAP TRAP TRAcP human purple acid phosphatase tartrate-resistant acid phosphatase	Homo sapiens (human)	spondylometaphyseal dysplasia
55	acid phosphatase 3	ACP3 Aliases: ACP-3 PAP TM-PAP prostatic acid phosphatase	Homo sapiens (human)	prostate cancer
56	acrosomal vesicle protein 1	ACRV1	Homo sapiens (human)
58	actin alpha 1, skeletal muscle	ACTA1 Aliases: NEM3 nemaline myopathy type 3	Homo sapiens (human)	congenital myopathy 2B congenital myopathy 2C nemaline myopathy 3
59	actin alpha 2, smooth muscle	ACTA2 Aliases: ACTSA	Homo sapiens (human)	Moyamoya disease thoracic aortic aneurysm
60	actin beta	ACTB Aliases: β-actin	Homo sapiens (human)	Baraitser-Winter syndrome 1 thrombocytopenia
70	actin alpha cardiac muscle 1	ACTC1 Aliases: CMD1R	Homo sapiens (human)	atrial heart septal defect 5 dilated cardiomyopathy 1R dilated cardiomyopathy hypertrophic cardiomyopathy 11
71	actin gamma 1	ACTG1	Homo sapiens (human)	Baraitser-Winter syndrome 2 autosomal dominant nonsyndromic deafness 20
81	actinin alpha 4	ACTN4	Homo sapiens (human)	focal segmental glomerulosclerosis 1 focal segmental glomerulosclerosis
86	actin like 6A	ACTL6A	Homo sapiens (human)
87	actinin alpha 1	ACTN1	Homo sapiens (human)	platelet-type bleeding disorder 15
88	actinin alpha 2	ACTN2	Homo sapiens (human)	arrhythmogenic right ventricular cardiomyopathy congenital myopathy 8 dilated cardiomyopathy 1AA
90	activin A receptor type 1	ACVR1	Homo sapiens (human)	exfoliation syndrome fibrodysplasia ossificans progressiva primary angle-closure glaucoma primary open angle glaucoma
91	activin A receptor type 1B	ACVR1B	Homo sapiens (human)	lung non-small cell carcinoma lung small cell carcinoma malignant mesothelioma pancreatic cancer stomach cancer

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