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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	July 8, 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 **151 - 175** of **662** in total

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Gene ID	Gene Name	Gene Symbol ▲	Organism	Disease Ontology
235339	dihydrolipoamide S-acetyltransferase	Dlat	Mus musculus (house mouse)	lactic acidosis pyruvate decarboxylase deficiency
381101	2'-deoxynucleoside 5'-phosphate N-hydrolase 1	Dnph1	Mus musculus (house mouse)
13478	dolichyl-phosphate N-acetylglucosaminephosphotransferase 1	Dpagt1	Mus musculus (house mouse)	congenital disorder of glycosylation Ij congenital myasthenic syndrome 13
13480	dolichyl-phosphate mannosyltransferase subunit 1, catalytic	Dpm1	Mus musculus (house mouse)	congenital disorder of glycosylation Ie congenital disorder of glycosylation type I
13481	dolichyl-phosphate mannosyltransferase subunit 2, regulatory	Dpm2	Mus musculus (house mouse)	congenital disorder of glycosylation Iu congenital disorder of glycosylation type I
244745	dpy-19 like C-mannosyltransferase 1	Dpy19l1	Mus musculus (house mouse)
320752	dpy-19 like 2	Dpy19l2	Mus musculus (house mouse)	spermatogenic failure 9
233115	dpy-19 like C-mannosyltransferase 3	Dpy19l3	Mus musculus (house mouse)
381510	dpy-19 like 4	Dpy19l4	Mus musculus (house mouse)
26903	dysferlin	Dysf	Mus musculus (house mouse)	Miyoshi muscular dystrophy 1 autosomal recessive limb-girdle muscular dystrophy type 2B distal myopathy with anterior tibial onset distal myopathy limb-girdle muscular dystrophy muscular dystrophy
192193	ER degradation enhancer, mannosidase alpha-like 1	Edem1	Mus musculus (house mouse)	cystic fibrosis
108687	ER degradation enhancer, mannosidase alpha-like 2	Edem2	Mus musculus (house mouse)
66967	ER degradation enhancer, mannosidase alpha-like 3	Edem3	Mus musculus (house mouse)	congenital disorder of glycosylation type II
217364	endo-beta-N-acetylglucosaminidase	Engase	Mus musculus (house mouse)
13806	enolase 1, alpha non-neuron	Eno1	Mus musculus (house mouse)	Alzheimer's disease hypertension
433182	enolase 1B, retrotransposed	Eno1b	Mus musculus (house mouse)	Alzheimer's disease hypertension
13807	enolase 2, gamma neuronal	Eno2	Mus musculus (house mouse)	Parkinsonism brain disease breast carcinoma hypertension migraine without aura neuroendocrine carcinoma prostate cancer toxic shock syndrome urinary bladder cancer visual epilepsy
13808	enolase 3, beta muscle	Eno3	Mus musculus (house mouse)	aortic valve stenosis
226265	enolase 4	Eno4	Mus musculus (house mouse)
18605	ectonucleotide pyrophosphatase/phosphodiesterase 1	Enpp1	Mus musculus (house mouse)	aortic valve disease 1 arterial calcification of infancy cardiovascular system disease end stage renal disease glioblastoma obesity ossification of the posterior longitudinal ligament of spine osteoarthritis otitis media pseudoxanthoma elasticum spondyloarthropathy tympanosclerosis type 2 diabetes mellitus
101351	EGF domain specific O-linked N-acetylglucosamine transferase	Eogt	Mus musculus (house mouse)	Adams-Oliver syndrome
13853	epilepsy, progressive myoclonic epilepsy, type 2 gene alpha	Epm2a	Mus musculus (house mouse)	Lafora disease progressive myoclonus epilepsy
77781	EPM2A interacting protein 1	Epm2aip1	Mus musculus (house mouse)
74155	ERBB receptor feedback inhibitor 1	Errfi1	Mus musculus (house mouse)	endometrial cancer osteoarthritis
14042	exostosin glycosyltransferase 1	Ext1	Mus musculus (house mouse)	autism spectrum disorder chondrosarcoma hereditary multiple exostoses

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