GlyCosmos Portal

Mus musculus (house mouse)

Summary

Taxonomy ID: 10090
PubChem Taxonomy: 10090

Genes (662) Glycans (1270) Glycoproteins (13000) Lectins (276) Pathways (1335)

Displaying entries **151 - 175** of **662** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
235339	dihydrolipoamide S-acetyltransferase	Dlat	lactic acidosis pyruvate decarboxylase deficiency
381101	2'-deoxynucleoside 5'-phosphate N-hydrolase 1	Dnph1
13478	dolichyl-phosphate N-acetylglucosaminephosphotransferase 1	Dpagt1	congenital disorder of glycosylation Ij congenital myasthenic syndrome 13
13480	dolichyl-phosphate mannosyltransferase subunit 1, catalytic	Dpm1	congenital disorder of glycosylation Ie congenital disorder of glycosylation type I
13481	dolichyl-phosphate mannosyltransferase subunit 2, regulatory	Dpm2	congenital disorder of glycosylation Iu congenital disorder of glycosylation type I
244745	dpy-19 like C-mannosyltransferase 1	Dpy19l1
320752	dpy-19 like 2	Dpy19l2	spermatogenic failure 9
233115	dpy-19 like C-mannosyltransferase 3	Dpy19l3
381510	dpy-19 like 4	Dpy19l4
26903	dysferlin	Dysf	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	cystic fibrosis
108687	ER degradation enhancer, mannosidase alpha-like 2	Edem2
66967	ER degradation enhancer, mannosidase alpha-like 3	Edem3	congenital disorder of glycosylation type II
217364	endo-beta-N-acetylglucosaminidase	Engase
13806	enolase 1, alpha non-neuron	Eno1	Alzheimer's disease hypertension
433182	enolase 1B, retrotransposed	Eno1b	Alzheimer's disease hypertension
13807	enolase 2, gamma neuronal	Eno2	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	aortic valve stenosis
226265	enolase 4	Eno4
18605	ectonucleotide pyrophosphatase/phosphodiesterase 1	Enpp1	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	Adams-Oliver syndrome
13853	epilepsy, progressive myoclonic epilepsy, type 2 gene alpha	Epm2a	Lafora disease progressive myoclonus epilepsy
77781	EPM2A interacting protein 1	Epm2aip1
74155	ERBB receptor feedback inhibitor 1	Errfi1	endometrial cancer osteoarthritis
14042	exostosin glycosyltransferase 1	Ext1	autism spectrum disorder chondrosarcoma hereditary multiple exostoses

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