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 **476 - 500** of **662** in total

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Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
17425	forkhead box K1	Foxk1
246179	fukutin	Fktn	Fukuyama congenital muscular dystrophy Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M dilated cardiomyopathy 1B dilated cardiomyopathy 1X muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B4 muscular dystrophy
243853	fukutin related protein	Fkrp	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2I congenital muscular dystrophy-dystroglycanopathy type A5 dilated cardiomyopathy limb-girdle muscular dystrophy muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy
75578	FGGY carbohydrate kinase domain containing	Fggy
234730	fucose kinase	Fcsk
14120	fructose bisphosphatase 2	Fbp2
14121	fructose bisphosphatase 1	Fbp1	fructose-1,6-bisphosphatase deficiency
16592	fatty acid binding protein 5, epidermal	Fabp5	prostate cancer psoriasis
54616	exostosin-like glycosyltransferase 3	Extl3	hereditary multiple exostoses
58193	exostosin-like glycosyltransferase 2	Extl2
56219	exostosin-like glycosyltransferase 1	Extl1	hereditary multiple exostoses
14043	exostosin glycosyltransferase 2	Ext2	hereditary multiple exostoses
14042	exostosin glycosyltransferase 1	Ext1	autism spectrum disorder chondrosarcoma hereditary multiple exostoses
74155	ERBB receptor feedback inhibitor 1	Errfi1	endometrial cancer osteoarthritis
77781	EPM2A interacting protein 1	Epm2aip1
13853	epilepsy, progressive myoclonic epilepsy, type 2 gene alpha	Epm2a	Lafora disease progressive myoclonus epilepsy
101351	EGF domain specific O-linked N-acetylglucosamine transferase	Eogt	Adams-Oliver syndrome
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
226265	enolase 4	Eno4
13808	enolase 3, beta muscle	Eno3	aortic valve stenosis
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
433182	enolase 1B, retrotransposed	Eno1b	Alzheimer's disease hypertension
13806	enolase 1, alpha non-neuron	Eno1	Alzheimer's disease hypertension
217364	endo-beta-N-acetylglucosaminidase	Engase
66967	ER degradation enhancer, mannosidase alpha-like 3	Edem3	congenital disorder of glycosylation type II

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