GlyCosmos Portal

Rattus norvegicus (Norway rat)

Summary

Taxonomy ID: 10116
PubChem Taxonomy: 10116

Genes (449) Glycans (773) Glycoproteins (2935) Lectins (166) Pathways (1070)

Displaying entries **301 - 325** of **449** in total

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Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
286971	fucosyltransferase 11	Fut11	stomach cancer
497619	fucosyltransferase 10	Fut10
81919	fucosyltransferase 1	Fut1
292485	alpha-L-fucosidase 2	Fuca2
24375	alpha-L-fucosidase 1	Fuca1	diabetes mellitus diabetic retinopathy fucosidosis type 1 diabetes mellitus type 2 diabetes mellitus
362520	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
308390	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
114508	fructose-bisphosphatase 2	Fbp2
24362	fructose-bisphosphatase 1	Fbp1	fructose-1,6-bisphosphatase deficiency
140868	fatty acid binding protein 5	Fabp5	prostate cancer psoriasis
56819	exostosin-like glycosyltransferase 3	Extl3	hereditary multiple exostoses
310803	exostosin-like glycosyltransferase 2	Extl2
313610	exostosin-like glycosyltransferase 1	Extl1	hereditary multiple exostoses
311215	exostosin glycosyltransferase 2	Ext2	hereditary multiple exostoses
299907	exostosin glycosyltransferase 1	Ext1	autism spectrum disorder chondrosarcoma hereditary multiple exostoses
313729	ERBB receptor feedback inhibitor 1	Errfi1	endometrial cancer osteoarthritis
114005	EPM2A glucan phosphatase, laforin	Epm2a	Lafora disease progressive myoclonus epilepsy
494219	EGF domain specific O-linked N-acetylglucosamine transferase	Eogt	Adams-Oliver syndrome
85496	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
25438	enolase 3	Eno3	aortic valve stenosis
24334	enolase 2	Eno2	Parkinsonism brain disease breast carcinoma hypertension migraine without aura neuroendocrine carcinoma prostate cancer toxic shock syndrome urinary bladder cancer visual epilepsy
24333	enolase 1	Eno1	Alzheimer's disease hypertension
297824	dpy-19 like 4	Dpy19l4
308519	dpy-19 like C-mannosyltransferase 3	Dpy19l3
300461	dpy-19 like 2	Dpy19l2	spermatogenic failure 9

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