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 **226 - 250** of **449** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
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
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
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
308519	dpy-19 like C-mannosyltransferase 3	Dpy19l3
315496	dpy-19 like C-mannosyltransferase 1	Dpy19l1
297824	dpy-19 like 4	Dpy19l4
300461	dpy-19 like 2	Dpy19l2	spermatogenic failure 9
29640	dolichyl-phosphate mannosyltransferase subunit 2, regulatory	Dpm2	congenital disorder of glycosylation Iu
296394	dolichyl-phosphate mannosyltransferase subunit 1, catalytic	Dpm1	congenital disorder of glycosylation Ie congenital disorder of glycosylation type I
300668	dolichyl-phosphate N-acetylglucosaminephosphotransferase 1	Dpagt1	congenital disorder of glycosylation Ij congenital myasthenic syndrome 13
81654	dihydrolipoamide S-acetyltransferase	Dlat	lactic acidosis pyruvate decarboxylase deficiency
171408	dicarbonyl and L-xylulose reductase	Dcxr	pentosuria
252900	diacylglycerol O-acyltransferase 2	Dgat2	chronic kidney disease metabolic dysfunction-associated steatotic liver disease premature menopause steatotic liver disease
361272	dehydrogenase E1 and transketolase domain containing 1	Dhtkd1	2-aminoadipic 2-oxoadipic aciduria Charcot-Marie-Tooth disease axonal type 2Q
290741	dCMP deaminase	Dctd
299691	cryptochrome circadian regulator 1	Cry1	delayed sleep phase syndrome