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 **101 - 125** of **449** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
171393	calsyntenin 3	Clstn3
290637	collagen beta(1-O)galactosyltransferase 1	Colgalt1	brain small vessel disease 3
289081	collagen beta(1-O)galactosyltransferase 2	Colgalt2
24267	catechol-O-methyltransferase	Comt	Parkinsonism alcohol dependence alcohol use disorder amphetamine abuse attention deficit hyperactivity disorder autism spectrum disorder bipolar disorder breast cancer bulimia nervosa cannabis abuse cannabis dependence cocaine dependence cognitive disorder drug dependence endometrial cancer eumycotic mycetoma fibromyalgia heroin dependence hypertension intermittent explosive disorder leiomyoma lung cancer morphine dependence neonatal abstinence syndrome nicotine dependence obesity obsessive-compulsive disorder opiate dependence ovarian cancer pathological gambling polycystic ovary syndrome pre-eclampsia prostate cancer psoriasis renal cell carcinoma schizophrenia uremia urinary bladder cancer vitiligo withdrawal disorder
498332	coenzyme Q2, polyprenyltransferase	Coq2	coenzyme Q10 deficiency disease glucose intolerance multiple system atrophy nephrotic syndrome primary coenzyme Q10 deficiency 1
29309	coenzyme Q3 methyltransferase	Coq3
25757	carnitine palmitoyltransferase 1A	Cpt1a	alcoholic hepatitis carnitine palmitoyltransferase I deficiency end stage renal disease lipid metabolism disorder lymphangioleiomyomatosis metabolic dysfunction-associated steatohepatitis obesity type 2 diabetes mellitus
25620	cAMP responsive element modulator	Crem	transient cerebral ischemia
310615	CREB regulated transcription coactivator 2	Crtc2	type 2 diabetes mellitus
299691	cryptochrome circadian regulator 1	Cry1	delayed sleep phase syndrome
170587	citrate synthase	Cs	bipolar disorder congestive heart failure dilated cardiomyopathy hyperthyroidism hypertrophic cardiomyopathy hypothyroidism limb ischemia myocardial infarction retinal degeneration
306375	chondroitin sulfate N-acetylgalactosaminyltransferase 1	Csgalnact1
297554	chondroitin sulfate N-acetylgalactosaminyltransferase 2	Csgalnact2
81652	chitobiase	Ctbs
290741	dCMP deaminase	Dctd
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
81654	dihydrolipoamide S-acetyltransferase	Dlat	lactic acidosis pyruvate decarboxylase deficiency
171047	2'-deoxynucleoside 5'-phosphate N-hydrolase 1	Dnph1
300668	dolichyl-phosphate N-acetylglucosaminephosphotransferase 1	Dpagt1	congenital disorder of glycosylation Ij congenital myasthenic syndrome 13
296394	dolichyl-phosphate mannosyltransferase subunit 1, catalytic	Dpm1	congenital disorder of glycosylation Ie congenital disorder of glycosylation type I
29640	dolichyl-phosphate mannosyltransferase subunit 2, regulatory	Dpm2	congenital disorder of glycosylation Iu
315496	dpy-19 like C-mannosyltransferase 1	Dpy19l1
300461	dpy-19 like 2	Dpy19l2	spermatogenic failure 9

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