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 **151 - 175** of **449** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▼
65044	core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1	C1galt1	autoimmune disease of blood
299907	exostosin glycosyltransferase 1	Ext1	autism spectrum disorder chondrosarcoma hereditary multiple exostoses
114002	N-deacetylase and N-sulfotransferase 2	Ndst2	autism spectrum disorder azoospermia intellectual disability
295430	N-deacetylase and N-sulfotransferase 3	Ndst3	autism spectrum disorder azoospermia intellectual disability
362035	N-deacetylase and N-sulfotransferase 4	Ndst4	autism spectrum disorder azoospermia intellectual disability
361450	uronyl-2-sulfotransferase	Ust	attention deficit hyperactivity disorder
362809	prostaglandin E synthase 3	Ptges3	atherosclerosis breast cancer oligodendroglioma
113901	chitinase, acidic	Chia	asthma cryptococcosis silicosis sinusitis
24536	leptin receptor	Lepr	arteriosclerosis chronic kidney disease chronic obstructive pulmonary disease congestive heart failure coronary artery disease diastolic heart failure dilated cardiomyopathy glucose intolerance hepatocellular carcinoma hepatocellular clear cell carcinoma human immunodeficiency virus infectious disease hyperglycemia hyperinsulinism hypertension metabolic dysfunction-associated steatohepatitis metabolic dysfunction-associated steatotic liver disease obesity obstructive sleep apnea osteoporosis pancreatitis pre-eclampsia primary biliary cholangitis proteinuria renal fibrosis short bowel syndrome sleep apnea type 2 diabetes mellitus
25438	enolase 3	Eno3	aortic valve stenosis
26295	O-linked N-acetylglucosamine (GlcNAc) transferase	Ogt	aortic valve stenosis congestive heart failure diabetes mellitus non-syndromic X-linked intellectual disability 106 type 2 diabetes mellitus
24925	adrenoceptor beta 1	Adrb1	aortic valve stenosis chronic obstructive pulmonary disease congestive heart failure cystic fibrosis dilated cardiomyopathy hyperglycemia hypertension low tension glaucoma myocardial infarction nephrosclerosis obstructive sleep apnea periodontitis renovascular hypertension type 1 diabetes mellitus
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
140808	mannosidase, endo-alpha	Manea	anxiety disorder cocaine dependence panic disorder
287545	sterile alpha and TIR motif containing 1	Sarm1	amyotrophic lateral sclerosis neurodegenerative disease
24401	glutamic-oxaloacetic transaminase 1	Got1	amyloidosis amyotrophic lateral sclerosis cardiomyopathy pancreatic ductal adenocarcinoma transient cerebral ischemia
24192	aldo-keto reductase family 1 member B1	Akr1b1	allergic disease arteriosclerosis cataract diabetic neuropathy diabetic retinopathy galactosemia hepatocellular carcinoma hyperglycemia hypokalemia stomach cancer type 2 diabetes mellitus
301595	UDP glucuronosyltransferase family 1 member A8	Ugt1a8	alcoholic pancreatitis cholangiocarcinoma pancreatic cancer
154516	UDP glucuronosyltransferase 1 family, polypeptide A7C	Ugt1a7c	alcoholic pancreatitis cholangiocarcinoma pancreatic cancer type 2 diabetes mellitus
252917	nuclear receptor subfamily 1, group D, member 1	Nr1d1	alcoholic liver cirrhosis brain small vessel disease hyperthyroidism hypothyroidism portal hypertension type 2 diabetes mellitus
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
192280	protein phosphatase 1, regulatory subunit 3B	Ppp1r3b	alcohol use disorder
309513	protein phosphatase 1, regulatory subunit 3C	Ppp1r3c	alcohol use disorder type 2 diabetes mellitus
25197	ST6 beta-galactoside alpha-2,6-sialyltransferase 1	St6gal1	alcohol use disorder high grade glioma
24212	ATPase Na+/K+ transporting subunit alpha 2	Atp1a2	alcohol use disorder alternating hemiplegia of childhood benign neonatal seizures developmental and epileptic encephalopathy 98 epilepsy familial hemiplegic migraine 2 familial hemiplegic migraine hyperhomocysteinemia hypertension migraine with aura nervous system disease

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