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 ▲
287545	sterile alpha and TIR motif containing 1	Sarm1	amyotrophic lateral sclerosis neurodegenerative disease
140808	mannosidase, endo-alpha	Manea	anxiety disorder cocaine dependence panic disorder
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
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
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
25438	enolase 3	Eno3	aortic valve stenosis
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
113901	chitinase, acidic	Chia	asthma cryptococcosis silicosis sinusitis
362809	prostaglandin E synthase 3	Ptges3	atherosclerosis breast cancer oligodendroglioma
361450	uronyl-2-sulfotransferase	Ust	attention deficit hyperactivity disorder
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
299907	exostosin glycosyltransferase 1	Ext1	autism spectrum disorder chondrosarcoma hereditary multiple exostoses
65044	core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1	C1galt1	autoimmune disease of blood
24191	aldolase, fructose-bisphosphate C	Aldoc	autoimmune disease of the nervous system borna disease hepatocellular carcinoma
363464	phosphatidylinositol glycan anchor biosynthesis, class A	Piga	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
24788	sorbitol dehydrogenase	Sord	autosomal recessive distal hereditary motor neuronopathy 8 cataract diabetic neuropathy obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy
64445	ST3 beta-galactoside alpha-2,3-sialyltransferase 3	St3gal3	autosomal recessive intellectual developmental disorder 12 developmental and epileptic encephalopathy 15
290501	transmembrane O-mannosyltransferase targeting cadherins 4	Tmtc4	autosomal recessive nonsyndromic deafness
310864	mannosidase beta	Manba	beta-mannosidosis
170587	citrate synthase	Cs	bipolar disorder congestive heart failure dilated cardiomyopathy hyperthyroidism hypertrophic cardiomyopathy hypothyroidism limb ischemia myocardial infarction retinal degeneration
83507	poly (ADP-ribose) glycohydrolase	Parg	borna disease brain infarction stress-induced childhood-onset neurodegeneration with variable ataxia and seizures
79255	activating transcription factor 4	Atf4	borna disease prostate carcinoma pulmonary venoocclusive disease
81829	malate dehydrogenase 2	Mdh2	brain ischemia congestive heart failure developmental and epileptic encephalopathy 51 myocardial infarction

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