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 **76 - 100** of **449** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
25668	CD38 molecule	Cd38	type 1 diabetes mellitus type 2 diabetes mellitus
25685	insulin-like growth factor binding protein 1	Igfbp1	breast cancer diabetic angiopathy
25694	hyaluronan synthase 2	Has2	diabetes insipidus middle cerebral artery infarction pulmonary hypertension
25703	retinol binding protein 4	Rbp4	acute pyelonephritis atherosclerosis cerebral infarction chronic kidney disease colon adenoma congestive heart failure coronary artery disease diabetic angiopathy diabetic retinopathy dilated cardiomyopathy essential hypertension familial hypercholesterolemia gallbladder cancer gestational diabetes hyperinsulinism hypertension liver cirrhosis myocardial infarction obesity pre-eclampsia proliferative diabetic retinopathy psoriasis severe pre-eclampsia systemic scleroderma type 2 diabetes mellitus
25737	proliferating cell nuclear antigen	Pcna	Lewy body dementia ataxia-telangiectasia-like disorder-2 brain ischemia hepatocellular carcinoma hypothyroidism invasive ductal carcinoma leiomyoma liver cancer mucositis nephroblastoma obstructive jaundice osteoporosis renal cell carcinoma sciatic neuropathy seminoma stomach cancer transient cerebral ischemia
25739	glycogen phosphorylase B	Pygb
25741	phosphofructokinase, liver type	Pfkl	disease of metabolism glycogen storage disease
25747	peroxisome proliferator activated receptor alpha	Ppara	Alzheimer's disease alcoholic hepatitis coronary artery disease cystic fibrosis hepatocellular carcinoma hydrocephalus hypertension hypertensive encephalopathy lipid metabolism disorder myocardial infarction obesity periodontitis schizophrenia steatotic liver disease
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
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
29260	toll-like receptor 4	Tlr4	Alzheimer's disease Behcet's disease Kawasaki disease acute kidney failure acute necrotizing pancreatitis allergic conjunctivitis allergic contact dermatitis allergic rhinitis ankylosing spondylitis anogenital venereal wart anterior uveitis arteriosclerosis arthritis asthma atopic dermatitis breast cancer carotid artery disease carotid stenosis cholesteatoma of middle ear cholesteatoma chronic obstructive pulmonary disease colitis collagen disease coronary artery disease cutaneous leishmaniasis cystic echinococcosis cystic fibrosis dermatomyositis diabetes mellitus diabetic neuropathy diabetic retinopathy dry eye syndrome end stage renal disease exfoliation syndrome eye disease familial mediterranean fever glucose metabolism disease hepatocellular carcinoma hepatorenal syndrome herpes simplex virus keratitis ileitis invasive aspergillosis keratitis kidney failure liver cirrhosis low tension glaucoma lung disease macular degeneration mastitis mastoiditis melanoma meningococcal meningitis metabolic dysfunction-associated steatotic liver disease multiple sclerosis myocardial infarction obesity otitis media pancreatitis perinatal necrotizing enterocolitis pleural tuberculosis pre-eclampsia primary immunodeficiency disease primary open angle glaucoma psoriasis pulmonary emphysema pulmonary tuberculosis pulpitis renal fibrosis respiratory allergy respiratory syncytial virus infectious disease sciatic neuropathy sinusitis suppurative otitis media temporal arteritis tympanosclerosis type 1 diabetes mellitus type 2 diabetes mellitus urinary tract infection uveitis vitiligo
29309	coenzyme Q3 methyltransferase	Coq3
29353	phosphorylase kinase catalytic subunit gamma 1	Phkg1
29484	solute carrier family 3 member 1	Slc3a1	cystinuria
29535	pancreatic and duodenal homeobox 1	Pdx1	acute necrotizing pancreatitis cerebral infarction diabetes mellitus diabetic retinopathy hyperglycemia maturity-onset diabetes of the young type 4 maturity-onset diabetes of the young obesity pancreatic agenesis placental insufficiency type 1 diabetes mellitus type 2 diabetes mellitus
29582	beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase	Mgat3
29595	5-hydroxytryptamine receptor 2A	Htr2a	Alzheimer's disease alcohol dependence alcohol use disorder alcoholic psychosis anorexia nervosa autism spectrum disorder bladder neck obstruction chronic obstructive pulmonary disease cocaine abuse cocaine dependence congenital diaphragmatic hernia congestive heart failure depressive disorder hyperglycemia hypertension inflammatory and toxic neuropathy major depressive disorder nicotine dependence non-alcoholic fatty liver obesity obsessive-compulsive disorder pancreatitis pathological gambling schizophrenia steatotic liver disease withdrawal disorder
29623	UDP-glucuronosyltransferase 2 family, member 37	Ugt2b37
29633	N-deacetylase and N-sulfotransferase 1	Ndst1	DiGeorge syndrome autism spectrum disorder autosomal recessive intellectual developmental disorder 46 azoospermia congenital diaphragmatic hernia intellectual disability newborn respiratory distress syndrome
29640	dolichyl-phosphate mannosyltransferase subunit 2, regulatory	Dpm2	congenital disorder of glycosylation Iu
29750	polypeptide N-acetylgalactosaminyltransferase 7	Galnt7
29758	ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 3	St6galnac3
50555	UDP glycosyltransferase 8	Ugt8
50567	solute carrier family 3 member 2	Slc3a2	adenoid cystic carcinoma lung adenocarcinoma lung non-small cell carcinoma lung pleomorphic carcinoma stomach carcinoma tongue squamous cell carcinoma transitional cell carcinoma
50622	solute carrier family 23 member 2	Slc23a2

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