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 **51 - 75** of **449** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▲
65248	protein kinase AMP-activated catalytic subunit alpha 1	Prkaa1	Huntington's disease Parkinson's disease breast cancer cholestasis colon cancer lung non-small cell carcinoma obesity type 2 diabetes mellitus
54315	uncoupling protein 2	Ucp2	Huntington's disease carotid artery disease congestive heart failure diabetic neuropathy end stage renal disease hypertension hypothyroidism metabolic dysfunction-associated steatotic liver disease obesity obstructive jaundice polycystic liver disease steatotic liver disease transient cerebral ischemia type 2 diabetes mellitus
293504	quinolinate phosphoribosyltransferase	Qprt	Huntington's disease
84020	potassium voltage-gated channel subfamily Q member 1	Kcnq1	Jervell-Lange Nielsen syndrome atrial fibrillation familial atrial fibrillation hypertension long QT syndrome 1 long QT syndrome seminoma short QT syndrome type 2 diabetes mellitus
25459	high mobility group box 1	Hmgb1	Kawasaki disease amyotrophic lateral sclerosis atherosclerosis brain infarction cerebral infarction colon adenocarcinoma congestive heart failure high grade glioma hydrocephalus middle cerebral artery infarction myocardial infarction obstructive jaundice periodontitis pulmonary hypertension sciatic neuropathy systemic scleroderma
690987	glycogen synthase 1	Gys1	Lafora disease cardiovascular system disease
25623	glycogen synthase 2	Gys2	Lafora disease glycogen storage disease
114005	EPM2A glucan phosphatase, laforin	Epm2a	Lafora disease progressive myoclonus epilepsy
364682	NHL repeat containing E3 ubiquitin protein ligase 1	Nhlrc1	Lafora disease
293722	beta-1,3-glucuronyltransferase 3	B3gat3	Larsen-like syndrome B3GAT3 type
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
25594	protein phosphatase 1 catalytic subunit beta	Ppp1cb	Noonan syndrome-like disorder with loose anagen hair 2 cancer
302489	heparan sulfate 6-O-sulfotransferase 2	Hs6st2	Paganini-Miozzo syndrome
292804	glucose-6-phosphate isomerase	Gpi	Parkinson's disease acute lymphoblastic leukemia acute myeloid leukemia congenital hemolytic anemia congenital nonspherocytic hemolytic anemia heart disease intellectual disability neuromuscular disease
25233	AKT serine/threonine kinase 2	Akt2	Parkinson's disease alcohol use disorder cancer colorectal cancer endometrial cancer hepatocellular carcinoma high grade glioma hypertension hypoglycemia hypoinsulinemic hypoglycemia with hemihypertrophy ischemia malignant astrocytoma obesity ovarian carcinoma polycystic ovary syndrome prostate adenocarcinoma prostate cancer prostate carcinoma type 2 diabetes mellitus
24644	phosphoglycerate kinase 1	Pgk1	Parkinson's disease cancer hemolytic anemia phosphoglycerate kinase 1 deficiency
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
50686	glycogen synthase kinase 3 alpha	Gsk3a	Parkinsonism amyotrophic lateral sclerosis
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
83535	potassium inwardly-rectifying channel, subfamily J, member 11	Kcnj11	Parkinsonism diabetes mellitus familial hyperinsulinemic hypoglycemia 2 hyperinsulinism hypertension maturity-onset diabetes of the young type 13 permanent neonatal diabetes mellitus prediabetes syndrome sciatic neuropathy status epilepticus type 2 diabetes mellitus visual epilepsy
689765	beta 3-glucosyltransferase	B3glct	Peters plus syndrome
24377	glucose-6-phosphate dehydrogenase	G6pd	Plasmodium falciparum malaria anemia cataract cerebrovascular disease cholestasis congenital hypothyroidism congenital nonspherocytic hemolytic anemia diabetes mellitus favism hemolytic anemia hepatic encephalopathy hepatocellular carcinoma hyperhomocysteinemia kidney disease malaria metabolic dysfunction-associated steatotic liver disease myocardial infarction neonatal jaundice obesity phenylketonuria renovascular hypertension transient cerebral ischemia type 1 diabetes mellitus type 2 diabetes mellitus
499751	mannosidase, alpha, class 1B, member 1	Man1b1	Rafiq syndrome
294673	hexosaminidase subunit beta	Hexb	Sandhoff disease lysosomal storage disease spinal muscular atrophy
24434	glucuronidase, beta	Gusb	Sly syndrome mucopolysaccharidosis peritonitis

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