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 **201 - 225** of **449** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▼
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
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
302489	heparan sulfate 6-O-sulfotransferase 2	Hs6st2	Paganini-Miozzo syndrome
25594	protein phosphatase 1 catalytic subunit beta	Ppp1cb	Noonan syndrome-like disorder with loose anagen hair 2 cancer
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
293722	beta-1,3-glucuronyltransferase 3	B3gat3	Larsen-like syndrome B3GAT3 type
364682	NHL repeat containing E3 ubiquitin protein ligase 1	Nhlrc1	Lafora disease
114005	EPM2A glucan phosphatase, laforin	Epm2a	Lafora disease progressive myoclonus epilepsy
25623	glycogen synthase 2	Gys2	Lafora disease glycogen storage disease
690987	glycogen synthase 1	Gys1	Lafora disease cardiovascular system disease
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
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
293504	quinolinate phosphoribosyltransferase	Qprt	Huntington's disease
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
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
25556	interleukin 1 receptor-like 1	Il1rl1	Hantavirus hemorrhagic fever with renal syndrome Human papillomavirus infectious disease acute myocardial infarction asthma bacterial pneumonia chronic obstructive pulmonary disease coronary artery disease hemolytic-uremic syndrome idiopathic pulmonary fibrosis paracoccidioidomycosis rhinitis tongue squamous cell carcinoma
24465	hypoxanthine phosphoribosyltransferase 1	Hprt1	HRPT-related hyperuricemia Lesch-Nyhan syndrome hepatocellular carcinoma
81528	8-oxoguanine DNA glycosylase	Ogg1	Graves' disease Parkinson's disease angiomyolipoma basal cell carcinoma breast cancer cataract cholangiocarcinoma coronary artery disease gestational diabetes head and neck squamous cell carcinoma hepatitis hypertension middle cerebral artery infarction ovarian cancer pancreatic cancer pre-eclampsia primary open angle glaucoma progressive supranuclear palsy prostate cancer pterygium renal cell carcinoma senile cataract status epilepticus transient cerebral ischemia transitional cell carcinoma type 2 diabetes mellitus
24651	pyruvate kinase L/R	Pklr	Gaucher's disease congenital nonspherocytic hemolytic anemia disease of metabolism hyperglycemia malaria metabolic dysfunction-associated steatotic liver disease pyruvate kinase deficiency of red cells type 2 diabetes mellitus
114711	glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase	Gne	GNE myopathy sialuria
362520	fukutin	Fktn	Fukuyama congenital muscular dystrophy Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M dilated cardiomyopathy 1B dilated cardiomyopathy 1X muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B4 muscular dystrophy
315165	alpha-N-acetylgalactosaminidase	Naga	Fabry disease Kanzaki disease Schindler disease type 1 angiokeratoma neuroaxonal dystrophy
298690	Beta-1,3-galactosyltransferase 6	B3galt6	Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome spondyloepimetaphyseal dysplasia with joint laxity type 1
364675	beta-1,4-galactosyltransferase 7	B4galt7	Ehlers-Danlos syndrome spondylodysplastic type 1 Ehlers-Danlos syndrome
691394	carbohydrate sulfotransferase 14	Chst14	Ehlers-Danlos syndrome musculocontractural type 1

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