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 **326 - 350** of **449** in total

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Gene ID	Gene Name ▲	Gene Symbol	Disease Ontology
310864	mannosidase beta	Manba	beta-mannosidosis
499751	mannosidase, alpha, class 1B, member 1	Man1b1	Rafiq syndrome
25478	mannosidase, alpha, class 2A, member 1	Man2a1	congenital dyserythropoietic anemia systemic lupus erythematosus
246136	mannosidase, alpha, class 2C, member 1	Man2c1
140808	mannosidase, endo-alpha	Manea	anxiety disorder cocaine dependence panic disorder
78947	mannosyl-oligosaccharide glucosidase	Mogs	congenital disorder of glycosylation type IIb
683630	methionine adenosyltransferase 2 non-catalytic beta subunit	Mat2b
246233	mono-ADP ribosylhydrolase 1	Macrod1
170841	mutY DNA glycosylase	Mutyh	familial adenomatous polyposis 2 familial adenomatous polyposis stomach cancer stomach carcinoma
117185	neuraminidase 3	Neu3
297508	nicotinamide phosphoribosyltransferase	Nampt	carotid artery disease coronary artery disease kidney failure metabolic dysfunction-associated steatotic liver disease middle cerebral artery infarction obesity periodontitis psoriasis pulmonary hypertension transient cerebral ischemia 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
361274	nudix hydrolase 5	Nudt5
25231	one cut homeobox 1	Onecut1
360975	oxoglutarate dehydrogenase	Ogdh	Yoon-Bellen neurodevelopmental syndrome oxoglutarate dehydrogenase deficiency
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
63840	period circadian regulator 2	Per2	advanced sleep phase syndrome 1 advanced sleep phase syndrome cocaine dependence
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
363464	phosphatidylinositol glycan anchor biosynthesis, class A	Piga	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
315807	phosphatidylinositol glycan anchor biosynthesis, class B	Pigb	developmental and epileptic encephalopathy 80 sleeping sickness
79112	phosphatidylinositol glycan anchor biosynthesis, class M	Pigm
366478	phosphatidylinositol glycan anchor biosynthesis, class V	Pigv	hyperphosphatasia with impaired intellectual development syndrome 1
303872	phosphatidylinositol glycan anchor biosynthesis, class Z	Pigz	cancer
170911	phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit alpha	Pik3ca	CLOVES syndrome Cowden syndrome 5 autosomal recessive polycystic kidney disease breast angiosarcoma breast cancer cerebral cavernous malformation colon adenocarcinoma colorectal cancer colorectal carcinoma cutaneous Paget's disease epidermal nevus esophageal cancer estrogen-receptor positive breast cancer hepatocellular carcinoma lung cancer ovarian cancer rectal benign neoplasm seborrheic keratosis stomach cancer
362282	phosphoenolpyruvate carboxykinase 1	Pck1	Alzheimer's disease metabolic dysfunction-associated steatohepatitis type 2 diabetes mellitus

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