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 ▲
300757	hexosaminidase subunit alpha	Hexa	Tay-Sachs disease
302499	C1GALT1-specific chaperone 1	C1galt1c1	Tn polyagglutination syndrome hemolytic-uremic syndrome
308390	fukutin related protein	Fkrp	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2I congenital muscular dystrophy-dystroglycanopathy type A5 dilated cardiomyopathy limb-girdle muscular dystrophy muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy
84430	protein-O-mannosyltransferase 1	Pomt1	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2K cardiomyopathy cleft lip congenital muscular dystrophy-dystroglycanopathy type A1 lissencephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy muscular dystrophy
688673	protein-O-mannosyltransferase 2	Pomt2	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy congenital muscular dystrophy-dystroglycanopathy type A2 lissencephaly muscular dystrophy-dystroglycanopathy type B2 muscular dystrophy-dystroglycanopathy muscular dystrophy
362567	protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)	Pomgnt1	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2O congenital muscular dystrophy-dystroglycanopathy type A3 lissencephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B3 muscular dystrophy retinitis pigmentosa
299841	ribitol xylosyltransferase 1	Rxylt1	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A10
293667	beta-1,4-glucuronyltransferase 1	B4gat1	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A13 muscular dystrophy-dystroglycanopathy type B1
360975	oxoglutarate dehydrogenase	Ogdh	Yoon-Bellen neurodevelopmental syndrome oxoglutarate dehydrogenase deficiency
89824	chitinase 3 like 1	Chi3l1	acute myeloid leukemia arteriosclerosis asthma bacterial meningitis breast cancer bronchopulmonary dysplasia chondrosarcoma chronic obstructive pulmonary disease colorectal carcinoma congestive heart failure coronary artery disease endometrial cancer glioblastoma hypertension lung non-small cell carcinoma melanoma multiple myeloma myocardial infarction ovarian cancer pre-eclampsia prostate carcinoma pulmonary fibrosis pulmonary sarcoidosis rheumatoid arthritis schizophrenia small cell carcinoma systemic scleroderma temporal arteritis type 1 diabetes mellitus type 2 diabetes mellitus
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
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
292072	adenine phosphoribosyl transferase	Aprt	adenine phosphoribosyltransferase deficiency hepatocellular carcinoma
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
63840	period circadian regulator 2	Per2	advanced sleep phase syndrome 1 advanced sleep phase syndrome cocaine dependence
24212	ATPase Na+/K+ transporting subunit alpha 2	Atp1a2	alcohol use disorder alternating hemiplegia of childhood benign neonatal seizures developmental and epileptic encephalopathy 98 epilepsy familial hemiplegic migraine 2 familial hemiplegic migraine hyperhomocysteinemia hypertension migraine with aura nervous system disease
25197	ST6 beta-galactoside alpha-2,6-sialyltransferase 1	St6gal1	alcohol use disorder high grade glioma
309513	protein phosphatase 1, regulatory subunit 3C	Ppp1r3c	alcohol use disorder type 2 diabetes mellitus
192280	protein phosphatase 1, regulatory subunit 3B	Ppp1r3b	alcohol use disorder
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
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
154516	UDP glucuronosyltransferase 1 family, polypeptide A7C	Ugt1a7c	alcoholic pancreatitis cholangiocarcinoma pancreatic cancer type 2 diabetes mellitus
301595	UDP glucuronosyltransferase family 1 member A8	Ugt1a8	alcoholic pancreatitis cholangiocarcinoma pancreatic cancer
24192	aldo-keto reductase family 1 member B1	Akr1b1	allergic disease arteriosclerosis cataract diabetic neuropathy diabetic retinopathy galactosemia hepatocellular carcinoma hyperglycemia hypokalemia stomach cancer type 2 diabetes mellitus
24401	glutamic-oxaloacetic transaminase 1	Got1	amyloidosis amyotrophic lateral sclerosis cardiomyopathy pancreatic ductal adenocarcinoma transient cerebral ischemia

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