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 **351 - 375** of **449** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
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
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
83516	PPARG coactivator 1 alpha	Ppargc1a	Alzheimer's disease Huntington's disease Parkinson's disease abdominal obesity-metabolic syndrome age related macular degeneration amblyopia amyotrophic lateral sclerosis cardiovascular system disease chronic obstructive pulmonary disease colitis congenital hypothyroidism diabetic retinopathy dilated cardiomyopathy heart disease hyperglycemia hyperthyroidism kidney cancer kidney failure macular degeneration malignant fibrous histiocytoma melanoma metabolic dysfunction-associated steatotic liver disease myocardial infarction nephrotic syndrome obesity placental insufficiency prediabetes syndrome primary biliary cholangitis renal fibrosis sciatic neuropathy steatotic liver disease type 2 diabetes mellitus
117544	phosphoribosyl pyrophosphate amidotransferase	Ppat	hepatocellular carcinoma renal cell carcinoma
24668	protein phosphatase 1 catalytic subunit alpha	Ppp1ca	cancer type 2 diabetes mellitus
25594	protein phosphatase 1 catalytic subunit beta	Ppp1cb	Noonan syndrome-like disorder with loose anagen hair 2 cancer
24669	protein phosphatase 1 catalytic subunit gamma	Ppp1cc	cancer congestive heart failure type 2 diabetes mellitus
58977	protein phosphatase 1, regulatory (inhibitor) subunit 1A	Ppp1r1a
192361	protein phosphatase 1, regulatory (inhibitor) subunit 2	Ppp1r2
192280	protein phosphatase 1, regulatory subunit 3B	Ppp1r3b	alcohol use disorder
309513	protein phosphatase 1, regulatory subunit 3C	Ppp1r3c	alcohol use disorder 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
362809	prostaglandin E synthase 3	Ptges3	atherosclerosis breast cancer oligodendroglioma
25739	glycogen phosphorylase B	Pygb
64035	glycogen phosphorylase L	Pygl	glycogen storage disease VI glycogen storage disease lactic acidosis
293504	quinolinate phosphoribosyltransferase	Qprt	Huntington's disease
64016	queuine tRNA-ribosyltransferase catalytic subunit 1	Qtrt1
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
81759	renin binding protein	Renbp
60433	RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	Rfng
25106	regucalcin	Rgn	familial hyperlipidemia hepatocellular carcinoma stomach cancer
299841	ribitol xylosyltransferase 1	Rxylt1	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A10
287545	sterile alpha and TIR motif containing 1	Sarm1	amyotrophic lateral sclerosis neurodegenerative disease
25044	serine dehydratase	Sds
308586	secretory blood group 1	Sec1	vitamin B12 deficiency

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