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 **26 - 50** of **449** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
64201	solute carrier family 25 member 11	Slc25a11	paraganglioma
50622	solute carrier family 23 member 2	Slc23a2
315344	single-strand-selective monofunctional uracil-DNA glycosylase 1	Smug1
360230	serine/threonine kinase 40	Stk40
25044	serine dehydratase	Sds
308586	secretory blood group 1	Sec1	vitamin B12 deficiency
299841	ribitol xylosyltransferase 1	Rxylt1	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A10
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
25106	regucalcin	Rgn	familial hyperlipidemia hepatocellular carcinoma stomach cancer
293504	quinolinate phosphoribosyltransferase	Qprt	Huntington's disease
64016	queuine tRNA-ribosyltransferase catalytic subunit 1	Qtrt1
25630	pyruvate kinase M1/2	Pkm	disease of metabolism hypertension
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
289950	pyruvate dehydrogenase E1 subunit beta	Pdhb	pyruvate decarboxylase deficiency
117098	pyruvate dehydrogenase E1 subunit alpha 2	Pdha2	disease of metabolism pyruvate decarboxylase deficiency retinal degeneration spermatogenic failure
25104	pyruvate carboxylase	Pc	pyruvate carboxylase deficiency disease
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
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
306549	protein-O-mannose kinase	Pomk	congenital muscular dystrophy-dystroglycanopathy type A12 hydrocephalus muscular dystrophy-dystroglycanopathy type C12
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
192361	protein phosphatase 1, regulatory (inhibitor) subunit 2	Ppp1r2
58977	protein phosphatase 1, regulatory (inhibitor) subunit 1A	Ppp1r1a
24669	protein phosphatase 1 catalytic subunit gamma	Ppp1cc	cancer congestive heart failure type 2 diabetes mellitus

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