GlyCosmos Portal

Rattus norvegicus (Norway rat)

Summary

Taxonomy ID: 10116
PubChem Taxonomy: 10116

Genes (2374) Glycans (773) Glycoproteins (2549) Lectins (166) Pathways (998)

Displaying entries **701 - 725** of **2374** in total

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Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
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
116670	protein phosphatase 1, regulatory subunit 12A	Ppp1r12a
24669	protein phosphatase 1 catalytic subunit gamma	Ppp1cc	cancer congestive heart failure type 2 diabetes mellitus
25594	protein phosphatase 1 catalytic subunit beta	Ppp1cb	Noonan syndrome-like disorder with loose anagen hair 2 cancer
24668	protein phosphatase 1 catalytic subunit alpha	Ppp1ca	cancer type 2 diabetes mellitus
100360977	peptidylprolyl isomerase A (cyclophilin A)-like 4D	Ppial4d
25518	peptidylprolyl isomerase A	Ppia
117544	phosphoribosyl pyrophosphate amidotransferase	Ppat	hepatocellular carcinoma renal cell carcinoma
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
25664	peroxisome proliferator-activated receptor gamma	Pparg
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
312086	paraoxonase 3	Pon3
296851	paraoxonase 2	Pon2
84024	paraoxonase 1	Pon1
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
316091	protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-)	Pomgnt2	congenital muscular dystrophy-dystroglycanopathy type A8 muscular dystrophy-dystroglycanopathy type C8
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
310658	pogo transposable element derived with ZNF domain	Pogz
315664	protein O-glucosyltransferase 3	Poglut3
288091	protein O-glucosyltransferase 1	Poglut1	Dowling-Degos disease autosomal recessive limb-girdle muscular dystrophy type 2Z autosomal recessive limb-girdle muscular dystrophy
309686	protein O-fucosyltransferase 2	Pofut2	Down syndrome

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