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 **376 - 400** of **449** in total

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Gene ID	Gene Name ▲	Gene Symbol	Disease Ontology
293181	polypeptide N-acetylgalactosaminyltransferase 18	Galnt18
292090	polypeptide N-acetylgalactosaminyltransferase 2	Galnt2	congenital disorder of glycosylation type II
366061	polypeptide N-acetylgalactosaminyltransferase 3	Galnt3	hyperphosphatemic familial tumoral calcinosis
500826	polypeptide N-acetylgalactosaminyltransferase 4	Galnt4
83627	polypeptide N-acetylgalactosaminyltransferase 5	Galnt5
100361647	polypeptide N-acetylgalactosaminyltransferase 6	Galnt6
29750	polypeptide N-acetylgalactosaminyltransferase 7	Galnt7
499968	polypeptide N-acetylgalactosaminyltransferase-like 5	Galntl5
361142	polypeptide N-acetylgalactosaminyltransferase-like 6	Galntl6
362518	post-GPI attachment to proteins GalNAc transferase 4	Pgap4
83535	potassium inwardly-rectifying channel, subfamily J, member 11	Kcnj11	Parkinsonism diabetes mellitus familial hyperinsulinemic hypoglycemia 2 hyperinsulinism hypertension maturity-onset diabetes of the young type 13 permanent neonatal diabetes mellitus prediabetes syndrome sciatic neuropathy status epilepticus type 2 diabetes mellitus visual epilepsy
84020	potassium voltage-gated channel subfamily Q member 1	Kcnq1	Jervell-Lange Nielsen syndrome atrial fibrillation familial atrial fibrillation hypertension long QT syndrome 1 long QT syndrome seminoma short QT syndrome type 2 diabetes mellitus
288583	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	Plod3	hepatocellular carcinoma hypothyroidism
25737	proliferating cell nuclear antigen	Pcna	Lewy body dementia ataxia-telangiectasia-like disorder-2 brain ischemia hepatocellular carcinoma hypothyroidism invasive ductal carcinoma leiomyoma liver cancer mucositis nephroblastoma obstructive jaundice osteoporosis renal cell carcinoma sciatic neuropathy seminoma stomach cancer transient cerebral ischemia
362809	prostaglandin E synthase 3	Ptges3	atherosclerosis breast cancer oligodendroglioma
311551	protein O-fucosyltransferase 1	Pofut1	Dowling-Degos disease
309686	protein O-fucosyltransferase 2	Pofut2	Down syndrome
288091	protein O-glucosyltransferase 1	Poglut1	Dowling-Degos disease autosomal recessive limb-girdle muscular dystrophy type 2Z autosomal recessive limb-girdle muscular dystrophy
315664	protein O-glucosyltransferase 3	Poglut3
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
316091	protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-)	Pomgnt2	congenital muscular dystrophy-dystroglycanopathy type A8 muscular dystrophy-dystroglycanopathy type C8
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
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

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