GlyCosmos Portal

Mus musculus (house mouse)

Summary

Taxonomy ID: 10090
PubChem Taxonomy: 10090

Genes (662) Glycans (1270) Glycoproteins (13000) Lectins (276) Pathways (1335)

Displaying entries **101 - 125** of **662** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
105787	protein kinase, AMP-activated, alpha 1 catalytic subunit	Prkaa1	Huntington's disease Parkinson's disease breast cancer cholestasis colon cancer lung non-small cell carcinoma obesity type 2 diabetes mellitus
212974	protein glucosylgalactosylhydroxylysine glucosidase	Pgghg
215494	protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2	Pomgnt2	congenital muscular dystrophy-dystroglycanopathy type A8 muscular dystrophy-dystroglycanopathy type C8
68273	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	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
68304	protein O-glucosyltransferase 3	Poglut3
72050	protein O-glucosyltransferase 2	Poglut2
224143	protein O-glucosyltransferase 1	Poglut1	Dowling-Degos disease autosomal recessive limb-girdle muscular dystrophy type 2Z autosomal recessive limb-girdle muscular dystrophy
80294	protein O-fucosyltransferase 2	Pofut2	Down syndrome
140484	protein O-fucosyltransferase 1	Pofut1	Dowling-Degos disease
56351	prostaglandin E synthase 3	Ptges3	atherosclerosis breast cancer oligodendroglioma
18538	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
26433	procollagen-lysine, 2-oxoglutarate 5-dioxygenase 3	Plod3	hepatocellular carcinoma hypothyroidism
16535	potassium voltage-gated channel, subfamily Q, member 1	Kcnq1	Beckwith-Wiedemann syndrome Jervell-Lange Nielsen syndrome atrial fibrillation familial atrial fibrillation heart conduction disease hypertension long QT syndrome 1 long QT syndrome seminoma short QT syndrome type 2 diabetes mellitus
16514	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
67063	post-GPI attachment to proteins GalNAc transferase 4	Pgap4
108150	polypeptide N-acetylgalactosaminyltransferase 7	Galnt7
207839	polypeptide N-acetylgalactosaminyltransferase 6	Galnt6
241391	polypeptide N-acetylgalactosaminyltransferase 5	Galnt5
14426	polypeptide N-acetylgalactosaminyltransferase 4	Galnt4
14425	polypeptide N-acetylgalactosaminyltransferase 3	Galnt3	hyperphosphatemic familial tumoral calcinosis
108148	polypeptide N-acetylgalactosaminyltransferase 2	Galnt2	congenital disorder of glycosylation type II
233733	polypeptide N-acetylgalactosaminyltransferase 18	Galnt18
212996	polypeptide N-acetylgalactosaminyltransferase 17	Galnt17
108760	polypeptide N-acetylgalactosaminyltransferase 16	Galnt16
78754	polypeptide N-acetylgalactosaminyltransferase 15	Galnt15

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