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 **51 - 75** of **662** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▲
140484	protein O-fucosyltransferase 1	Pofut1	Dowling-Degos disease
80294	protein O-fucosyltransferase 2	Pofut2	Down syndrome
72136	carbohydrate sulfotransferase 14	Chst14	Ehlers-Danlos syndrome musculocontractural type 1
218271	beta-1,4-galactosyltransferase 7	B4galt7	Ehlers-Danlos syndrome spondylodysplastic type 1 Ehlers-Danlos syndrome
117592	UDP-Gal:betaGal beta 1,3-galactosyltransferase, polypeptide 6	B3galt6	Ehlers-Danlos syndrome spondylodysplastic type 2 Ehlers-Danlos syndrome spondyloepimetaphyseal dysplasia with joint laxity type 1
17939	N-acetyl galactosaminidase, alpha	Naga	Fabry disease Kanzaki disease Schindler disease type 1 angiokeratoma neuroaxonal dystrophy
246179	fukutin	Fktn	Fukuyama congenital muscular dystrophy Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M dilated cardiomyopathy 1B dilated cardiomyopathy 1X muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B4 muscular dystrophy
12091	galactosidase, beta 1	Glb1	GM1 gangliosidosis type 1 GM1 gangliosidosis type 2 GM1 gangliosidosis type 3 GM1 gangliosidosis mucopolysaccharidosis IV mucopolysaccharidosis type IVB
14667	GM2 ganglioside activator protein	Gm2a	GM2 gangliosidosis, AB variant GM2 gangliosidosis
50798	glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase	Gne	GNE myopathy sialuria
14466	glucosylceramidase beta 1	Gba1	Gaucher's disease perinatal lethal Gaucher's disease type I Gaucher's disease type II Gaucher's disease type III Gaucher's disease type IIIC Gaucher's disease Lewy body dementia Netherton syndrome Parkinson's disease Parkinsonism late onset Parkinson's disease psoriasis
18294	8-oxoguanine DNA-glycosylase 1	Ogg1	Graves' disease Parkinson's disease angiomyolipoma basal cell carcinoma breast cancer cataract cholangiocarcinoma coronary artery disease gestational diabetes head and neck squamous cell carcinoma hepatitis hypertension middle cerebral artery infarction ovarian cancer pancreatic cancer pre-eclampsia primary open angle glaucoma progressive supranuclear palsy prostate cancer pterygium renal cell carcinoma senile cataract status epilepticus transient cerebral ischemia transitional cell carcinoma type 2 diabetes mellitus
15452	hypoxanthine phosphoribosyltransferase 1	Hprt1	HRPT-related hyperuricemia Lesch-Nyhan syndrome hepatocellular carcinoma
17082	interleukin 1 receptor-like 1	Il1rl1	Hantavirus hemorrhagic fever with renal syndrome Human papillomavirus infectious disease acute myocardial infarction asthma bacterial pneumonia chronic obstructive pulmonary disease coronary artery disease hemolytic-uremic syndrome idiopathic pulmonary fibrosis paracoccidioidomycosis rhinitis tongue squamous cell carcinoma
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
22228	uncoupling protein 2 (mitochondrial, proton carrier)	Ucp2	Huntington's disease carotid artery disease congestive heart failure diabetic neuropathy end stage renal disease hypertension hypothyroidism metabolic dysfunction-associated steatotic liver disease obesity obstructive jaundice polycystic liver disease steatotic liver disease transient cerebral ischemia type 2 diabetes mellitus
67375	quinolinate phosphoribosyltransferase	Qprt	Huntington's disease
21897	toll-like receptor 1	Tlr1	IgA glomerulonephritis aspergillosis asthma collagen disease glucose metabolism disease leprosy perinatal necrotizing enterocolitis primary immunodeficiency disease pulmonary tuberculosis pyelonephritis tuberculosis
14595	UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1	B4galt1	IgA glomerulonephritis congenital disorder of glycosylation type IId congenital disorder of glycosylation endocrine system disease
15289	high mobility group box 1	Hmgb1	Kawasaki disease amyotrophic lateral sclerosis atherosclerosis brain infarction cerebral infarction colon adenocarcinoma congestive heart failure high grade glioma hydrocephalus middle cerebral artery infarction myocardial infarction obstructive jaundice periodontitis pulmonary hypertension sciatic neuropathy systemic scleroderma
14936	glycogen synthase 1, muscle	Gys1	Lafora disease cardiovascular system disease
232493	glycogen synthase 2	Gys2	Lafora disease glycogen storage disease
13853	epilepsy, progressive myoclonic epilepsy, type 2 gene alpha	Epm2a	Lafora disease progressive myoclonus epilepsy
105193	NHL repeat containing 1	Nhlrc1	Lafora disease
109880	Braf transforming gene	Braf	Langerhans-cell histiocytosis Noonan syndrome 7 Noonan syndrome with multiple lentigines 3 bile duct adenoma cancer cardiofaciocutaneous syndrome 1 cardiofaciocutaneous syndrome cardiomyopathy cholangiocarcinoma colon carcinoma colorectal adenocarcinoma colorectal cancer dysembryoplastic neuroepithelial tumor endometrial carcinoma familial melanoma germinoma high grade glioma intrahepatic cholangiocarcinoma lung cancer malignant astrocytoma melanoma pancreatic acinar cell adenocarcinoma pancreatic cancer pleomorphic xanthoastrocytoma prostate adenocarcinoma thyroid gland papillary carcinoma

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