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 **276 - 300** of **662** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▼
606496	glycogen synthase kinase 3 alpha	Gsk3a	Parkinsonism amyotrophic lateral sclerosis
12846	catechol-O-methyltransferase	Comt	Parkinsonism alcohol dependence alcohol use disorder amphetamine abuse attention deficit hyperactivity disorder autism spectrum disorder bipolar disorder breast cancer bulimia nervosa cannabis abuse cannabis dependence cocaine dependence cognitive disorder drug dependence endometrial cancer eumycotic mycetoma fibromyalgia heroin dependence hypertension intermittent explosive disorder leiomyoma lung cancer morphine dependence neonatal abstinence syndrome nicotine dependence obesity obsessive-compulsive disorder opiate dependence ovarian cancer pathological gambling polycystic ovary syndrome pre-eclampsia prostate cancer psoriasis renal cell carcinoma schizophrenia uremia urinary bladder cancer vitiligo withdrawal disorder
18663	phosphoglycerate kinase 2	Pgk2	Parkinson's disease cancer
18655	phosphoglycerate kinase 1	Pgk1	Parkinson's disease cancer hemolytic anemia phosphoglycerate kinase 1 deficiency
11652	thymoma viral proto-oncogene 2	Akt2	Parkinson's disease alcohol use disorder cancer colorectal cancer endometrial cancer hepatocellular carcinoma high grade glioma hypertension hypoglycemia hypoinsulinemic hypoglycemia with hemihypertrophy ischemia malignant astrocytoma obesity ovarian carcinoma polycystic ovary syndrome prostate adenocarcinoma prostate cancer prostate carcinoma type 2 diabetes mellitus
14751	glucose-6-phosphate isomerase 1	Gpi1	Parkinson's disease acute lymphoblastic leukemia acute myeloid leukemia congenital hemolytic anemia congenital nonspherocytic hemolytic anemia heart disease intellectual disability neuromuscular disease
50786	heparan sulfate 6-O-sulfotransferase 2	Hs6st2	Paganini-Miozzo syndrome
19046	protein phosphatase 1 catalytic subunit beta	Ppp1cb	Noonan syndrome-like disorder with loose anagen hair 2 cancer
18145	NPC intracellular cholesterol transporter 1	Npc1	Niemann-Pick disease type C1 Niemann-Pick disease
20597	sphingomyelin phosphodiesterase 1, acid lysosomal	Smpd1	Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease Wilson disease
26903	dysferlin	Dysf	Miyoshi muscular dystrophy 1 autosomal recessive limb-girdle muscular dystrophy type 2B distal myopathy with anterior tibial onset distal myopathy limb-girdle muscular dystrophy muscular dystrophy
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
72727	beta-1,3-glucuronyltransferase 3	B3gat3	Larsen-like syndrome B3GAT3 type
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
105193	NHL repeat containing 1	Nhlrc1	Lafora disease
13853	epilepsy, progressive myoclonic epilepsy, type 2 gene alpha	Epm2a	Lafora disease progressive myoclonus epilepsy
232493	glycogen synthase 2	Gys2	Lafora disease glycogen storage disease
14936	glycogen synthase 1, muscle	Gys1	Lafora disease cardiovascular 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
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
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
67375	quinolinate phosphoribosyltransferase	Qprt	Huntington's disease
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
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
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

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