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 **76 - 100** of **662** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▲
72727	beta-1,3-glucuronyltransferase 3	B3gat3	Larsen-like syndrome B3GAT3 type
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
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
20597	sphingomyelin phosphodiesterase 1, acid lysosomal	Smpd1	Niemann-Pick disease type A Niemann-Pick disease type B Niemann-Pick disease Wilson disease
18145	NPC intracellular cholesterol transporter 1	Npc1	Niemann-Pick disease type C1 Niemann-Pick disease
19046	protein phosphatase 1 catalytic subunit beta	Ppp1cb	Noonan syndrome-like disorder with loose anagen hair 2 cancer
50786	heparan sulfate 6-O-sulfotransferase 2	Hs6st2	Paganini-Miozzo syndrome
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
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
18655	phosphoglycerate kinase 1	Pgk1	Parkinson's disease cancer hemolytic anemia phosphoglycerate kinase 1 deficiency
18663	phosphoglycerate kinase 2	Pgk2	Parkinson's disease cancer
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
606496	glycogen synthase kinase 3 alpha	Gsk3a	Parkinsonism amyotrophic lateral sclerosis
13807	enolase 2, gamma neuronal	Eno2	Parkinsonism brain disease breast carcinoma hypertension migraine without aura neuroendocrine carcinoma prostate cancer toxic shock syndrome urinary bladder cancer visual epilepsy
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
381694	beta-3-glucosyltransferase	B3glct	Peters plus syndrome
14380	glucose-6-phosphate dehydrogenase 2	G6pd2	Plasmodium falciparum malaria anemia cataract cerebrovascular disease cholestasis congenital hypothyroidism congenital nonspherocytic hemolytic anemia diabetes mellitus favism hemolytic anemia hepatic encephalopathy hepatocellular carcinoma hyperhomocysteinemia kidney disease malaria metabolic dysfunction-associated steatotic liver disease myocardial infarction neonatal jaundice obesity phenylketonuria renovascular hypertension transient cerebral ischemia type 1 diabetes mellitus type 2 diabetes mellitus
14381	glucose-6-phosphate dehydrogenase X-linked	G6pdx	Plasmodium falciparum malaria anemia cataract cerebrovascular disease cholestasis congenital hypothyroidism congenital nonspherocytic hemolytic anemia diabetes mellitus favism hemolytic anemia hepatic encephalopathy hepatocellular carcinoma hyperhomocysteinemia kidney disease malaria metabolic dysfunction-associated steatotic liver disease myocardial infarction neonatal jaundice obesity phenylketonuria renovascular hypertension transient cerebral ischemia type 1 diabetes mellitus type 2 diabetes mellitus
227619	mannosidase, alpha, class 1B, member 1	Man1b1	Rafiq syndrome
15212	hexosaminidase B	Hexb	Sandhoff disease lysosomal storage disease spinal muscular atrophy
110006	glucuronidase, beta	Gusb	Sly syndrome mucopolysaccharidosis peritonitis
218989	transmembrane protein 260	Tmem260	T-cell non-Hodgkin lymphoma non-Hodgkin lymphoma stomach cancer
15937	immediate early response 3	Ier3	T-cell non-Hodgkin lymphoma
15211	hexosaminidase A	Hexa	Tay-Sachs disease
59048	C1GALT1-specific chaperone 1	C1galt1c1	Tn polyagglutination syndrome hemolytic-uremic syndrome

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