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 **151 - 175** of **662** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
18145	NPC intracellular cholesterol transporter 1	Npc1	Niemann-Pick disease type C1 Niemann-Pick disease
18166	neuropeptide Y receptor Y1	Npy1r	alcohol use disorder amphetamine abuse anxiety disorder childhood absence epilepsy cocaine abuse depressive disorder heroin dependence hypertension nicotine dependence obesity opiate dependence peripheral artery disease temporal lobe epilepsy visual epilepsy
18207	nth (endonuclease III)-like 1 (E.coli)	Nthl1	familial adenomatous polyposis 3
18293	oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide)	Ogdh	Yoon-Bellen neurodevelopmental syndrome oxoglutarate dehydrogenase deficiency
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
18419	otogelin	Otog	autosomal recessive nonsyndromic deafness 18B
18519	K(lysine) acetyltransferase 2B	Kat2b	breast cancer esophagus squamous cell carcinoma heart disease hepatocellular carcinoma kidney disease rheumatoid arthritis
18534	phosphoenolpyruvate carboxykinase 1, cytosolic	Pck1	Alzheimer's disease metabolic dysfunction-associated steatohepatitis type 2 diabetes mellitus
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
18597	pyruvate dehydrogenase E1 alpha 1	Pdha1	disease of metabolism pyruvate decarboxylase deficiency retinal degeneration
18598	pyruvate dehydrogenase E1 alpha 2	Pdha2	disease of metabolism pyruvate decarboxylase deficiency retinal degeneration spermatogenic failure
18605	ectonucleotide pyrophosphatase/phosphodiesterase 1	Enpp1	aortic valve disease 1 arterial calcification of infancy cardiovascular system disease end stage renal disease glioblastoma obesity ossification of the posterior longitudinal ligament of spine osteoarthritis otitis media pseudoxanthoma elasticum spondyloarthropathy tympanosclerosis type 2 diabetes mellitus
18609	pancreatic and duodenal homeobox 1	Pdx1	acute necrotizing pancreatitis cerebral infarction diabetes mellitus diabetic retinopathy hyperglycemia maturity-onset diabetes of the young type 4 maturity-onset diabetes of the young obesity pancreatic agenesis placental insufficiency type 1 diabetes mellitus type 2 diabetes mellitus
18627	period circadian clock 2	Per2	advanced sleep phase syndrome 1 advanced sleep phase syndrome cocaine dependence
18639	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 1	Pfkfb1	hyperinsulinism
18640	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2	Pfkfb2
18641	phosphofructokinase, liver, B-type	Pfkl	disease of metabolism glycogen storage disease
18642	phosphofructokinase, muscle	Pfkm	disease of metabolism glycogen storage disease VII glycogen storage disease
18648	phosphoglycerate mutase 1	Pgam1
18654	placental growth factor	Pgf	Crohn's disease amyotrophic lateral sclerosis ankylosing spondylitis asthma brain ischemia breast cancer carotid artery disease congestive heart failure diabetic neuropathy diabetic retinopathy end stage renal disease epilepsy glioblastoma hypertension limited scleroderma liver cirrhosis lymphedema myocardial infarction obesity pancreatic endocrine carcinoma pre-eclampsia pulmonary hypertension pyelonephritis renal cell carcinoma rheumatoid arthritis sickle cell anemia status epilepticus systemic lupus erythematosus temporal lobe epilepsy
18655	phosphoglycerate kinase 1	Pgk1	Parkinson's disease cancer hemolytic anemia phosphoglycerate kinase 1 deficiency
18663	phosphoglycerate kinase 2	Pgk2	Parkinson's disease cancer
18679	phosphorylase kinase alpha 1	Phka1	glycogen storage disease IXd glycogen storage disease hypothyroidism
18682	phosphorylase kinase gamma 1	Phkg1
18700	phosphatidylinositol glycan anchor biosynthesis, class A	Piga	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria

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