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 **501 - 525** of **662** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
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
18598	pyruvate dehydrogenase E1 alpha 2	Pdha2	disease of metabolism pyruvate decarboxylase deficiency retinal degeneration spermatogenic failure
18597	pyruvate dehydrogenase E1 alpha 1	Pdha1	disease of metabolism pyruvate decarboxylase deficiency retinal degeneration
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
18534	phosphoenolpyruvate carboxykinase 1, cytosolic	Pck1	Alzheimer's disease metabolic dysfunction-associated steatohepatitis type 2 diabetes mellitus
18519	K(lysine) acetyltransferase 2B	Kat2b	breast cancer esophagus squamous cell carcinoma heart disease hepatocellular carcinoma kidney disease rheumatoid arthritis
18419	otogelin	Otog	autosomal recessive nonsyndromic deafness 18B
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
18293	oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide)	Ogdh	Yoon-Bellen neurodevelopmental syndrome oxoglutarate dehydrogenase deficiency
18207	nth (endonuclease III)-like 1 (E.coli)	Nthl1	familial adenomatous polyposis 3
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
18145	NPC intracellular cholesterol transporter 1	Npc1	Niemann-Pick disease type C1 Niemann-Pick disease
18010	neuraminidase 1	Neu1	glycoproteinosis mucolipidosis
17939	N-acetyl galactosaminidase, alpha	Naga	Fabry disease Kanzaki disease Schindler disease type 1 angiokeratoma neuroaxonal dystrophy
17869	myelocytomatosis oncogene	Myc	Burkitt lymphoma acute lymphoblastic leukemia acute promyelocytic leukemia angiosarcoma breast cancer cancer chronic lymphocytic leukemia clear cell renal cell carcinoma coronary restenosis demyelinating disease hepatitis C hepatocellular carcinoma hyperparathyroidism leiomyoma liver cirrhosis lung adenocarcinoma lung cancer nephroblastoma obesity osteoporosis polycystic kidney disease 1 polycystic kidney disease prolactinoma prostate adenocarcinoma prostate cancer prostatic hypertrophy pulmonary hypertension renal cell carcinoma rhabdoid cancer thyroid gland papillary carcinoma urinary bladder cancer
17449	malate dehydrogenase 1, NAD (soluble)	Mdh1	developmental and epileptic encephalopathy 88
17448	malate dehydrogenase 2, NAD (mitochondrial)	Mdh2	brain ischemia congestive heart failure developmental and epileptic encephalopathy 51 myocardial infarction
17425	forkhead box K1	Foxk1
17423	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2	Ndst2	autism spectrum disorder azoospermia intellectual disability
17309	mannoside acetylglucosaminyltransferase 3	Mgat3
17308	mannoside acetylglucosaminyltransferase 1	Mgat1
17305	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	Mfng
17254	solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2	Slc3a2	adenoid cystic carcinoma lung adenocarcinoma lung non-small cell carcinoma lung pleomorphic carcinoma stomach carcinoma tongue squamous cell carcinoma transitional cell carcinoma
17193	methyl-CpG binding domain protein 4	Mbd4	colorectal carcinoma esophagus squamous cell carcinoma lung cancer rheumatoid arthritis uveal melanoma
17160	mannosidase 2, alpha B2	Man2b2

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