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 **401 - 425** of **662** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
57377	mannosyl-oligosaccharide glucosidase	Mogs	congenital disorder of glycosylation type IIb
24070	mannose-P-dolichol utilization defect 1	Mpdu1	congenital disorder of glycosylation If
268395	N-methylpurine-DNA glycosylase	Mpg
110119	mannose phosphate isomerase	Mpi	carbohydrate metabolic disorder congenital disorder of glycosylation Ib congenital disorder of glycosylation type I
66902	methylthioadenosine phosphorylase	Mtap	biliary tract benign neoplasm common bile duct neoplasm diaphyseal medullary stenosis with malignant fibrous histiocytoma pancreatic cancer
70603	mutY DNA glycosylase	Mutyh	familial adenomatous polyposis 2 familial adenomatous polyposis stomach cancer stomach carcinoma
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
226101	myoferlin	Myof	hereditary angioedema limb-girdle muscular dystrophy
329828	myogenesis regulating glycosidase (putative)	Myorg	basal ganglia calcification
17939	N-acetyl galactosaminidase, alpha	Naga	Fabry disease Kanzaki disease Schindler disease type 1 angiokeratoma neuroaxonal dystrophy
27426	N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase	Nagpa
59027	nicotinamide phosphoribosyltransferase	Nampt	carotid artery disease coronary artery disease kidney failure metabolic dysfunction-associated steatotic liver disease middle cerebral artery infarction obesity periodontitis psoriasis pulmonary hypertension transient cerebral ischemia type 2 diabetes mellitus
94181	N-acetylneuraminic acid synthase (sialic acid synthase)	Nans	spondyloepimetaphyseal dysplasia, Genevieve-type
15531	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1	Ndst1	DiGeorge syndrome autism spectrum disorder autosomal recessive intellectual developmental disorder 46 azoospermia congenital diaphragmatic hernia intellectual disability newborn respiratory distress syndrome
17423	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2	Ndst2	autism spectrum disorder azoospermia intellectual disability
83398	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 3	Ndst3	autism spectrum disorder azoospermia intellectual disability
64580	N-deacetylase/N-sulfotransferase (heparin glucosaminyl) 4	Ndst4	autism spectrum disorder azoospermia intellectual disability
72774	nei endonuclease VIII-like 1 (E. coli)	Neil1	abdominal obesity-metabolic syndrome obesity
382913	nei like 2 (E. coli)	Neil2
234258	nei like 3 (E. coli)	Neil3	hepatocellular carcinoma
18010	neuraminidase 1	Neu1	glycoproteinosis mucolipidosis
23956	neuraminidase 2	Neu2
50877	neuraminidase 3	Neu3
241159	sialidase 4	Neu4
105193	NHL repeat containing 1	Nhlrc1	Lafora disease

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