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 ▲
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
14042	exostosin glycosyltransferase 1	Ext1	autism spectrum disorder chondrosarcoma hereditary multiple exostoses
94192	core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase, 1	C1galt1	autoimmune disease of blood
11676	aldolase C, fructose-bisphosphate	Aldoc	autoimmune disease of the nervous system borna disease hepatocellular carcinoma
22619	sialic acid acetylesterase	Siae	autoimmune disease
18700	phosphatidylinositol glycan anchor biosynthesis, class A	Piga	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
20322	sorbitol dehydrogenase	Sord	autosomal recessive distal hereditary motor neuronopathy 8 cataract diabetic neuropathy obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy
20441	ST3 beta-galactoside alpha-2,3-sialyltransferase 3	St3gal3	autosomal recessive intellectual developmental disorder 12 developmental and epileptic encephalopathy 15
18419	otogelin	Otog	autosomal recessive nonsyndromic deafness 18B
628870	otogelin-like	Otogl	autosomal recessive nonsyndromic deafness 84B
70551	transmembrane and tetratricopeptide repeat containing 4	Tmtc4	autosomal recessive nonsyndromic deafness
329828	myogenesis regulating glycosidase (putative)	Myorg	basal ganglia calcification
110173	mannosidase, beta A, lysosomal	Manba	beta-mannosidosis
66902	methylthioadenosine phosphorylase	Mtap	biliary tract benign neoplasm common bile duct neoplasm diaphyseal medullary stenosis with malignant fibrous histiocytoma pancreatic cancer
12974	citrate synthase	Cs	bipolar disorder congestive heart failure dilated cardiomyopathy hyperthyroidism hypertrophic cardiomyopathy hypothyroidism limb ischemia myocardial infarction retinal degeneration
11911	activating transcription factor 4	Atf4	borna disease prostate carcinoma pulmonary venoocclusive disease
17448	malate dehydrogenase 2, NAD (mitochondrial)	Mdh2	brain ischemia congestive heart failure developmental and epileptic encephalopathy 51 myocardial infarction
234407	collagen beta(1-O)galactosyltransferase 1	Colgalt1	brain small vessel disease 3
21416	transcription factor 7 like 2, T cell specific, HMG box	Tcf7l2	breast cancer colorectal cancer diabetes mellitus gestational diabetes obesity pancreatic cancer prostate cancer type 2 diabetes mellitus
18519	K(lysine) acetyltransferase 2B	Kat2b	breast cancer esophagus squamous cell carcinoma heart disease hepatocellular carcinoma kidney disease rheumatoid arthritis
58810	aldo-keto reductase family 1, member A1	Akr1a1	breast cancer lung adenocarcinoma
21991	triosephosphate isomerase 1	Tpi1	cancer carbohydrate metabolic disorder neurodegenerative disease ocular hypertension triosephosphate isomerase deficiency
109785	phosphoglucomutase 3	Pgm3	cancer cervical cancer immunodeficiency 23 teratoma

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