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 **226 - 250** of **662** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▲
74653	protein-O-mannose kinase	Pomk	congenital muscular dystrophy-dystroglycanopathy type A12 hydrocephalus muscular dystrophy-dystroglycanopathy type C12
16795	LARGE xylosyl- and glucuronyltransferase 1	Large1	congenital muscular dystrophy-dystroglycanopathy type A6 facioscapulohumeral muscular dystrophy muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B6
215494	protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2	Pomgnt2	congenital muscular dystrophy-dystroglycanopathy type A8 muscular dystrophy-dystroglycanopathy type C8
66789	asparagine-linked glycosylation 14	Alg14	congenital myasthenic syndrome 15
64652	nischarin	Nisch	congestive heart failure hypertension otitis media
103988	glucokinase	Gck	coronary artery disease diabetes mellitus familial hyperinsulinemic hypoglycemia 3 gestational diabetes glucose metabolism disease hyperglycemia hyperinsulinemic hypoglycemia hyperinsulinism hypertension hypoglycemia maturity-onset diabetes of the young type 2 maturity-onset diabetes of the young obesity permanent neonatal diabetes mellitus steatotic liver disease type 2 diabetes mellitus
100198	hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase)	H6pd	cortisone reductase deficiency 1 cortisone reductase deficiency multiple sclerosis
192193	ER degradation enhancer, mannosidase alpha-like 1	Edem1	cystic fibrosis
20532	solute carrier family 3, member 1	Slc3a1	cystinuria
12952	cryptochrome circadian regulator 1	Cry1	delayed sleep phase syndrome
67574	asparagine-linked glycosylation 13	Alg13	developmental and epileptic encephalopathy 36
56176	phosphatidylinositol glycan anchor biosynthesis, class P	Pigp	developmental and epileptic encephalopathy 55
55981	phosphatidylinositol glycan anchor biosynthesis, class B	Pigb	developmental and epileptic encephalopathy 80 sleeping sickness
17449	malate dehydrogenase 1, NAD (soluble)	Mdh1	developmental and epileptic encephalopathy 88
15117	hyaluronan synthase 2	Has2	diabetes insipidus middle cerebral artery infarction pulmonary hypertension
71665	fucosidase, alpha-L- 1, tissue	Fuca1	diabetes mellitus diabetic retinopathy fucosidosis type 1 diabetes mellitus type 2 diabetes mellitus
18642	phosphofructokinase, muscle	Pfkm	disease of metabolism glycogen storage disease VII glycogen storage disease
56421	phosphofructokinase, platelet	Pfkp	disease of metabolism glycogen storage disease
18641	phosphofructokinase, liver, B-type	Pfkl	disease of metabolism glycogen storage disease
16828	lactate dehydrogenase A	Ldha	disease of metabolism hyperglycemia hypertension
18746	pyruvate kinase, muscle	Pkm	disease of metabolism hypertension
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
22256	uracil DNA glycosylase	Ung	dysgammaglobulinemia immunodeficiency with hyper IgM type 5
74155	ERBB receptor feedback inhibitor 1	Errfi1	endometrial cancer osteoarthritis

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