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 **126 - 150** of **662** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▼
55981	phosphatidylinositol glycan anchor biosynthesis, class B	Pigb	developmental and epileptic encephalopathy 80 sleeping sickness
56176	phosphatidylinositol glycan anchor biosynthesis, class P	Pigp	developmental and epileptic encephalopathy 55
67574	asparagine-linked glycosylation 13	Alg13	developmental and epileptic encephalopathy 36
12952	cryptochrome circadian regulator 1	Cry1	delayed sleep phase syndrome
20532	solute carrier family 3, member 1	Slc3a1	cystinuria
192193	ER degradation enhancer, mannosidase alpha-like 1	Edem1	cystic fibrosis
100198	hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase)	H6pd	cortisone reductase deficiency 1 cortisone reductase deficiency multiple sclerosis
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
64652	nischarin	Nisch	congestive heart failure hypertension otitis media
66789	asparagine-linked glycosylation 14	Alg14	congenital myasthenic syndrome 15
215494	protein O-linked mannose beta 1,4-N-acetylglucosaminyltransferase 2	Pomgnt2	congenital muscular dystrophy-dystroglycanopathy type A8 muscular dystrophy-dystroglycanopathy type C8
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
74653	protein-O-mannose kinase	Pomk	congenital muscular dystrophy-dystroglycanopathy type A12 hydrocephalus muscular dystrophy-dystroglycanopathy type C12
97884	UDP-GalNAc:betaGlcNAc beta 1,3-galactosaminyltransferase, polypeptide 2	B3galnt2	congenital muscular dystrophy-dystroglycanopathy type A11
140858	WD repeat domain 5	Wdr5	congenital heart disease
17158	mannosidase 2, alpha 1	Man2a1	congenital dyserythropoietic anemia systemic lupus erythematosus
57377	mannosyl-oligosaccharide glucosidase	Mogs	congenital disorder of glycosylation type IIb
217664	mannoside acetylglucosaminyltransferase 2	Mgat2	congenital disorder of glycosylation type IIa
66967	ER degradation enhancer, mannosidase alpha-like 3	Edem3	congenital disorder of glycosylation type II
108148	polypeptide N-acetylgalactosaminyltransferase 2	Galnt2	congenital disorder of glycosylation type II
66248	ALG5 dolichyl-phosphate beta-glucosyltransferase	Alg5	congenital disorder of glycosylation type I polycystic kidney disease
16430	STT3, subunit of the oligosaccharyltransferase complex, homolog A (S. cerevisiae)	Stt3a	congenital disorder of glycosylation Iw
68292	STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae)	Stt3b	congenital disorder of glycosylation Iw congenital disorder of glycosylation Ix
13481	dolichyl-phosphate mannosyltransferase subunit 2, regulatory	Dpm2	congenital disorder of glycosylation Iu congenital disorder of glycosylation type I
72157	phosphoglucomutase 1	Pgm1	congenital disorder of glycosylation It endometrial cancer teratoma

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