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 **201 - 225** of **662** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▲
54128	phosphomannomutase 2	Pmm2	congenital disorder of glycosylation Ia congenital disorder of glycosylation type I congenital disorder of glycosylation
29858	phosphomannomutase 1	Pmm1	congenital disorder of glycosylation Ia congenital disorder of glycosylation type I
320438	ALG6 alpha-1,3-glucosyltransferase	Alg6	congenital disorder of glycosylation Ic congenital disorder of glycosylation type I
208624	ALG3 alpha-1,3- mannosyltransferase	Alg3	congenital disorder of glycosylation Id congenital disorder of glycosylation
13480	dolichyl-phosphate mannosyltransferase subunit 1, catalytic	Dpm1	congenital disorder of glycosylation Ie congenital disorder of glycosylation type I
24070	mannose-P-dolichol utilization defect 1	Mpdu1	congenital disorder of glycosylation If
223774	ALG12 alpha-1,6-mannosyltransferase	Alg12	congenital disorder of glycosylation Ig congenital disorder of glycosylation type I
381903	ALG8 alpha-1,3-glucosyltransferase	Alg8	congenital disorder of glycosylation Ih congenital disorder of glycosylation type I polycystic liver disease
56737	ALG2 alpha-1,3/1,6-mannosyltransferase	Alg2	congenital disorder of glycosylation Ii congenital myasthenic syndrome 14
13478	dolichyl-phosphate N-acetylglucosaminephosphotransferase 1	Dpagt1	congenital disorder of glycosylation Ij congenital myasthenic syndrome 13
208211	ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase	Alg1	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
102580	ALG9 alpha-1,2-mannosyltransferase	Alg9	congenital disorder of glycosylation Il congenital disorder of glycosylation type I
207958	ALG11 alpha-1,2-mannosyltransferase	Alg11	congenital disorder of glycosylation Ip
72157	phosphoglucomutase 1	Pgm1	congenital disorder of glycosylation It endometrial cancer teratoma
13481	dolichyl-phosphate mannosyltransferase subunit 2, regulatory	Dpm2	congenital disorder of glycosylation Iu congenital disorder of glycosylation type I
68292	STT3, subunit of the oligosaccharyltransferase complex, homolog B (S. cerevisiae)	Stt3b	congenital disorder of glycosylation Iw congenital disorder of glycosylation Ix
16430	STT3, subunit of the oligosaccharyltransferase complex, homolog A (S. cerevisiae)	Stt3a	congenital disorder of glycosylation Iw
66248	ALG5 dolichyl-phosphate beta-glucosyltransferase	Alg5	congenital disorder of glycosylation type I polycystic kidney disease
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
217664	mannoside acetylglucosaminyltransferase 2	Mgat2	congenital disorder of glycosylation type IIa
57377	mannosyl-oligosaccharide glucosidase	Mogs	congenital disorder of glycosylation type IIb
17158	mannosidase 2, alpha 1	Man2a1	congenital dyserythropoietic anemia systemic lupus erythematosus
140858	WD repeat domain 5	Wdr5	congenital heart disease
97884	UDP-GalNAc:betaGlcNAc beta 1,3-galactosaminyltransferase, polypeptide 2	B3galnt2	congenital muscular dystrophy-dystroglycanopathy type A11

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