GlyCosmos Portal

Rattus norvegicus (Norway rat)

Summary

Taxonomy ID: 10116
PubChem Taxonomy: 10116

Genes (449) Glycans (773) Glycoproteins (2935) Lectins (166) Pathways (1070)

Displaying entries **151 - 175** of **449** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▲
287983	ALG3, alpha-1,3- mannosyltransferase	Alg3	congenital disorder of glycosylation Id congenital disorder of glycosylation
296394	dolichyl-phosphate mannosyltransferase subunit 1, catalytic	Dpm1	congenital disorder of glycosylation Ie congenital disorder of glycosylation type I
303244	mannose-P-dolichol utilization defect 1	Mpdu1	congenital disorder of glycosylation If
315212	ALG12, alpha-1,6-mannosyltransferase	Alg12	congenital disorder of glycosylation Ig congenital disorder of glycosylation type I
293129	ALG8, alpha-1,3-glucosyltransferase	Alg8	congenital disorder of glycosylation Ih congenital disorder of glycosylation type I polycystic liver disease
313231	ALG2, alpha-1,3/1,6-mannosyltransferase	Alg2	congenital disorder of glycosylation Ii congenital myasthenic syndrome 14
300668	dolichyl-phosphate N-acetylglucosaminephosphotransferase 1	Dpagt1	congenital disorder of glycosylation Ij congenital myasthenic syndrome 13
360475	ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase	Alg1	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
367083	ALG9, alpha-1,2-mannosyltransferase	Alg9	congenital disorder of glycosylation Il congenital disorder of glycosylation type I
361174	ALG11, alpha-1,2-mannosyltransferase	Alg11	congenital disorder of glycosylation Ip
29640	dolichyl-phosphate mannosyltransferase subunit 2, regulatory	Dpm2	congenital disorder of glycosylation Iu
363160	STT3 oligosaccharyltransferase complex catalytic subunit B	Stt3b	congenital disorder of glycosylation Iw congenital disorder of glycosylation Ix
500972	STT3 oligosaccharyltransferase complex catalytic subunit A	Stt3a	congenital disorder of glycosylation Iw
295051	ALG5, dolichyl-phosphate beta-glucosyltransferase	Alg5	congenital disorder of glycosylation type I polycystic kidney disease
292090	polypeptide N-acetylgalactosaminyltransferase 2	Galnt2	congenital disorder of glycosylation type II
94273	alpha-1,6-mannosyl-glycoprotein 2-beta-N-acetylglucosaminyltransferase	Mgat2	congenital disorder of glycosylation type IIa
78947	mannosyl-oligosaccharide glucosidase	Mogs	congenital disorder of glycosylation type IIb
24390	beta-1,4-galactosyltransferase 1	B4galt1	congenital disorder of glycosylation type IId congenital disorder of glycosylation
25478	mannosidase, alpha, class 2A, member 1	Man2a1	congenital dyserythropoietic anemia systemic lupus erythematosus
362093	WD repeat domain 5	Wdr5	congenital heart disease
291212	beta-1,3-N-acetylgalactosaminyltransferase 2	B3galnt2	congenital muscular dystrophy-dystroglycanopathy type A11
306549	protein-O-mannose kinase	Pomk	congenital muscular dystrophy-dystroglycanopathy type A12 hydrocephalus muscular dystrophy-dystroglycanopathy type C12
361368	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
316091	protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-)	Pomgnt2	congenital muscular dystrophy-dystroglycanopathy type A8 muscular dystrophy-dystroglycanopathy type C8
362031	ALG14, UDP-N-acetylglucosaminyltransferase subunit	Alg14	congenital myasthenic syndrome 15

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