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 **376 - 400** of **449** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
362129	glycosyltransferase-like domain containing 1	Gtdc1
362275	beta-1,4-galactosyltransferase 5	B4galt5	multiple sclerosis
362282	phosphoenolpyruvate carboxykinase 1	Pck1	Alzheimer's disease metabolic dysfunction-associated steatohepatitis type 2 diabetes mellitus
362465	transmembrane O-mannosyltransferase targeting cadherins 1	Tmtc1
362518	post-GPI attachment to proteins GalNAc transferase 4	Pgap4
362520	fukutin	Fktn	Fukuyama congenital muscular dystrophy Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2L autosomal recessive limb-girdle muscular dystrophy type 2M dilated cardiomyopathy 1B dilated cardiomyopathy 1X muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B4 muscular dystrophy
362547	ALG6, alpha-1,3-glucosyltransferase	Alg6	congenital disorder of glycosylation Ic congenital disorder of glycosylation type I
362567	protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)	Pomgnt1	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2O congenital muscular dystrophy-dystroglycanopathy type A3 lissencephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B3 muscular dystrophy retinitis pigmentosa
362760	polypeptide N-acetylgalactosaminyltransferase 16	Galnt16
362809	prostaglandin E synthase 3	Ptges3	atherosclerosis breast cancer oligodendroglioma
362924	ST3 beta-galactoside alpha-2,3-sialyltransferase 1	St3gal1
363040	ST3 beta-galactoside alpha-2,3-sialyltransferase 4	St3gal4
363160	STT3 oligosaccharyltransferase complex catalytic subunit B	Stt3b	congenital disorder of glycosylation Iw congenital disorder of glycosylation Ix
363464	phosphatidylinositol glycan anchor biosynthesis, class A	Piga	autosomal recessive congenital ichthyosis 4B multiple congenital anomalies-hypotonia-seizures syndrome 2 paroxysmal nocturnal hemoglobinuria
363618	heparan sulfate-glucosamine 3-sulfotransferase 3A1	Hs3st3a1
363799	xyloside xylosyltransferase 1	Xxylt1
364476	heparan sulfate 6-O-sulfotransferase 3	Hs6st3
364675	beta-1,4-galactosyltransferase 7	B4galt7	Ehlers-Danlos syndrome spondylodysplastic type 1 Ehlers-Danlos syndrome
364682	NHL repeat containing E3 ubiquitin protein ligase 1	Nhlrc1	Lafora disease
364901	ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5	St8sia5
365984	ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5	St6galnac5
366061	polypeptide N-acetylgalactosaminyltransferase 3	Galnt3	hyperphosphatemic familial tumoral calcinosis
366064	Beta-1,3-galactosyltransferase 1	B3galt1
366478	phosphatidylinositol glycan anchor biosynthesis, class V	Pigv	hyperphosphatasia with impaired intellectual development syndrome 1
367083	ALG9, alpha-1,2-mannosyltransferase	Alg9	congenital disorder of glycosylation Il congenital disorder of glycosylation type I

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