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 **351 - 375** of **449** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
315664	protein O-glucosyltransferase 3	Poglut3
315760	poly (ADP-ribose) polymerase family, member 16	Parp16
315807	phosphatidylinositol glycan anchor biosynthesis, class B	Pigb	developmental and epileptic encephalopathy 80 sleeping sickness
316067	xylulokinase	Xylb
316091	protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-)	Pomgnt2	congenital muscular dystrophy-dystroglycanopathy type A8 muscular dystrophy-dystroglycanopathy type C8
316325	heparan sulfate 6-O-sulfotransferase 1	Hs6st1	hypogonadotropic hypogonadism 15 with or without anosmia
316533	chondroitin polymerizing factor	Chpf
316583	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7	B3gnt7
317553	interleukin 1 receptor accessory protein-like 1	Il1rapl1	intellectual disability non-syndromic X-linked intellectual disability 21
360230	serine/threonine kinase 40	Stk40
360475	ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase	Alg1	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
360604	spermatogenesis associated 20	Spata20	oligoasthenoteratozoospermia
360975	oxoglutarate dehydrogenase	Ogdh	Yoon-Bellen neurodevelopmental syndrome oxoglutarate dehydrogenase deficiency
361091	UDP-glucose glycoprotein glucosyltransferase 2	Uggt2
361142	polypeptide N-acetylgalactosaminyltransferase-like 6	Galntl6
361174	ALG11, alpha-1,2-mannosyltransferase	Alg11	congenital disorder of glycosylation Ip
361272	dehydrogenase E1 and transketolase domain containing 1	Dhtkd1	2-aminoadipic 2-oxoadipic aciduria Charcot-Marie-Tooth disease axonal type 2Q
361274	nudix hydrolase 5	Nudt5
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
361450	uronyl-2-sulfotransferase	Ust	attention deficit hyperactivity disorder
361596	isocitrate dehydrogenase (NADP(+)) 2	Idh2	D-2-hydroxyglutaric aciduria 2 acute myeloid leukemia bone remodeling disease esophagus squamous cell carcinoma hepatocellular carcinoma hepatocellular clear cell carcinoma high grade glioma intrahepatic cholangiocarcinoma lung adenocarcinoma lung cancer lung non-small cell carcinoma lung squamous cell carcinoma status epilepticus stomach cancer
361730	triokinase and FMN cyclase	Tkfc
362031	ALG14, UDP-N-acetylglucosaminyltransferase subunit	Alg14	congenital myasthenic syndrome 15
362035	N-deacetylase and N-sulfotransferase 4	Ndst4	autism spectrum disorder azoospermia intellectual disability
362093	WD repeat domain 5	Wdr5	congenital heart disease

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