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 **251 - 275** of **449** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
292325	UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 6	B3gnt6
292485	alpha-L-fucosidase 2	Fuca2
292804	glucose-6-phosphate isomerase	Gpi	Parkinson's disease acute lymphoblastic leukemia acute myeloid leukemia congenital hemolytic anemia congenital nonspherocytic hemolytic anemia heart disease intellectual disability neuromuscular disease
292999	chondroitin sulfate synthase 1	Chsy1	temtamy preaxial brachydactyly syndrome
293129	ALG8, alpha-1,3-glucosyltransferase	Alg8	congenital disorder of glycosylation Ih congenital disorder of glycosylation type I polycystic liver disease
293152	ADP-ribosyltransferase 2b	Art2b
293181	polypeptide N-acetylgalactosaminyltransferase 18	Galnt18
293451	heparan sulfate-glucosamine 3-sulfotransferase 2	Hs3st2	colon cancer lung cancer lung non-small cell carcinoma pancreatic cancer
293504	quinolinate phosphoribosyltransferase	Qprt	Huntington's disease
293628	chitinase domain containing 1	Chid1
293667	beta-1,4-glucuronyltransferase 1	B4gat1	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A13 muscular dystrophy-dystroglycanopathy type B1
293722	beta-1,3-glucuronyltransferase 3	B3gat3	Larsen-like syndrome B3GAT3 type
294449	heparan sulfate-glucosamine 3-sulfotransferase 5	Hs3st5
294673	hexosaminidase subunit beta	Hexb	Sandhoff disease lysosomal storage disease spinal muscular atrophy
295051	ALG5, dolichyl-phosphate beta-glucosyltransferase	Alg5	congenital disorder of glycosylation type I polycystic kidney disease
295430	N-deacetylase and N-sulfotransferase 3	Ndst3	autism spectrum disorder azoospermia intellectual disability
295934	carbohydrate sulfotransferase 1	Chst1
296117	galactokinase 2	Galk2
296394	dolichyl-phosphate mannosyltransferase subunit 1, catalytic	Dpm1	congenital disorder of glycosylation Ie congenital disorder of glycosylation type I
296504	histo-blood group ABO system transferase 2	Abo2	COVID-19 Plasmodium falciparum malaria acute lymphoblastic leukemia asthma echinococcosis gallbladder carcinoma graft-versus-host disease hemolytic anemia hepatitis hypertension leukemia pancreatic cancer pneumonia pulmonary sarcoidosis severe acute respiratory syndrome
296564	fucosyltransferase 7	Fut7	candidiasis
296577	glycosyltransferase 6 domain containing 1	Glt6d1
296733	chondroitin polymerizing factor 2	Chpf2
297508	nicotinamide phosphoribosyltransferase	Nampt	carotid artery disease coronary artery disease kidney failure metabolic dysfunction-associated steatotic liver disease middle cerebral artery infarction obesity periodontitis psoriasis pulmonary hypertension transient cerebral ischemia type 2 diabetes mellitus
297554	chondroitin sulfate N-acetylgalactosaminyltransferase 2	Csgalnact2

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