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 **101 - 125** of **449** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▼
292090	polypeptide N-acetylgalactosaminyltransferase 2	Galnt2	congenital disorder of glycosylation type II
295051	ALG5, dolichyl-phosphate beta-glucosyltransferase	Alg5	congenital disorder of glycosylation type I polycystic kidney disease
500972	STT3 oligosaccharyltransferase complex catalytic subunit A	Stt3a	congenital disorder of glycosylation Iw
363160	STT3 oligosaccharyltransferase complex catalytic subunit B	Stt3b	congenital disorder of glycosylation Iw congenital disorder of glycosylation Ix
29640	dolichyl-phosphate mannosyltransferase subunit 2, regulatory	Dpm2	congenital disorder of glycosylation Iu
361174	ALG11, alpha-1,2-mannosyltransferase	Alg11	congenital disorder of glycosylation Ip
367083	ALG9, alpha-1,2-mannosyltransferase	Alg9	congenital disorder of glycosylation Il congenital disorder of glycosylation type I
360475	ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase	Alg1	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
300668	dolichyl-phosphate N-acetylglucosaminephosphotransferase 1	Dpagt1	congenital disorder of glycosylation Ij congenital myasthenic syndrome 13
313231	ALG2, alpha-1,3/1,6-mannosyltransferase	Alg2	congenital disorder of glycosylation Ii congenital myasthenic syndrome 14
293129	ALG8, alpha-1,3-glucosyltransferase	Alg8	congenital disorder of glycosylation Ih congenital disorder of glycosylation type I polycystic liver disease
315212	ALG12, alpha-1,6-mannosyltransferase	Alg12	congenital disorder of glycosylation Ig congenital disorder of glycosylation type I
303244	mannose-P-dolichol utilization defect 1	Mpdu1	congenital disorder of glycosylation If
296394	dolichyl-phosphate mannosyltransferase subunit 1, catalytic	Dpm1	congenital disorder of glycosylation Ie congenital disorder of glycosylation type I
287983	ALG3, alpha-1,3- mannosyltransferase	Alg3	congenital disorder of glycosylation Id congenital disorder of glycosylation
362547	ALG6, alpha-1,3-glucosyltransferase	Alg6	congenital disorder of glycosylation Ic congenital disorder of glycosylation type I
313233	polypeptide N-acetylgalactosaminyltransferase 12	Galnt12	colorectal cancer
293451	heparan sulfate-glucosamine 3-sulfotransferase 2	Hs3st2	colon cancer lung cancer lung non-small cell carcinoma pancreatic cancer
498332	coenzyme Q2, polyprenyltransferase	Coq2	coenzyme Q10 deficiency disease glucose intolerance multiple system atrophy nephrotic syndrome primary coenzyme Q10 deficiency 1
298003	galactose-1-phosphate uridylyltransferase	Galt	classic galactosemia galactosemia
252900	diacylglycerol O-acyltransferase 2	Dgat2	chronic kidney disease metabolic dysfunction-associated steatotic liver disease premature menopause steatotic liver disease
83504	Klotho	Kl	chronic kidney disease coronary artery disease end stage renal disease familial hyperlipidemia hyperphosphatemic familial tumoral calcinosis hypertension intracranial embolism kidney disease kidney failure pulmonary emphysema retinitis pigmentosa secondary hyperparathyroidism spondylosis type 2 diabetes mellitus
396552	UDP glucuronosyltransferase family 1 member A9	Ugt1a9	cholangiocarcinoma
315219	thymidine phosphorylase	Tymp	cervical squamous cell carcinoma common bile duct neoplasm ductal carcinoma in situ endometrial cancer gallbladder carcinoma lung non-small cell carcinoma mitochondrial DNA depletion syndrome 1 mitochondrial encephalomyopathy ovarian cancer pancreatic cancer pancreatic ductal carcinoma renal cell carcinoma seminoma teratoma transitional cell carcinoma urinary bladder cancer
25283	glutamate-cysteine ligase, catalytic subunit	Gclc	cataract colorectal cancer cystic fibrosis glutamate-cysteine ligase deficiency hemolytic anemia liver cirrhosis myocardial infarction pulmonary emphysema

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