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 **1 - 25** of **449** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
171553	alpha 1,3-galactosyltransferase 2	A3galt2
63888	alpha 1,4-galactosyltransferase	A4galt
685758	alpha-1,4-N-acetylglucosaminyltransferase	A4gnt	pancreatic cancer
303953	abhydrolase domain containing 10, depalmitoylase	Abhd10
100301568	ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase	Abo	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
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
65270	histo-blood group ABO system transferase 3	Abo3	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
24158	acyl-CoA dehydrogenase medium chain	Acadm	medium chain acyl-CoA dehydrogenase deficiency metabolic dysfunction-associated steatotic liver disease
59320	adenylate cyclase 10	Adcy10
25371	ADP-ribosylarginine hydrolase	Adprh
290880	ADP-ribosylhydrolase like 1	Adprhl1
24925	adrenoceptor beta 1	Adrb1	aortic valve stenosis chronic obstructive pulmonary disease congestive heart failure cystic fibrosis dilated cardiomyopathy hyperglycemia hypertension low tension glaucoma myocardial infarction nephrosclerosis obstructive sleep apnea periodontitis renovascular hypertension type 1 diabetes mellitus
78959	aldo-keto reductase family 1 member A1	Akr1a1	breast cancer lung adenocarcinoma
24192	aldo-keto reductase family 1 member B1	Akr1b1	allergic disease arteriosclerosis cataract diabetic neuropathy diabetic retinopathy galactosemia hepatocellular carcinoma hyperglycemia hypokalemia stomach cancer type 2 diabetes mellitus
24185	AKT serine/threonine kinase 1	Akt1	Cowden syndrome 6 Parkinson's disease Proteus syndrome alcohol use disorder autosomal recessive polycystic kidney disease bipolar disorder brain ischemia breast cancer cancer chronic myeloid leukemia colon cancer colorectal cancer diabetic retinopathy esophageal cancer esophagus squamous cell carcinoma hepatocellular carcinoma hypertension idiopathic pulmonary fibrosis impotence in situ carcinoma intermediate coronary syndrome invasive ductal carcinoma lung non-small cell carcinoma malignant astrocytoma myocardial infarction ovarian cancer pancreatic cancer pancreatic intraductal papillary-mucinous neoplasm paraplegia prostate adenocarcinoma prostate cancer pulmonary tuberculosis renal cell carcinoma schizophrenia type 2 diabetes mellitus ureteral obstruction urinary bladder cancer vulva cancer
25233	AKT serine/threonine kinase 2	Akt2	Parkinson's disease alcohol use disorder cancer colorectal cancer endometrial cancer hepatocellular carcinoma high grade glioma hypertension hypoglycemia hypoinsulinemic hypoglycemia with hemihypertrophy ischemia malignant astrocytoma obesity ovarian carcinoma polycystic ovary syndrome prostate adenocarcinoma prostate cancer prostate carcinoma type 2 diabetes mellitus
24188	aldehyde dehydrogenase 1 family, member A1	Aldh1a1	pancreatic cancer
24189	aldolase, fructose-bisphosphate A	Aldoa
24191	aldolase, fructose-bisphosphate C	Aldoc	autoimmune disease of the nervous system borna disease hepatocellular carcinoma
360475	ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase	Alg1	congenital disorder of glycosylation Ik congenital disorder of glycosylation type I congenital disorder of glycosylation
245960	ALG10, alpha-1,2-glucosyltransferase	Alg10	long QT syndrome 2 nonsyndromic deafness
361174	ALG11, alpha-1,2-mannosyltransferase	Alg11	congenital disorder of glycosylation Ip
315212	ALG12, alpha-1,6-mannosyltransferase	Alg12	congenital disorder of glycosylation Ig congenital disorder of glycosylation type I
108349244	ALG13, UDP-N-acetylglucosaminyltransferase subunit	Alg13
300284	ALG13, UDP-N-acetylglucosaminyltransferase subunit like 1	Alg13l1	developmental and epileptic encephalopathy 36

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