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
192281	2'-5' oligoadenylate synthetase 1A	Oas1a	primary immunodeficiency disease
171047	2'-deoxynucleoside 5'-phosphate N-hydrolase 1	Dnph1
29595	5-hydroxytryptamine receptor 2A	Htr2a	Alzheimer's disease alcohol dependence alcohol use disorder alcoholic psychosis anorexia nervosa autism spectrum disorder bladder neck obstruction chronic obstructive pulmonary disease cocaine abuse cocaine dependence congenital diaphragmatic hernia congestive heart failure depressive disorder hyperglycemia hypertension inflammatory and toxic neuropathy major depressive disorder nicotine dependence non-alcoholic fatty liver obesity obsessive-compulsive disorder pancreatitis pathological gambling schizophrenia steatotic liver disease withdrawal disorder
24638	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 1	Pfkfb1	hyperinsulinism
24640	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 2	Pfkfb2
117276	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3	Pfkfb3
54283	6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 4	Pfkfb4
81528	8-oxoguanine DNA glycosylase	Ogg1	Graves' disease Parkinson's disease angiomyolipoma basal cell carcinoma breast cancer cataract cholangiocarcinoma coronary artery disease gestational diabetes head and neck squamous cell carcinoma hepatitis hypertension middle cerebral artery infarction ovarian cancer pancreatic cancer pre-eclampsia primary open angle glaucoma progressive supranuclear palsy prostate cancer pterygium renal cell carcinoma senile cataract status epilepticus transient cerebral ischemia transitional cell carcinoma type 2 diabetes mellitus
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
25371	ADP-ribosylarginine hydrolase	Adprh
79120	ADP-ribosylation factor 4	Arf4
290880	ADP-ribosylhydrolase like 1	Adprhl1
293152	ADP-ribosyltransferase 2b	Art2b
259167	ADP-ribosyltransferase 5	Art5
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
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
362031	ALG14, UDP-N-acetylglucosaminyltransferase subunit	Alg14	congenital myasthenic syndrome 15
313231	ALG2, alpha-1,3/1,6-mannosyltransferase	Alg2	congenital disorder of glycosylation Ii congenital myasthenic syndrome 14
287983	ALG3, alpha-1,3- mannosyltransferase	Alg3	congenital disorder of glycosylation Id congenital disorder of glycosylation

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