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
171106	interleukin 1 receptor-like 2	Il1rl2
65038	inositol polyphosphate phosphatase-like 1	Inppl1	hypertension obesity type 2 diabetes mellitus
24505	insulin 1	Ins1	Alzheimer's disease cholangiocarcinoma diabetes mellitus diabetic retinopathy disease of metabolism gestational diabetes hyperinsulinism hyperuricemia insulinoma maturity-onset diabetes of the young type 10 osteoarthritis pancreatic cancer pancreatic ductal carcinoma permanent neonatal diabetes mellitus prostate cancer sleep disorder steatotic liver disease type 1 diabetes mellitus 2 type 1 diabetes mellitus type 2 diabetes mellitus
24506	insulin 2	Ins2	Alzheimer's disease cholangiocarcinoma diabetes mellitus diabetic retinopathy disease of metabolism gestational diabetes hyperinsulinism hypertension hyperuricemia insulinoma maturity-onset diabetes of the young type 10 maturity-onset diabetes of the young neonatal diabetes osteoarthritis pancreatic cancer pancreatic ductal carcinoma permanent neonatal diabetes mellitus prostate cancer steatotic liver disease type 1 diabetes mellitus 2 type 1 diabetes mellitus type 2 diabetes mellitus
83535	potassium inwardly-rectifying channel, subfamily J, member 11	Kcnj11	Parkinsonism diabetes mellitus familial hyperinsulinemic hypoglycemia 2 hyperinsulinism hypertension maturity-onset diabetes of the young type 13 permanent neonatal diabetes mellitus prediabetes syndrome sciatic neuropathy status epilepticus type 2 diabetes mellitus visual epilepsy
84020	potassium voltage-gated channel subfamily Q member 1	Kcnq1	Jervell-Lange Nielsen syndrome atrial fibrillation familial atrial fibrillation hypertension long QT syndrome 1 long QT syndrome seminoma short QT syndrome type 2 diabetes mellitus
25659	ketohexokinase	Khk	essential fructosuria
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
24528	lactalbumin, alpha	Lalba	gastroenteritis
114515	LanC like glutathione S-transferase 1	Lancl1
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
311202	LARGE xylosyl- and glucuronyltransferase 2	Large2
24533	lactate dehydrogenase A	Ldha	disease of metabolism hyperglycemia hypertension
25608	leptin	Lep	Alzheimer's disease Huntington's disease Parkinson's disease abdominal obesity-metabolic syndrome 1 abdominal obesity-metabolic syndrome acute pancreatitis adult respiratory distress syndrome alcohol dependence alcoholic liver cirrhosis asthma breast cancer chronic obstructive pulmonary disease congenital leptin deficiency cystic fibrosis end stage renal disease familial hyperlipidemia gestational diabetes glucose intolerance hepatocellular carcinoma hepatocellular clear cell carcinoma hyperinsulinism hypertension hypogonadism lipid metabolism disorder lung non-small cell carcinoma metabolic dysfunction-associated steatotic liver disease obesity obstructive sleep apnea osteoarthritis osteoporosis pre-eclampsia primary biliary cholangitis renal cell carcinoma rhinitis short bowel syndrome steatotic liver disease type 2 diabetes mellitus
24536	leptin receptor	Lepr	arteriosclerosis chronic kidney disease chronic obstructive pulmonary disease congestive heart failure coronary artery disease diastolic heart failure dilated cardiomyopathy glucose intolerance hepatocellular carcinoma hepatocellular clear cell carcinoma human immunodeficiency virus infectious disease hyperglycemia hyperinsulinism hypertension metabolic dysfunction-associated steatohepatitis metabolic dysfunction-associated steatotic liver disease obesity obstructive sleep apnea osteoporosis pancreatitis pre-eclampsia primary biliary cholangitis proteinuria renal fibrosis short bowel syndrome sleep apnea type 2 diabetes mellitus
170905	LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	Lfng	spondylocostal dysostosis 3
246233	mono-ADP ribosylhydrolase 1	Macrod1
499751	mannosidase, alpha, class 1B, member 1	Man1b1	Rafiq syndrome
25478	mannosidase, alpha, class 2A, member 1	Man2a1	congenital dyserythropoietic anemia systemic lupus erythematosus
246136	mannosidase, alpha, class 2C, member 1	Man2c1
310864	mannosidase beta	Manba	beta-mannosidosis
140808	mannosidase, endo-alpha	Manea	anxiety disorder cocaine dependence panic disorder
683630	methionine adenosyltransferase 2 non-catalytic beta subunit	Mat2b
81829	malate dehydrogenase 2	Mdh2	brain ischemia congestive heart failure developmental and epileptic encephalopathy 51 myocardial infarction
315119	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	Mfng

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