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 **301 - 325** of **449** in total

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Gene ID	Gene Name ▲	Gene Symbol	Disease Ontology
25694	hyaluronan synthase 2	Has2	diabetes insipidus middle cerebral artery infarction pulmonary hypertension
266805	hyaluronan synthase 3	Has3	pulmonary hypertension
367166	hyaluronidase 1	Hyal1	mucopolysaccharidosis IX mucopolysaccharidosis pulmonary hypertension
300993	hyaluronidase 3	Hyal3
24465	hypoxanthine phosphoribosyltransferase 1	Hprt1	HRPT-related hyperuricemia Lesch-Nyhan syndrome hepatocellular carcinoma
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
24483	insulin-like growth factor 2	Igf2	Alzheimer's disease Lewy body dementia Parkinson's disease Silver-Russell syndrome acquired immunodeficiency syndrome alcohol use disorder alcoholic neuropathy brain infarction breast cancer choriocarcinoma congenital diaphragmatic hernia congenital disorder of glycosylation Ia gastrointestinal system disease hepatocellular carcinoma inflammatory bowel disease liver cirrhosis meningitis multiple sclerosis multiple system atrophy osteoarthritis osteoporosis rheumatoid arthritis type 1 diabetes mellitus type 2 diabetes mellitus ulcerative colitis ventricular septal defect
25685	insulin-like growth factor binding protein 1	Igfbp1	breast cancer diabetic angiopathy
25466	interleukin 1 receptor accessory protein	Il1rap
317553	interleukin 1 receptor accessory protein-like 1	Il1rapl1	intellectual disability non-syndromic X-linked intellectual disability 21
25556	interleukin 1 receptor-like 1	Il1rl1	Hantavirus hemorrhagic fever with renal syndrome Human papillomavirus infectious disease acute myocardial infarction asthma bacterial pneumonia chronic obstructive pulmonary disease coronary artery disease hemolytic-uremic syndrome idiopathic pulmonary fibrosis paracoccidioidomycosis rhinitis tongue squamous cell carcinoma
171106	interleukin 1 receptor-like 2	Il1rl2
24476	islet amyloid polypeptide	Iapp	type 1 diabetes mellitus type 2 diabetes mellitus
24479	isocitrate dehydrogenase (NADP(+)) 1	Idh1	D-2-hydroxyglutaric aciduria acute myeloid leukemia autoimmune disease cancer glioblastoma hepatocellular clear cell carcinoma high grade glioma lung adenocarcinoma lung squamous cell carcinoma myelodysplastic syndrome
361596	isocitrate dehydrogenase (NADP(+)) 2	Idh2	D-2-hydroxyglutaric aciduria 2 acute myeloid leukemia bone remodeling disease esophagus squamous cell carcinoma hepatocellular carcinoma hepatocellular clear cell carcinoma high grade glioma intrahepatic cholangiocarcinoma lung adenocarcinoma lung cancer lung non-small cell carcinoma lung squamous cell carcinoma status epilepticus stomach cancer
25659	ketohexokinase	Khk	essential fructosuria
24528	lactalbumin, alpha	Lalba	gastroenteritis
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
81829	malate dehydrogenase 2	Mdh2	brain ischemia congestive heart failure developmental and epileptic encephalopathy 51 myocardial infarction
300741	mannose phosphate isomerase	Mpi	carbohydrate metabolic disorder congenital disorder of glycosylation Ib congenital disorder of glycosylation type I
303244	mannose-P-dolichol utilization defect 1	Mpdu1	congenital disorder of glycosylation If

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