GlyCosmos Portal

Mus musculus (house mouse)

Summary

Taxonomy ID: 10090
PubChem Taxonomy: 10090

Genes (662) Glycans (1270) Glycoproteins (13000) Lectins (276) Pathways (1335)

Displaying entries **401 - 425** of **662** in total

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Gene ID	Gene Name ▲	Gene Symbol	Disease Ontology
16180	interleukin 1 receptor accessory protein	Il1rap
60367	interleukin 1 receptor accessory protein-like 2	Il1rapl2
16177	interleukin 1 receptor, type I	Il1r1	COVID-19 cholesteatoma of middle ear chronic recurrent multifocal osteomyelitis pulpitis severe acute respiratory syndrome systemic scleroderma type 1 diabetes mellitus
17082	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
107527	interleukin 1 receptor-like 2	Il1rl2
16182	interleukin 18 receptor 1	Il18r1	asthma hepatocellular carcinoma lung disease pulmonary fibrosis pulmonary sarcoidosis
16174	interleukin 18 receptor accessory protein	Il18rap
16195	interleukin 6 signal transducer	Il6st	Alzheimer's disease arteriosclerosis brain ischemia hepatocellular carcinoma hyper IgE recurrent infection syndrome 4 hyperandrogenism hypertension primary immunodeficiency disease rheumatoid arthritis status epilepticus stomach cancer visual epilepsy
15926	isocitrate dehydrogenase 1 (NADP+), soluble	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
269951	isocitrate dehydrogenase 2 (NADP+), mitochondrial	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
210973	kelch repeat and BTB (POZ) domain containing 2	Kbtbd2
16548	ketohexokinase	Khk	essential fructosuria
16591	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
83379	klotho beta	Klb	kidney disease
210808	laccase domain containing 1	Lacc1	juvenile rheumatoid arthritis
16770	lactalbumin, alpha	Lalba	gastroenteritis
235435	lactase-like	Lctl	kidney disease
16828	lactate dehydrogenase A	Ldha	disease of metabolism hyperglycemia hypertension
16846	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
16847	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
110095	liver glycogen phosphorylase	Pygl	glycogen storage disease VI glycogen storage disease lactic acidosis
16973	low density lipoprotein receptor-related protein 5	Lrp5	Worth syndrome autosomal dominant osteopetrosis 1 autosomal dominant polycystic kidney disease exudative vitreoretinopathy 4 exudative vitreoretinopathy heart valve disease idiopathic juvenile osteoporosis microphthalmia neovascular inflammatory vitreoretinopathy nonsyndromic deafness osteonecrosis osteoporosis-pseudoglioma syndrome osteoporosis polycystic liver disease tendinitis
16889	lysosomal acid lipase A	Lipa	Wolman disease cholesterol ester storage disease lysosomal acid lipase deficiency
17110	lysozyme 1	Lyz1	familial visceral amyloidosis
17105	lysozyme 2	Lyz2	familial visceral amyloidosis

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