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 **326 - 350** of **662** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
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
75731	idnK gluconokinase homolog (E. coli)	Idnk
15937	immediate early response 3	Ier3	T-cell non-Hodgkin lymphoma
16002	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
16182	interleukin 18 receptor 1	Il18r1	asthma hepatocellular carcinoma lung disease pulmonary fibrosis pulmonary sarcoidosis
16174	interleukin 18 receptor accessory protein	Il18rap
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
16180	interleukin 1 receptor accessory protein	Il1rap
60367	interleukin 1 receptor accessory protein-like 2	Il1rapl2
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
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
16332	inositol polyphosphate phosphatase-like 1	Inppl1	hypertension obesity type 2 diabetes mellitus
16333	insulin I	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
16334	insulin II	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
14534	K(lysine) acetyltransferase 2A	Kat2a	heart disease kidney disease lung non-small cell carcinoma
18519	K(lysine) acetyltransferase 2B	Kat2b	breast cancer esophagus squamous cell carcinoma heart disease hepatocellular carcinoma kidney disease rheumatoid arthritis
210973	kelch repeat and BTB (POZ) domain containing 2	Kbtbd2
16514	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
16535	potassium voltage-gated channel, subfamily Q, member 1	Kcnq1	Beckwith-Wiedemann syndrome Jervell-Lange Nielsen syndrome atrial fibrillation familial atrial fibrillation heart conduction disease hypertension long QT syndrome 1 long QT syndrome seminoma short QT syndrome type 2 diabetes mellitus
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

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