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 **101 - 125** of **662** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
15478	heparan sulfate (glucosamine) 3-O-sulfotransferase 3A1	Hs3st3a1
15531	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1	Ndst1	DiGeorge syndrome autism spectrum disorder autosomal recessive intellectual developmental disorder 46 azoospermia congenital diaphragmatic hernia intellectual disability newborn respiratory distress syndrome
15558	5-hydroxytryptamine (serotonin) 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
15586	hyaluronoglucosaminidase 1	Hyal1	mucopolysaccharidosis IX mucopolysaccharidosis pulmonary hypertension
15587	hyaluronoglucosaminidase 2	Hyal2	pulmonary hypertension
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
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
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
16182	interleukin 18 receptor 1	Il18r1	asthma hepatocellular carcinoma lung disease pulmonary fibrosis pulmonary sarcoidosis
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
16430	STT3, subunit of the oligosaccharyltransferase complex, homolog A (S. cerevisiae)	Stt3a	congenital disorder of glycosylation Iw
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
16592	fatty acid binding protein 5, epidermal	Fabp5	prostate cancer psoriasis
16770	lactalbumin, alpha	Lalba	gastroenteritis
16795	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
16828	lactate dehydrogenase A	Ldha	disease of metabolism hyperglycemia hypertension

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