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 **301 - 325** of **662** in total

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Gene ID	Gene Name	Gene Symbol ▼	Disease Ontology
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
16848	LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	Lfng	spondylocostal dysostosis 3
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
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
16828	lactate dehydrogenase A	Ldha	disease of metabolism hyperglycemia hypertension
235435	lactase-like	Lctl	kidney disease
228366	LARGE xylosyl- and glucuronyltransferase 2	Large2
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
236285	LanC lantibiotic synthetase component C-like 3 (bacterial)	Lancl3
71835	LanC (bacterial lantibiotic synthetase component C)-like 2	Lancl2
14768	LanC (bacterial lantibiotic synthetase component C)-like 1	Lancl1
16770	lactalbumin, alpha	Lalba	gastroenteritis
210808	laccase domain containing 1	Lacc1	juvenile rheumatoid arthritis
83379	klotho beta	Klb	kidney disease
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
16548	ketohexokinase	Khk	essential fructosuria
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
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
210973	kelch repeat and BTB (POZ) domain containing 2	Kbtbd2
18519	K(lysine) acetyltransferase 2B	Kat2b	breast cancer esophagus squamous cell carcinoma heart disease hepatocellular carcinoma kidney disease rheumatoid arthritis
14534	K(lysine) acetyltransferase 2A	Kat2a	heart disease kidney disease lung non-small cell carcinoma
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
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
16332	inositol polyphosphate phosphatase-like 1	Inppl1	hypertension obesity type 2 diabetes mellitus

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