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 **351 - 375** of **662** in total

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Gene ID	Gene Name	Gene Symbol ▲	Disease Ontology
14768	LanC (bacterial lantibiotic synthetase component C)-like 1	Lancl1
71835	LanC (bacterial lantibiotic synthetase component C)-like 2	Lancl2
236285	LanC lantibiotic synthetase component C-like 3 (bacterial)	Lancl3
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
228366	LARGE xylosyl- and glucuronyltransferase 2	Large2
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
16848	LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	Lfng	spondylocostal dysostosis 3
16889	lysosomal acid lipase A	Lipa	Wolman disease cholesterol ester storage disease lysosomal acid lipase deficiency
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
69541	lysozyme G-like 1	Lyg1
332427	lysozyme G-like 2	Lyg2
17110	lysozyme 1	Lyz1	familial visceral amyloidosis
17105	lysozyme 2	Lyz2	familial visceral amyloidosis
67328	lysozyme-like 1	Lyzl1
69032	lysozyme-like 4	Lyzl4
69444	lysozyme-like 6	Lyzl6
107227	mono-ADP ribosylhydrolase 1	Macrod1
72899	mono-ADP ribosylhydrolase 2	Macrod2
17155	mannosidase 1, alpha	Man1a
17156	mannosidase, alpha, class 1A, member 2	Man1a2
227619	mannosidase, alpha, class 1B, member 1	Man1b1	Rafiq syndrome
17158	mannosidase 2, alpha 1	Man2a1	congenital dyserythropoietic anemia systemic lupus erythematosus

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