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 **126 - 150** of **662** in total

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Gene ID ▲	Gene Name	Gene Symbol	Disease Ontology
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
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
17105	lysozyme 2	Lyz2	familial visceral amyloidosis
17110	lysozyme 1	Lyz1	familial visceral amyloidosis
17155	mannosidase 1, alpha	Man1a
17156	mannosidase, alpha, class 1A, member 2	Man1a2
17158	mannosidase 2, alpha 1	Man2a1	congenital dyserythropoietic anemia systemic lupus erythematosus
17159	mannosidase 2, alpha B1	Man2b1	alpha-mannosidosis
17160	mannosidase 2, alpha B2	Man2b2
17193	methyl-CpG binding domain protein 4	Mbd4	colorectal carcinoma esophagus squamous cell carcinoma lung cancer rheumatoid arthritis uveal melanoma
17254	solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2	Slc3a2	adenoid cystic carcinoma lung adenocarcinoma lung non-small cell carcinoma lung pleomorphic carcinoma stomach carcinoma tongue squamous cell carcinoma transitional cell carcinoma
17305	MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase	Mfng
17308	mannoside acetylglucosaminyltransferase 1	Mgat1
17309	mannoside acetylglucosaminyltransferase 3	Mgat3
17423	N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 2	Ndst2	autism spectrum disorder azoospermia intellectual disability
17425	forkhead box K1	Foxk1
17448	malate dehydrogenase 2, NAD (mitochondrial)	Mdh2	brain ischemia congestive heart failure developmental and epileptic encephalopathy 51 myocardial infarction
17449	malate dehydrogenase 1, NAD (soluble)	Mdh1	developmental and epileptic encephalopathy 88
17869	myelocytomatosis oncogene	Myc	Burkitt lymphoma acute lymphoblastic leukemia acute promyelocytic leukemia angiosarcoma breast cancer cancer chronic lymphocytic leukemia clear cell renal cell carcinoma coronary restenosis demyelinating disease hepatitis C hepatocellular carcinoma hyperparathyroidism leiomyoma liver cirrhosis lung adenocarcinoma lung cancer nephroblastoma obesity osteoporosis polycystic kidney disease 1 polycystic kidney disease prolactinoma prostate adenocarcinoma prostate cancer prostatic hypertrophy pulmonary hypertension renal cell carcinoma rhabdoid cancer thyroid gland papillary carcinoma urinary bladder cancer
17939	N-acetyl galactosaminidase, alpha	Naga	Fabry disease Kanzaki disease Schindler disease type 1 angiokeratoma neuroaxonal dystrophy
18010	neuraminidase 1	Neu1	glycoproteinosis mucolipidosis

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