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 **226 - 250** of **662** in total

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Gene ID	Gene Name ▼	Gene Symbol	Disease Ontology
140481	mannosidase 2, alpha 2	Man2a2	schizophrenia
17158	mannosidase 2, alpha 1	Man2a1	congenital dyserythropoietic anemia systemic lupus erythematosus
17155	mannosidase 1, alpha	Man1a
24070	mannose-P-dolichol utilization defect 1	Mpdu1	congenital disorder of glycosylation If
110119	mannose phosphate isomerase	Mpi	carbohydrate metabolic disorder congenital disorder of glycosylation Ib congenital disorder of glycosylation type I
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
69444	lysozyme-like 6	Lyzl6
69032	lysozyme-like 4	Lyzl4
67328	lysozyme-like 1	Lyzl1
332427	lysozyme G-like 2	Lyg2
69541	lysozyme G-like 1	Lyg1
17105	lysozyme 2	Lyz2	familial visceral amyloidosis
17110	lysozyme 1	Lyz1	familial visceral amyloidosis
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
110095	liver glycogen phosphorylase	Pygl	glycogen storage disease VI glycogen storage disease lactic acidosis
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
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

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