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 **251 - 275** of **662** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▼
12654	chitinase 3 like 1	Chi3l1	acute myeloid leukemia arteriosclerosis asthma bacterial meningitis breast cancer bronchopulmonary dysplasia chondrosarcoma chronic obstructive pulmonary disease colorectal carcinoma congestive heart failure coronary artery disease endometrial cancer glioblastoma hypertension lung non-small cell carcinoma melanoma multiple myeloma myocardial infarction ovarian cancer pre-eclampsia prostate carcinoma pulmonary fibrosis pulmonary sarcoidosis rheumatoid arthritis schizophrenia small cell carcinoma systemic scleroderma temporal arteritis type 1 diabetes mellitus type 2 diabetes mellitus
72774	nei endonuclease VIII-like 1 (E. coli)	Neil1	abdominal obesity-metabolic syndrome obesity
18293	oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide)	Ogdh	Yoon-Bellen neurodevelopmental syndrome oxoglutarate dehydrogenase 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
16889	lysosomal acid lipase A	Lipa	Wolman disease cholesterol ester storage disease lysosomal acid lipase deficiency
241113	protein kinase, AMP-activated, gamma 3 non-catalytic subunit	Prkag3	Wolff-Parkinson-White syndrome lethal congenital glycogen storage disease of heart neurodegenerative disease
108099	protein kinase, AMP-activated, gamma 2 non-catalytic subunit	Prkag2	Wolff-Parkinson-White syndrome glycogen storage disease hypertrophic cardiomyopathy 6 lethal congenital glycogen storage disease of heart neurodegenerative disease
108902	beta-1,4-glucuronyltransferase 1	B4gat1	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A13 muscular dystrophy-dystroglycanopathy type B1
216395	ribitol xylosyltransferase 1	Rxylt1	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A10
68273	protein O-linked mannose beta 1,2-N-acetylglucosaminyltransferase	Pomgnt1	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2O congenital muscular dystrophy-dystroglycanopathy type A3 lissencephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B3 muscular dystrophy retinitis pigmentosa
217734	protein-O-mannosyltransferase 2	Pomt2	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2N autosomal recessive limb-girdle muscular dystrophy congenital muscular dystrophy-dystroglycanopathy type A2 lissencephaly muscular dystrophy-dystroglycanopathy type B2 muscular dystrophy-dystroglycanopathy muscular dystrophy
99011	protein-O-mannosyltransferase 1	Pomt1	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2K cardiomyopathy cleft lip congenital muscular dystrophy-dystroglycanopathy type A1 lissencephaly muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy muscular dystrophy
243853	fukutin related protein	Fkrp	Walker-Warburg syndrome autosomal recessive limb-girdle muscular dystrophy type 2I congenital muscular dystrophy-dystroglycanopathy type A5 dilated cardiomyopathy limb-girdle muscular dystrophy muscular dystrophy-dystroglycanopathy type B1 muscular dystrophy-dystroglycanopathy type B5 muscular dystrophy
59048	C1GALT1-specific chaperone 1	C1galt1c1	Tn polyagglutination syndrome hemolytic-uremic syndrome
15211	hexosaminidase A	Hexa	Tay-Sachs disease
15937	immediate early response 3	Ier3	T-cell non-Hodgkin lymphoma
218989	transmembrane protein 260	Tmem260	T-cell non-Hodgkin lymphoma non-Hodgkin lymphoma stomach cancer
110006	glucuronidase, beta	Gusb	Sly syndrome mucopolysaccharidosis peritonitis
15212	hexosaminidase B	Hexb	Sandhoff disease lysosomal storage disease spinal muscular atrophy
227619	mannosidase, alpha, class 1B, member 1	Man1b1	Rafiq syndrome
14380	glucose-6-phosphate dehydrogenase 2	G6pd2	Plasmodium falciparum malaria anemia cataract cerebrovascular disease cholestasis congenital hypothyroidism congenital nonspherocytic hemolytic anemia diabetes mellitus favism hemolytic anemia hepatic encephalopathy hepatocellular carcinoma hyperhomocysteinemia kidney disease malaria metabolic dysfunction-associated steatotic liver disease myocardial infarction neonatal jaundice obesity phenylketonuria renovascular hypertension transient cerebral ischemia type 1 diabetes mellitus type 2 diabetes mellitus
14381	glucose-6-phosphate dehydrogenase X-linked	G6pdx	Plasmodium falciparum malaria anemia cataract cerebrovascular disease cholestasis congenital hypothyroidism congenital nonspherocytic hemolytic anemia diabetes mellitus favism hemolytic anemia hepatic encephalopathy hepatocellular carcinoma hyperhomocysteinemia kidney disease malaria metabolic dysfunction-associated steatotic liver disease myocardial infarction neonatal jaundice obesity phenylketonuria renovascular hypertension transient cerebral ischemia type 1 diabetes mellitus type 2 diabetes mellitus
381694	beta-3-glucosyltransferase	B3glct	Peters plus syndrome
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
13807	enolase 2, gamma neuronal	Eno2	Parkinsonism brain disease breast carcinoma hypertension migraine without aura neuroendocrine carcinoma prostate cancer toxic shock syndrome urinary bladder cancer visual epilepsy

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