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 **101 - 125** of **662** in total

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Gene ID	Gene Name	Gene Symbol	Disease Ontology ▲
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
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
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
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
216395	ribitol xylosyltransferase 1	Rxylt1	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A10
108902	beta-1,4-glucuronyltransferase 1	B4gat1	Walker-Warburg syndrome congenital muscular dystrophy-dystroglycanopathy type A13 muscular dystrophy-dystroglycanopathy type B1
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
241113	protein kinase, AMP-activated, gamma 3 non-catalytic subunit	Prkag3	Wolff-Parkinson-White syndrome lethal congenital glycogen storage disease of heart neurodegenerative disease
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
18293	oxoglutarate (alpha-ketoglutarate) dehydrogenase (lipoamide)	Ogdh	Yoon-Bellen neurodevelopmental syndrome oxoglutarate dehydrogenase deficiency
72774	nei endonuclease VIII-like 1 (E. coli)	Neil1	abdominal obesity-metabolic syndrome obesity
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
18609	pancreatic and duodenal homeobox 1	Pdx1	acute necrotizing pancreatitis cerebral infarction diabetes mellitus diabetic retinopathy hyperglycemia maturity-onset diabetes of the young type 4 maturity-onset diabetes of the young obesity pancreatic agenesis placental insufficiency type 1 diabetes mellitus type 2 diabetes mellitus
19662	retinol binding protein 4, plasma	Rbp4	acute pyelonephritis atherosclerosis cerebral infarction chronic kidney disease colon adenoma congestive heart failure coronary artery disease diabetic angiopathy diabetic retinopathy dilated cardiomyopathy essential hypertension familial hypercholesterolemia gallbladder cancer gestational diabetes hyperinsulinism hypertension liver cirrhosis myocardial infarction obesity pre-eclampsia proliferative diabetic retinopathy psoriasis severe pre-eclampsia systemic scleroderma type 2 diabetes mellitus
11821	adenine phosphoribosyl transferase	Aprt	adenine phosphoribosyltransferase deficiency hepatocellular carcinoma
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
50799	solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 13	Slc25a13	adult-onset type II citrullinemia citrullinemia common bile duct disease intrahepatic cholestasis neonatal-onset type II citrullinemia
18627	period circadian clock 2	Per2	advanced sleep phase syndrome 1 advanced sleep phase syndrome cocaine dependence
98660	ATPase, Na+/K+ transporting, alpha 2 polypeptide	Atp1a2	alcohol use disorder alternating hemiplegia of childhood benign neonatal seizures developmental and epileptic encephalopathy 98 epilepsy familial hemiplegic migraine 2 familial hemiplegic migraine hyperhomocysteinemia hypertension migraine with aura nervous system disease
232975	ATPase, Na+/K+ transporting, alpha 3 polypeptide	Atp1a3	alcohol use disorder alternating hemiplegia of childhood bipolar disorder developmental and epileptic encephalopathy 99 dystonia 12 epilepsy familial hemiplegic migraine nervous system disease
18166	neuropeptide Y receptor Y1	Npy1r	alcohol use disorder amphetamine abuse anxiety disorder childhood absence epilepsy cocaine abuse depressive disorder heroin dependence hypertension nicotine dependence obesity opiate dependence peripheral artery disease temporal lobe epilepsy visual epilepsy
30924	angiopoietin-like 3	Angptl3	alcohol use disorder familial hypobetalipoproteinemia 2
20440	beta galactoside alpha 2,6 sialyltransferase 1	St6gal1	alcohol use disorder high grade glioma
53412	protein phosphatase 1, regulatory subunit 3C	Ppp1r3c	alcohol use disorder type 2 diabetes mellitus

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