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 **601 - 625** of **662** in total

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Gene ID ▼	Gene Name	Gene Symbol	Disease Ontology
14422	beta-1,4-N-acetyl-galactosaminyl transferase 2	B4galnt2
14421	beta-1,4-N-acetyl-galactosaminyl transferase 1	B4galnt1	hereditary spastic paraplegia 26
14420	galactosylceramidase	Galc	Creutzfeldt-Jakob disease Krabbe disease Mycoplasma pneumoniae pneumonia melanoma
14387	glucosidase, alpha, acid	Gaa	glycogen storage disease II
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
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
14378	glucose-6-phosphatase, catalytic, 2	G6pc2
14377	glucose-6-phosphatase catalytic subunit 1	G6pc1	glycogen storage disease Ia hepatocellular carcinoma steatotic liver disease type 2 diabetes mellitus
14376	alpha glucosidase 2 alpha neutral subunit	Ganab	polycystic kidney disease 3 polycystic kidney disease polycystic liver disease
14348	fucosyltransferase 9	Fut9	candidiasis
14347	fucosyltransferase 7	Fut7	candidiasis
14345	fucosyltransferase 4	Fut4	candidiasis
14344	fucosyltransferase 2	Fut2	vitamin B12 deficiency
14343	fucosyltransferase 1	Fut1
14121	fructose bisphosphatase 1	Fbp1	fructose-1,6-bisphosphatase deficiency
14120	fructose bisphosphatase 2	Fbp2
14043	exostosin glycosyltransferase 2	Ext2	hereditary multiple exostoses
14042	exostosin glycosyltransferase 1	Ext1	autism spectrum disorder chondrosarcoma hereditary multiple exostoses
13853	epilepsy, progressive myoclonic epilepsy, type 2 gene alpha	Epm2a	Lafora disease progressive myoclonus epilepsy
13808	enolase 3, beta muscle	Eno3	aortic valve stenosis
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
13806	enolase 1, alpha non-neuron	Eno1	Alzheimer's disease hypertension
13481	dolichyl-phosphate mannosyltransferase subunit 2, regulatory	Dpm2	congenital disorder of glycosylation Iu congenital disorder of glycosylation type I
13480	dolichyl-phosphate mannosyltransferase subunit 1, catalytic	Dpm1	congenital disorder of glycosylation Ie congenital disorder of glycosylation type I
13478	dolichyl-phosphate N-acetylglucosaminephosphotransferase 1	Dpagt1	congenital disorder of glycosylation Ij congenital myasthenic syndrome 13

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