methylmalonyl-CoA epimerase
Ultimo aggiornamento 1 Jun 2021
Rispetta le linee guida editoriali
- ScaricaScarica
- Condividi
- Language
- Discussione
- Versione audio
- Aggiungi alle fonti preferite su Google
L MCEE gene provides instructions for making an enzyme called methylmalonyl CoA epimerase, which converts one form of the molecule methylmalonyl CoA to another. Specifically, the enzyme converts D-methylmalonyl CoA to L-methylmalonyl CoA. This conversion takes place within the pathway that converts the molecule propionyl-CoA to succinyl-CoA. This pathway is important in the breakdown of certain protein building blocks (amino acids), specific fats (lipids), and cholesterol.
Normal function
L MCEE gene provides instructions for making an enzyme called methylmalonyl CoA epimerase, which converts one form of the molecule methylmalonyl CoA to another. Specifically, the enzyme converts D-methylmalonyl CoA to L-methylmalonyl CoA. This conversion takes place within the pathway that converts the molecule propionyl-CoA to succinyl-CoA. This pathway is important in the breakdown of certain protein building blocks (amino acids), specific fats (lipids), and cholesterol.
Conditions referring to this gene or chromosome
Altri nomi
DL-methylmalonyl-CoA racemase
GLOD2
glyoxalase domain containing 2
MCEE_HUMAN
methylmalonyl CoA epimerase
methylmalonyl-CoA epimerase, mitochondrial
methylmalonyl-CoA epimerase, mitochondrial precursor
Related patient information and medicines

Patient information leaflet
Coartazione dell'aorta
How common is coarctation of the aorta. Congenital heart disease occurs in about 7 nel 1,000 pregnancies and coarctation of the aorta is just one type of congenital cardiache malattia. Around 1 in 2,500 babies have coarctation of the aorta. The condition is twice as common in males as it is in females and it is one of the more common congenital heart.

Medicine leaflet
Compresse di pravastatina
Over time, these patches can make a blood vessel narrower and this is called... The narrowing reduces the blood flow through the artery and increases the risk of a number of heart and blood vessel diseases, such as heart attack and stroke. Pravastatin belongs to a group of medicines known as statins (or HMG-CoA reductase inhibitors). It reduces.

Medicine leaflet
Compresse e capsule di fluvastatina
Fluvastatin belongs to a group of medicines known as statins. It regulates the amount of cholesterol and other lipids made by your body, and helps to reduce the risk of heart and blood vessel disease. The narrowing reduces the blood flow through the artery and increases the risk of a number of heart and blood vessel diseases, such a... Fluvastatin.

Medicine leaflet
Rosuvastatina
Rosuvastatina belongs to a group of medicines known as statins. It regulates ... About rosuvastatin Type of medicine A lipid-regulating medicine commonly known as a statin Used for Lowering cholesterol and other lipids in the blood; to reduce the risk of heart and blood vessel disease Also called Crestor® Available as Tablets and capsules Lipids,.

Medicine leaflet
Simvastatina
Simvastatina belongs to a group of medicines known as statins. Informazioni simvastatina Type of medicine A lipid-regulating medicine commonly known as a statin Used for Lowering cholesterol and other lipids in the blood; to reduce the risk of heart and blood vessel disease Also called Zocor®; Combination brand: Inegy® (simvastatin with ezetimibe ).

Medicine leaflet
Compresse di atorvastatina
Informazioni atorvastatina Type of medicine A lipid-regulating medicine commonly known as a statin Used for Lowering cholesterol and other lipids; to reduce the risk of heart and blood vessel disease Also called (UK) Lipitor® Also called (USA) Lipitor®; Combination brand: Caduet® (atorvastatin with amlodipine ) Available as Tablets and chewable tablets.
Ulteriori letture e riferimenti
- methylmalonyl-CoA epimerase; MedlinePlus, National Library of Medicine.
- Bikker H, Bakker HD, Abeling NG, Poll-The BT, Kleijer WJ, Rosenblatt DS, Waterham HR, Wanders RJ, Duran M. A homozygous nonsense mutation in the methylmalonyl-CoA epimerase gene (MCEE) results in mild methylmalonic aciduria. Hum Mutat. 2006 Jul;27(7):640-3. doi: 10.1002/humu.20373.
- Dobson CM, Gradinger A, Longo N, Wu X, Leclerc D, Lerner-Ellis J, Lemieux M, Belair C, Watkins D, Rosenblatt DS, Gravel RA. Homozygous nonsense mutation in the MCEE gene and siRNA suppression of methylmalonyl-CoA epimerase expression: a novel cause of mild methylmalonic aciduria. Mol Genet Metab. 2006 Aug;88(4):327-33. doi: 10.1016/j.ymgme.2006.03.009. Epub 2006 May 11.
- Gradinger AB, Belair C, Worgan LC, Li CD, Lavallee J, Roquis D, Watkins D, Rosenblatt DS. Atypical methylmalonic aciduria: frequency of mutations in the methylmalonyl CoA epimerase gene (MCEE). Hum Mutat. 2007 Oct;28(10):1045. doi: 10.1002/humu.9507.
Partecipa alla conversazione
Condividi i tuoi pensieri o esperienze con gli altri nel nostro comunità di pazienti.

Chiedi, condividi, connettiti.
Esplora le discussioni, fai domande e condividi esperienze su centinaia di argomenti di salute.
Iscriviti alla newsletter di Patient
La tua dose settimanale di consigli sulla salute chiari e affidabili - scritti per aiutarti a sentirti informato, sicuro e in controllo.
Abbonandoti accetti i nostri Informativa sulla Privacy. Puoi annullare l'iscrizione in qualsiasi momento. Non vendiamo mai i tuoi dati.