Mevalonate kinase is an enzyme (specifically a kinase) that in humans is encoded by the MVK gene. Mevalonate kinases are found in a wide variety of ...
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Oct 1, 2018 · Mevalonate kinase deficiency is a condition characterized by recurrent episodes of fever, which typically begin during infancy.
Mevalonate kinase
Protein
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Mevalonate kinase is an enzyme that in humans is encoded by the MVK gene. Mevalonate kinases are found in a wide variety of organisms from bacteria to mammals. This enzyme catalyzes the following reaction:
. Wikipedia
Gene Ontology: AmiGO / QuickGO
Jul 20, 2016 · Mevalonate kinase deficiency (MKD) is a recessively inherited autoinflammatory disorder with a spectrum of manifestations, including the ...
Mevalonate kinase is a peroxisomal enzyme that catalyzes the conversion of mevalonic acid to 5-phosphomevalonic acid in the synthesis of sterols (i.e., ...
6 days ago · This gene encodes the peroxisomal enzyme mevalonate kinase. Mevalonate is a key intermediate, and mevalonate kinase a key early enzyme, ...
Sep 9, 2021 · Mevalonate kinase deficiency (MKD) is a rare genetic autoinflammatory disorder. Autoinflammatory syndromes are a group of disorders ...
Mevalonate kinase deficiency (MKD) is an autosomal recessive metabolic disorder that disrupts the biosynthesis of cholesterol and isoprenoids.
Jun 5, 2020 · Mevalonate kinase deficiency is an autosomal recessive inborn error of metabolism. Bi-allelic mutations in the gene mevalonate kinase (MVK) lead ...
A rare inborn error of metabolism characterized by a spectrum of presentation ranging from hyperimmunoglobulinemia D with periodic fever (HIDS) to mevalonic ...
Mevalonate kinase deficiency is a disorder in the presqualene cholesterol biosynthetic pathway, characterized by recurrent inflammatory symptoms such as ...