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・ Inosine nucleosidase
・ Inosine pranobex
・ Inosine-5′-monophosphate dehydrogenase
・ Inosinic acid
・ Inositol
・ Inositol (1,4,5) Trisphosphate-3- Kinase
・ Inositol 1-methyltransferase
・ Inositol 2-dehydrogenase
・ Inositol 3-alpha-galactosyltransferase
・ Inositol 3-kinase
・ Inositol 3-methyltransferase
・ Inositol 4-methyltransferase
・ Inositol monophosphatase
・ Inositol monophosphatase 1
・ Inositol monophosphatase 2
Inositol monophosphatase 3
・ Inositol nicotinate
・ Inositol oxygenase
・ Inositol pentakisphosphate
・ Inositol phosphate
・ Inositol theory of bipolar disorder
・ Inositol trisphosphate
・ Inositol trisphosphate receptor
・ Inositol-1,3,4-trisphosphate 5/6-kinase
・ Inositol-1,4-bisphosphate 1-phosphatase
・ Inositol-3-phosphate synthase
・ Inositol-hexakisphosphate kinase
・ Inositol-pentakisphosphate 2-kinase
・ Inositol-phosphate phosphatase
・ Inositol-polyphosphate 5-phosphatase


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Inositol monophosphatase 3 : ウィキペディア英語版
Inositol monophosphatase 3

Inositol monophosphatase 3 also known as inositol monophosphatase domain-containing protein 1 (IMPAD1) is an enzyme that in humans is encoded by the IMPAD1 gene.
This gene encodes a member of the inositol monophosphatase family. The encoded protein is localized to the Golgi apparatus and catalyzes the hydrolysis of phosphoadenosine phosphate (PAP) to adenosine monophosphate (AMP).〔
== Clinical significance ==

Mutations in this gene are a cause of GRAPP type chondrodysplasia with joint dislocations, and a pseudogene of this gene is located on the long arm of chromosome 1.
== References ==


抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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