FoxD4 Polyclonal Antibody, 50ul Lysosome Mutations in this gene can

Mutations in this gene can result in vitamin D-dependent rickets type I

Probably is operated by a phosphatidylinositol second messenger system activated by receptor tyrosine kinases or G-protein coupled receptors

Defects in this gene are a cause of progressive external ophthalmoplegia with mitochondrial DNA deletions 1 (PEOA1)

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FoxD4 Polyclonal Antibody, 50ul Lysosome Mutations in this gene canFOXD4 encodes a member of the forkhead winged helix box (FOX) family of transcription factors. FOX transcription factors play critical roles in the regulation of multiple processes including metabolism, cell proliferation and gene expression during ontogenesis. Mutations in this gene are associated with a complex phenotype consisting of dilated cardiomyopathy, obsessive compulsive disorders, and suicidality.