DPOG1 Polyclonal Antibody, 100ul Endonucleases & Exonucleases Mutations in INPP5D are associated

Mutations in INPP5D are associated with defects and cancers of the immune system

May play a role in cell proliferation of NT2 embryonal carcinoma cells

thus stabilizing the fibrin clot

This gene was identified as a potential candidate gene for obsessive-compulsive disorder in a genome-wide association study

This gene encodes an isoform of the alpha subunit of the elongation factor-1 complex

DPOG1 Polyclonal Antibody, 100ul Endonucleases & Exonucleases Mutations in INPP5D are associatedMitochondrial DNA polymerase is heterotrimeric, consisting of a homodimer of accessory subunits plus a catalytic subunit. The protein encoded by this gene is the catalytic subunit of mitochondrial DNA polymerase. The encoded protein contains a polyglutamine tract near its N terminus that may be polymorphic. Defects in this gene are a cause of progressive external ophthalmoplegia with mitochondrial DNA deletions 1 (PEOA1), sensory ataxic neuropathy