ApoA-V Polyclonal Antibody, 100ul Reagent Reservoirs Mutations in this gene are

Mutations in this gene are associated with Schmid type metaphyseal chondrodysplasia (SMCD) and Japanese type spondylometaphyseal dysplasia (SMD)

Transcription factor that plays an important role in cellular development and cell survival

Protein phosphatase-1 (PP1) is one of the main eukaryotic serine/threonine phosphatases

) leading to the fusion of this gene and the FBLN1 gene is found in a complex type of synpolydactyly

ApoA-V Polyclonal Antibody, 100ul Reagent Reservoirs Mutations in this gene areThe apolipoprotein A5 by APOA5 is an apolipoprotein that plays an important role in regulating the plasma triglyceride levels, a major risk factor for coronary artery disease. It is a component of high density lipoprotein and is highly similar to a rat protein that is upregulated in response to liver injury. Mutations in this gene have been associated with hypertriglyceridemia and hyperlipoproteinemia type 5. This gene is located proximal to the