PITX3 Polyclonal Antibody, 100ul Peripheral Blood Separation Tube Mutations in this gene have

Mutations in this gene have also been associated with a reduction in Plasmodium falciparum rosetting

It encodes a protein (adiponectin

dilated cardiomyopathy

Mutations in this gene have been associated with Kenny-Caffey syndrome (KCS) type 2 and the more severe osteocraniostenosis (OCS| also known as Gracile Bone Dysplasia)| both characterized by short stature| hypoparathyroidism| bone development abnormalities| and hypocalcemia

Isoforms Ialpha and Ibeta have identical cGMP-bindin

PITX3 Polyclonal Antibody, 100ul Peripheral Blood Separation Tube Mutations in this gene haveThis gene encodes a member of the RIEG PITX homeobox family, which is in the bicoid class of homeodomain proteins. Members of this family act as transcription factors. This protein is involved in lens formation during eye development. Mutations of this gene have been associated with anterior segment mesenchymal dysgenesis and congenital cataracts.