VSX2 Polyclonal Antibody, 20ul Monoclonal Antibody Preparation Defects in this gene are

Defects in this gene are a cause of Walker-Warburg syndrome (WWS)

This protein plays a role in several cellular processes

This gene encodes the receptor for both luteinizing hormone and choriogonadotropin

at least one of which encodes a preproprotein that is proteolytically processed to generate heavy and light chains that form a disulfide-linked dimer

Members of the subfamily share similarity in sequence and splice sites

VSX2 Polyclonal Antibody, 20ul Monoclonal Antibody Preparation Defects in this gene areThis gene encodes a homeobox protein originally described as a retina specific transcription factor. Mutations in this gene are associated with microphthalmia, cataracts and iris abnormalities.