FoxO4 Polyclonal Antibody, 50ul[BT-AP03337] Cell Separation and Collection Mutations in this gene cause

Mutations in this gene cause ribose 5-phosphate isomerase deficiency

cardiac muscle 1) belongs to the actin family which is comprised of three main groups of actin isoforms

is located in the mitochondria and expressed in extra-hepatic tissues

a craniofacial development disorder

This gene encodes a member of the group 2 decarboxylase family

FoxO4 Polyclonal Antibody, 50ul[BT-AP03337] Cell Separation and Collection Mutations in this gene causeFOXO4 encodes a member of the O class of winged helix forkhead transcription factor family. Proteins encoded by this class are regulated by factors involved in growth and differentiation indicating they play a role in these processes. A translocation involving this gene on chromosome X and the homolog of the Drosophila trithorax gene, encoding a DNA binding protein, located on chromosome 11 is associated with leukemia. Multiple transcript variants