F19A5 Polyclonal Antibody, 100ul Supplements Mutations in this gene cause

Mutations in this gene cause the immunodeficiency-centromeric instability-facial anomalies (ICF) syndrome

This protein is a secreted cytokine and growth regulator that inhibits the proliferation of a number of tumor cell lines

which heterodimerizes with MAX forming a transcriptional activation complex

such as Dejerine-Sottas syndrome (DSS) and congenital hypomyelinating neuropathy (CHN)

|PTM:Not phosphorylated

F19A5 Polyclonal Antibody, 100ul Supplements Mutations in this gene causeThis gene is a member of the TAFA family which is composed of five highly homologous genes that encode small secreted proteins. These proteins contain conserved cysteine residues at fixed positions, and are distantly related to MIP 1alpha, a member of the CC chemokine family. The TAFA proteins are predominantly expressed in specific regions of the brain, and are postulated to function as brain specific chemokines or neurokines that act as regulators