RHXF2 Polyclonal Antibody, 100ul Cell Dissociation Mutations in this gene are

Mutations in this gene are associated with neurofibromatosis type II which is characterized by nervous system and skin tumors and ocular abnormalities

DPYSL6 has been implicated in multiple neurological disorders

The 27 kDa form has no activity while the 22/25 kDa form can act as activator for collagenase

and is required for association with spectrin and actin

as well as X-linked combined immunodeficiency (XCID)

RHXF2 Polyclonal Antibody, 100ul Cell Dissociation Mutations in this gene areThis gene, which encodes a transcriptional repressor, is one of two paralogous X linked homeobox containing genes and is highly expressed in a variety of cancers. In addition, the encoded protein associates with the cell membrane and with microtubules, and is concentrated at the leading edge of migratory cells.