MOX-2 Polyclonal Antibody, 50ul Cell Function Analysis Mutations in this gene are

Mutations in this gene are associated with arthrogryposis-renal dysfunction-cholestasis syndrome

IGLL1 encodes one of the surrogate light chain subunits and is a member of the immunoglobulin gene superfamily

Two alternatively spliced transcript variants encoding different isoforms are described for this gene

also have C-terminal regions that share homology with neurotrophin receptors (see NTRK1

MOX-2 Polyclonal Antibody, 50ul Cell Function Analysis Mutations in this gene areMEOX2 encodes a member of a subfamily of non clustered, diverged, antennapedia like homeobox containing genes. Homeobox protein MOX 2 may play a role in the regulation of vertebrate limb myogenesis. Mutations in the related mouse protein may be associated with craniofacial and or skeletal abnormalities, in addition to neurovascular dysfunction observed in Alzheimer's disease.