LBX1 Polyclonal Antibody, 50ul Plasmid Preparation Mutations in this gene or

Mutations in this gene or in the enhancer regions can cause ocular disorders such as aniridia and Peter's anomaly

The encoded protein may function as a transcription factor

may play a role in actin remodeling

Translocation of nucleotide sugars from the cytosol into the lumen compartment is mediated by specific nucleotide sugar transporters| such as SLC35D2 (Suda et al

LBX1 Polyclonal Antibody, 50ul Plasmid Preparation Mutations in this gene orThis gene and the orthologous mouse gene were found by their homology to the Drosophila lady bird early and late homeobox genes. In the mouse, this gene is a key regulator of muscle precursor cell migration and is required for the acquisition of dorsal identities of forelimb muscles.