RASL10B Polyclonal Antibody, 100ul Filtration A mutation in this gene

A mutation in this gene is associated with autosomal dominant cerebral ataxia

The deletion of a portion of the long (q) arm of human chromosome 7 is associated with Williams-Beuren syndrome

LIM domain kinase 1 is ubiquitously expressed during development and plays a role in many cellular processes associated with cytoskeletal structure

The protein is localized to the outer limiting membrane in the retina| and is thought to function in photoreceptor polarity and the organization of specialized intercellular junctions

It associates with polyribosomes

RASL10B Polyclonal Antibody, 100ul Filtration A mutation in this geneRASL10B (RAS Like Family 10 Member B) is a Protein Coding gene. GO annotations related to this gene include GTP binding. An important paralog of this gene is RASL10A.