Dynein LC 1 Polyclonal Antibody, 50ul NGS Oligos Mutations in this gene have

Mutations in this gene have been associated with chronic granulomatous disease

An individual with autism and multiple exostoses was found to have a balanced translocation between chromosome 8 and a chromosome X breakpoint located within the gastrin-releasing peptide receptor gene

it is cleaved by complement factor D yielding the noncatalytic chain Ba and the catalytic subunit Bb

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a regulator of integrin mediated signaling

Dynein LC 1 Polyclonal Antibody, 50ul NGS Oligos Mutations in this gene haveDNAL1 encodes an axonemal dynein light chain which functions as a component of the outer dynein arms complex. This complex acts as the molecular motor that provides the force to move cilia in an ATP dependent manner. Dynein axonemal light chain 1 is expressed in tissues with motile cilia or flagella and may be involved in the movement of sperm flagella. Alternate splicing results in multiple transcript variants.