MY18B Polyclonal Antibody, 50ul Cell Separation and Collection Certain defects in this gene

Certain defects in this gene have been associated with the degenerative eye disease retinitis pigmentosa

Several alternatively spliced transcripts encoding different isoforms

ATXN7L3 localizes to nucleus and contains one SCA7 domain and one SGF11-type zinc finger

neurophysin 2 and copeptin

MY18B Polyclonal Antibody, 50ul Cell Separation and Collection Certain defects in this geneThe protein encoded by this gene may regulate muscle specific genes when in the nucleus and may influence intracellular trafficking when in the cytoplasm. The encoded protein functions as a homodimer and may interact with F actin. Mutations in this gene are associated with lung cancer.