Description
Product Characteristics: FER1L5 (Fer-1 Like Family Member 5) is a Protein Coding gene. Diseases associated with FER1L5 include Miyoshi Muscular Dystrophy and Deafness, Autosomal Recessive 9. An important paralog of this gene is DYSF.
Target Information: Plays a role in myoblast fusion, probable mediator of endocytic recycling for membrane trafficking events during myotube formation. {ECO:0000269:PubMed:21177873}