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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. Protein function: Plays a role in myoblast fusion, probable mediator of endocytic recycling for membrane trafficking events during myotube formation. [The UniProt Consortium]
Keywords:
Anti-FER1L5, Anti-Fer-1-like protein 5, FER1L5 Polyclonal Antibody
This website uses cookies, which are necessary for the technical operation of the website and are always set. Other cookies, which increase the usability of this website, serve for direct advertising or simplify interaction with other websites and social networks, will only be used with your consent.
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