NCBI Description of MEGF8
|The protein encoded by this gene is a single-pass type I membrane protein of unknown function that contains several EGF-like domains, Kelch repeats, and PSI domains. Defects in this gene are a cause of Carpenter syndrome 2. Two transcript variants encoding different isoforms have been found for this gene.|
Community Annotation of MEGF8 Add / Edit MEGF8: Annotations
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