{"symbol":"MEGF8","synonyms":["CRPT2","SBP1","C19ORF49","EGFL4"],"name":"multiple EGF-like-domains 8","description":"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. [provided by RefSeq, Dec 2012]","ncbiEntrezGeneId":1954,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/1954","proteins":[{"symbol":"MEGF8_HUMAN","href":"/api/1.0/protein/MEGF8_HUMAN"}],"hgncRootFamilies":[]}