{"symbol":"FRAS1","synonyms":["FRASRS1"],"name":"Fraser extracellular matrix complex subunit 1","description":"This gene encodes an extracellular matrix protein that appears to function in the regulation of epidermal-basement membrane adhesion and organogenesis during development. Mutations in this gene cause Fraser syndrome, a multisystem malformation that can include craniofacial, urogenital and respiratory system abnormalities. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]","ncbiEntrezGeneId":80144,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/80144","proteins":[{"symbol":"FRAS1_HUMAN","href":"/api/1.0/protein/FRAS1_HUMAN"}],"hgncRootFamilies":[]}