{"symbol":"FANCB","synonyms":["FAAP90","FAAP95","FAB","FACB","FA2"],"name":"Fanconi anemia, complementation group B","description":"This gene encodes a member of the Fanconi anemia complementation group B. This protein is assembled into a nucleoprotein complex that is involved in the repair of DNA lesions. Mutations in this gene can cause chromosome instability and VACTERL syndrome with hydrocephalus. [provided by RefSeq, Apr 2016]","ncbiEntrezGeneId":2187,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/2187","proteins":[{"symbol":"FANCB_HUMAN","href":"/api/1.0/protein/FANCB_HUMAN"}],"hgncRootFamilies":[{"name":"Fanconi anemia, complementation groups (FANC)","href":"/api/1.0/gene_family/Fanconi+anemia%2C+complementation+groups+%28FANC%29"}]}