{"symbol":"RPGRIP1L","synonyms":["NPHP8","PPP1R134","CORS3","FTM","JBTS7","MKS5"],"name":"RPGRIP1-like","description":"The protein encoded by this gene can localize to the basal body-centrosome complex or to primary cilia and centrosomes in ciliated cells. The encoded protein has been found to interact with nephrocystin-4. Defects in this gene are a cause of Joubert syndrome type 7 (JBTS7) and Meckel syndrome type 5 (MKS5). [provided by RefSeq, Jun 2016]","ncbiEntrezGeneId":23322,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/23322","proteins":[{"symbol":"FTM_HUMAN","href":"/api/1.0/protein/FTM_HUMAN"}],"hgncRootFamilies":[{"name":"C2 domain containing","href":"/api/1.0/gene_family/C2+domain+containing"},{"name":"Protein phosphatase 1 regulatory subunits (PPP1R)","href":"/api/1.0/gene_family/Protein+phosphatase+1+regulatory+subunits+%28PPP1R%29"}]}