{"symbol":"B9D1","synonyms":["JBTS27","EPPB9","MKSR1","MKS9"],"name":"B9 protein domain 1","description":"This gene encodes a B9 domain-containing protein, one of several that are involved in ciliogenesis. Alterations in expression of this gene have been found in a family with Meckel syndrome. Meckel syndrome has been associated with at least six different genes. This gene is located within the Smith-Magenis syndrome region on chromosome 17. [provided by RefSeq, Mar 2016]","ncbiEntrezGeneId":27077,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/27077","proteins":[{"symbol":"B9D1_HUMAN","href":"/api/1.0/protein/B9D1_HUMAN"}],"hgncRootFamilies":[]}