{"symbol":"ANOS1","synonyms":["KMS","HHA","KALIG-1","KAL","KAL1","HH1","WFDC19","ADMLX"],"name":"anosmin 1","description":"Mutations in this gene cause the X-linked Kallmann syndrome. The encoded protein is similar in sequence to proteins known to function in neural cell adhesion and axonal migration. In addition, this cell surface protein is N-glycosylated and may have anti-protease activity. [provided by RefSeq, Jul 2008]","ncbiEntrezGeneId":3730,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/3730","proteins":[{"symbol":"KALM_HUMAN","href":"/api/1.0/protein/KALM_HUMAN"}],"hgncRootFamilies":[{"name":"WAP four-disulfide core domain containing (WFDC)","href":"/api/1.0/gene_family/WAP+four-disulfide+core+domain+containing+%28WFDC%29"},{"name":"Fibronectin type III domain containing","href":"/api/1.0/gene_family/Fibronectin+type+III+domain+containing"}]}