{"symbol":"NAGA","synonyms":["GALB","D22S674"],"name":"N-acetylgalactosaminidase, alpha-","description":"NAGA encodes the lysosomal enzyme alpha-N-acetylgalactosaminidase, which cleaves alpha-N-acetylgalactosaminyl moieties from glycoconjugates. Mutations in NAGA have been identified as the cause of  Schindler disease types I and II (type II also known as Kanzaki disease). [provided by RefSeq, Jul 2008]","ncbiEntrezGeneId":4668,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/4668","proteins":[{"symbol":"NAGAB_HUMAN","href":"/api/1.0/protein/NAGAB_HUMAN"}],"hgncRootFamilies":[]}