{"symbol":"HPDL","synonyms":["4-HPPD-L","GLOXD1"],"name":"4-hydroxyphenylpyruvate dioxygenase-like","description":"The protein encoded by this intronless gene localizes to mitochondria, where it may function as 4-hydroxyphenylpyruvate dioxygenase. Clinical studies have identified several bi-allelic variants in this gene that lower the level of the encoded protein and lead to a clinically variable form of pediatric-onset spastic movement disorder. [provided by RefSeq, Aug 2020]","ncbiEntrezGeneId":84842,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/84842","proteins":[{"symbol":"HPDL_HUMAN","href":"/api/1.0/protein/HPDL_HUMAN"}],"hgncRootFamilies":[]}