{"symbol":"PEX13","synonyms":["PBD11A","PBD11B"],"name":"peroxisomal biogenesis factor 13","description":"This gene encodes a peroxisomal membrane protein that binds the type 1 peroxisomal targeting signal receptor via a SH3 domain located in the cytoplasm. Mutations and deficiencies in peroxisomal protein importing and peroxisome assembly lead to peroxisomal biogenesis disorders, an example of which is Zellweger syndrome. [provided by RefSeq, Oct 2008]","ncbiEntrezGeneId":5194,"ncbiEntrezGeneUrl":"http://www.ncbi.nlm.nih.gov/gene/5194","proteins":[{"symbol":"PEX13_HUMAN","href":"/api/1.0/protein/PEX13_HUMAN"}],"hgncRootFamilies":[]}