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{{infobox protein |name=chromosome 3 open reading frame 58 |caption= |image= |width= |HGNCid=28490 |Symbol=C3orf58 |AltSymbols= |EntrezGene=205428 |OMIM= |RefSeq=NM_173552 |UniProt= |PDB= |ECnumber= |Chromosome=3 |Arm=q |Band=24 |LocusSupplementaryData=}}C3orf58 is a human gene. It was highlighted in a screen for genes possibly related to autism. The authors propose that the gene should be renamed Deleted in autism-1 (DIA1). Experiments in a rat neuronal cell culture model suggested that this gene may be regulated directly or indirectly by MEF2 site binding proteins.[1]See alsoReferences1. ^{{cite journal | vauthors=Morrow EM, Yoo SY, Flavell SW |title=Identifying Autism Loci and Genes by Tracing Recent Shared Ancestry. |journal=Science |volume=321 |issue= 5886 |pages= 218–223 |year= 2008 |pmid= 18621663|doi= 10.1126/science.1157657 | pmc=2586171 |display-authors=etal}}
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