C3orf58

{{Short description|Protein-coding gene in the species Homo sapiens}} {{cs1 config|name-list-style=vanc}} {{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.<ref>{{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 |bibcode=2008Sci...321..218M |display-authors=etal}}</ref>

==See also== * Heritability of autism

==References== {{reflist}}