# C3orf58

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> Source: https://en.wikipedia.org/wiki/C3orf58
> Source revision: 1214936002
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{{Short description|Protein-coding gene in the species Homo sapiens}}
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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](/source/gene). It was highlighted in a screen for genes possibly related to [autism](/source/autism). The authors propose that the gene should be renamed Deleted in autism-1 (DIA1). Experiments in a rat neuronal [cell culture](/source/cell_culture) model suggested that this gene may be regulated directly or indirectly by [MEF2](/source/Mef2) site [binding proteins](/source/Binding_protein).<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](/source/Heritability_of_autism)

==References==
{{reflist}}

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Adapted from the Wikipedia article [C3orf58](https://en.wikipedia.org/wiki/C3orf58) by Wikipedia contributors ([contributor history](https://en.wikipedia.org/wiki/C3orf58?action=history)). Available under [Creative Commons Attribution-ShareAlike 4.0 International](https://creativecommons.org/licenses/by-sa/4.0/). Changes may have been made.