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]

chromosome 3 open reading frame 58
Identifiers
SymbolC3orf58
NCBI gene205428
HGNC28490
RefSeqNM_173552
Other data
LocusChr. 3 q24

See also

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References

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  1. ^ Morrow EM, Yoo SY, Flavell SW, et al. (2008). "Identifying Autism Loci and Genes by Tracing Recent Shared Ancestry". Science. 321 (5886): 218–223. Bibcode:2008Sci...321..218M. doi:10.1126/science.1157657. PMC 2586171. PMID 18621663.