C3orf58

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
Symbol	C3orf58
NCBI gene	205428
HGNC	28490
RefSeq	NM_173552
Other data
Locus	Chr. 3 q24

See also

• Heritability of autism