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
editReferences
edit- ^ 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.