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Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.

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C3orf58

Introduction


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]

See also

See also

References

References

  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. doi:10.1126/science.1157657. PMC 2586171. PMID 18621663.