• 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...
    1 KB (94 words) - 03:16, 22 March 2024
  • Thumbnail for Heritability of autism
    implicated the following candidate genes: PCDH10, DIA1 (formerly known as C3ORF58), NHE9, CNTN3, SCN7A, and RNF8. Several of these genes appeared to be targets...
    113 KB (10,805 words) - 00:35, 5 August 2024
  • Thumbnail for CXorf36
    trigeminal ganglion tissue. CXorf36 has one paralog in humans known as C3orf58. Orthologs have been found in all mammals and through numerous eukaryotes...
    9 KB (1,100 words) - 22:48, 15 August 2023
  • genes have been linked to autism and autism spectrum disorders (ASD): c3orf58 (a.k.a. Deleted In Autism-1 or DIA1) and cXorf36 (a.k.a.Deleted in Autism-1...
    18 KB (1,992 words) - 21:12, 18 September 2024