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C3orf58 information


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


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]

  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.

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C3orf58

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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...

Word Count : 94

Heritability of autism

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implicated the following candidate genes: PCDH10, DIA1 (formerly known as C3ORF58), NHE9, CNTN3, SCN7A, and RNF8. Several of these genes appeared to be targets...

Word Count : 10803

CXorf36

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trigeminal ganglion tissue. CXorf36 has one paralog in humans known as C3orf58. Orthologs have been found in all mammals and through numerous eukaryotes...

Word Count : 1100

Cognitive genomics

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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...

Word Count : 1995

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