C3orf58: Difference between revisions
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{{infobox protein |name=chromosome 3 open reading frame 58 |caption= |image= |width= |HGNCid=28490 |Symbol=C3orf58 |AltSymbols= |EntrezGene=205428 |OMIM= |RefSeq=NM_173552 |UniProt= |PDB= |ECnumber= |Chromosome=3 |Arm=q |Band=24 |LocusSupplementaryData=}} | {{infobox protein |name=chromosome 3 open reading frame 58 |caption= |image= |width= |HGNCid=28490 |Symbol=C3orf58 |AltSymbols= |EntrezGene=205428 |OMIM= |RefSeq=NM_173552 |UniProt= |PDB= |ECnumber= |Chromosome=3 |Arm=q |Band=24 |LocusSupplementaryData=}} | ||
'''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|MEF2]] site binding proteins.<ref>{{cite journal | vauthors=Morrow EM, Yoo SY, Flavell SW |title=Identifying Autism Loci and Genes by Tracing Recent Shared Ancestry. |journal=Science |volume=321 |issue= 5886 |pages= 218–223 |year= 2008 |pmid= 18621663|doi= 10.1126/science.1157657 | pmc=2586171 |display-authors=etal}}</ref> | '''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|MEF2]] site [[Binding protein|binding proteins]].<ref>{{cite journal | vauthors=Morrow EM, Yoo SY, Flavell SW |title=Identifying Autism Loci and Genes by Tracing Recent Shared Ancestry. |journal=Science |volume=321 |issue= 5886 |pages= 218–223 |year= 2008 |pmid= 18621663|doi= 10.1126/science.1157657 | pmc=2586171 |display-authors=etal}}</ref> | ||
==See also== | ==See also== | ||
Latest revision as of 18:18, 16 February 2018
| chromosome 3 open reading frame 58 | |
|---|---|
| Identifiers | |
| Symbol | C3orf58 |
| Entrez | 205428 |
| HUGO | 28490 |
| RefSeq | NM_173552 |
| Other data | |
| Locus | Chr. 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]
See also
References
- ↑ 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.