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Resource:Autism Genetic Database
| Name: | Resource:Autism Genetic Database |
| Description: | The Autism Genetic Database currently contains the full list of autism susceptibility genes as well as all Copy Number Variations (CNVs) found to have a relationship to autism. Additionally, all noncoding RNA molecules (snoRNA, miRNA, and piRNA) and chemically induced fragile sites are stored as well. This information is currently accessible via an in-house human genome browser focusing specifically on the chromosomal features associated with autism, and in a tabular format broken down by chromosome.
Genome Browser:A genome browser that displays the genes, CNVs, ncRNAs and fragile sites in an easily accessible graphical visualization tool Tabular Data Display:A tabular data display that allows the user to observe the chromosomal spatial relationship between the genes, CNVs, ncRNAs and fragile sites. This also provides links to Entrez and pubmed for each gene, as well as miRBase for miRNAs, snoRNA-LBME-db for snoRNAs, and piRNABank for piRNAs. |
| Other Name(s): | Autism Genetic Database: A comprehensive database for autism susceptibility gene-CNVs integrated with known noncoding RNAs and fragile sites |
| Parent Organization: | University of Kansas; Kansas; USA |
| Supporting Agency: | National Institutes of Health, Resource:Autism Speaks |
| Resource Type(s): | Database |
| Grant: | P20 RR0146475, 01.4506 |
| Abbreviation: | AGD |
| Resource: | Resource |
| URL: | http://wren.bcf.ku.edu/ |
| PMID: | PMID 19778453 |
| Id: | nlx_29034 |
| Link to OWL / RDF: | Download this content as OWL/RDF |
Curation status: Curated
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Facts about Resource:Autism Genetic DatabaseRDF feed
| Abbrev | AGD + |
| CurationStatus | uncurated + |
| DefiningCitation | http://wren.bcf.ku.edu/ + |
| Definition | The Autism Genetic Database currently cont … The Autism Genetic Database currently contains the full list of autism susceptibility genes as well as all Copy Number Variations (CNVs) found to have a relationship to autism. Additionally, all noncoding RNA molecules (snoRNA, miRNA, and piRNA) and chemically induced fragile sites are stored as well. This information is currently accessible via an in-house human genome browser focusing specifically on the chromosomal features associated with autism, and in a tabular format broken down by chromosome.
Genome Browser:A genome browser that displays the genes, CNVs, ncRNAs and fragile sites in an easily accessible graphical visualization tool Tabular Data Display:A tabular data display that allows the user to observe the chromosomal spatial relationship between the genes, CNVs, ncRNAs and fragile sites. This also provides links to Entrez and pubmed for each gene, as well as miRBase for miRNAs, snoRNA-LBME-db for snoRNAs, and piRNABank for piRNAs. -db for snoRNAs, and piRNABank for piRNAs. |
| Grant | Category:P20 RR0146475 +, and Category:01.4506 + |
| Has default formThis property is a special property in this wiki. | Resource + |
| Has role | Database + |
| Id | nlx_29034 + |
| Is part of | University of Kansas; Kansas; USA + |
| Label | Resource:Autism Genetic Database + |
| ModifiedDate | 26 May 2011 + |
| PMID | 19778453 + |
| Page has default formThis property is a special property in this wiki. | Resource + |
| SuperCategory | Resource + |
| Supporting Agency | National Institutes of Health +, and Resource:Autism Speaks + |
| Synonym | Autism Genetic Database: A comprehensive database for autism susceptibility gene-CNVs integrated with known noncoding RNAs and fragile sites + |