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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: Uncurated

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Contributors

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Facts about Resource:Autism Genetic DatabaseRDF feed
AbbrevAGD  +
CurationStatusuncurated  +
DefiningCitationhttp://wren.bcf.ku.edu/  +
DefinitionThe 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.
GrantCategory:P20 RR0146475   +, and Category:01.4506   +
Has default formThis property is a special property in this wiki.Resource  +
Has roleDatabase  +
Idnlx_29034  +
Is part ofUniversity of Kansas; Kansas; USA  +
LabelResource:Autism Genetic Database  +
ModifiedDate26 May 2011  +
PMID19778453  +
Page has default formThis property is a special property in this wiki.Resource  +
SuperCategoryResource  +
Supporting AgencyNational Institutes of Health  +, and Resource:Autism Speaks  +
SynonymAutism Genetic Database: A comprehensive database for autism susceptibility gene-CNVs integrated with known noncoding RNAs and fragile sites  +