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Autism Genetic Database

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.

URL: http://wren.bcf.ku.edu/

Resource ID: nlx_29034     Resource Type: Resource     Version: Latest Version



Additional Resource Types


Resource PubMed IDs

PMID: 19778453, PMID: 23281790


Autism Genetic Database: A comprehensive database for autism susceptibility gene-CNVs integrated with known noncoding RNAs and fragile sites

Funding Information

Autism Speaks, NIH, P20 RR0146475, 01.4506

Parent Organization

Curation Status




Resource Status

Last checked up;

Original Submitter


Version Status


Submitted On

12:00am May 26, 2011

Originated From


Changes from Previous Version

First Version

Version 1

Created 4 years ago by Anonymous