SFARI Gene is an evolving database for the autism research community that is centered on genes implicated in autism susceptibility.
Announcing the New SFARI Gene and Gene ArchiveLearn More
The Human Gene module provides researchers around the world with instant access to the most up-to-date information on all known human genes associated with autism spectrum disorders (ASD).Explore the Database
New genetic links to autism are being discovered every day. To more accurately assess potential genetic causes, SFARI Gene assigns every gene in the database with a score reflecting the strength of the evidence linking it to the development of autism.Explore Gene Scoring
By including data from various animal models, the SFARI Gene database provides researchers with valuable information that can be used to help identify underlying mechanisms of ASD and ultimately improve treatments.Explore Mouse Models
Copy Number Variants
Copy number variation is considered to be one of the leading genetic causes of ASD. SFARI Gene’s Copy Number Variant (CNV) module provides users with data and ongoing curation for a select set of recurrent CNVs, and access to CNV calls for the Simons Simplex Collection.Explore CNVs