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SFARI Gene release notes for Q2 2020Learn More

Human Gene

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).

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Gene Scoring

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.

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Mouse Models

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.

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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.

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Database updated on September 16, 2020

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SFARI Gene Update

We are pleased to announce some changes to the ongoing curation of the data in SFARI Gene. In the context of a continued effort to develop the human gene module and its manually curated list of autism risk genes, we are modifying other aspects of the site to focus on the information that is of greatest interest to the research community. The version of SFARI Gene that has been developed until now will be frozen and will remain available as “SFARI Gene Archive”. Please see the announcement for more details.
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