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Welcome to the Newly Redesigned SFARI GeneLearn 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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Animal 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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Protein Interactions

The Protein Interaction (PIN) module of SFARI Gene is an interactive visual reference that showcases all known protein interactions of gene products associated with ASD.

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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 on all known CNVs associated with ASD.

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About SFARI Gene

SFARI Gene is a publicly available, professionally curated, and searchable database for the autism research community.

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881 Total scored genes

2172 Total CNV loci

1342 Total Animal Models

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