AUTS2
Protein-coding gene in the species Homo sapiens
AUTS2, activator of transcription and developmental regulator is a protein that in humans is encoded by the AUTS2 gene.
01Function
This gene has been implicated in neurodevelopment and as a candidate gene for numerous neurological disorders, including autism spectrum disorders, intellectual disability, and developmental delay. Mutations in this gene have also been associated with non-neurological disorders, such as acute lymphoblastic leukemia, aging of the skin, early-onset androgenetic alopecia, and certain cancers.
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This article is adapted from the Wikipedia article “AUTS2”, written by its contributors and licensed under CC BY-SA 4.0. Fathomly has changed the layout, removed citation markers, navigation and maintenance notices, and adjusted punctuation. This adapted version is shared under the same license. For references, see the original article.
Images, from Wikimedia Commons:
- Ideogram human chromosome 7.svg by National Center for Biotechnology Information, U.S. National Library of Medicine, Public domain
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