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SOX5

Protein-coding gene in Homo sapiens From Wikipedia, the free encyclopedia

SOX5
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Transcription factor SOX-5 is a protein that in humans is encoded by the SOX5 gene.[5][6]

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Function

This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. The encoded protein may play a role in chondrogenesis. A pseudogene of this gene is located on chromosome 8. Multiple transcript variants encoding distinct isoforms have been identified for this gene.[6]


Mutations in the SOX5 gene can cause Lamb-Shaffer syndrome.

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