Biology:SOX5

From HandWiki
Short description: Protein-coding gene in Homo sapiens


A representation of the 3D structure of the protein myoglobin showing turquoise α-helices.
Generic protein structure example

Transcription factor SOX-5 is a protein that in humans is encoded by the SOX5 gene.[1][2]

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.[2]


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

See also

  • SOX genes

References

  1. "Cloning and characterization of SOX5, a new member of the human SOX gene family". Genomics 36 (2): 354–8. Sep 1996. doi:10.1006/geno.1996.0474. PMID 8812465. 
  2. 2.0 2.1 "Entrez Gene: SOX5 SRY (sex determining region Y)-box 5". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=6660. 

Further reading