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SOX18

Introduction

Transcription factor SOX-18 is a protein that in humans is encoded by the SOX18 gene.[1][2]

Function

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. This protein plays a role in hair, blood vessel, and lymphatic vessel development. Mutations in this gene have been associated with recessive and dominant forms of hypotrichosis–lymphedema–telangiectasia.[2]

Interactions

Interactions

SOX18 has been shown to interact with MEF2C.[3]

See also

See also

References

References

  1. ↑ Azuma T, Seki N, Yoshikawa T, Saito T, Masuho Y, Muramatsu M (July 2000). “cDNA cloning, tissue expression, and chromosome mapping of human homolog of SOX18”. J. Hum. Genet. 45 (3): 192–5. doi:10.1007/s100380050210. PMID 10807548.
  2. ↑ 2.0 2.1 “Entrez Gene: SO X18 SRY (sex determining region Y)-box 18”.
  3. ↑ Hosking BM, Wang SC, Chen SL, Penning S, Koopman P, Muscat GE (September 2001). “SOX18 directly interacts with MEF2C in endothelial cells”. Biochem. Biophys. Res. Commun. 287 (2): 493–500. doi:10.1006/bbrc.2001.5589. PMID 11554755.
Further reading

Further reading

External links

This article incorporates text from the United States National Library of Medicine, which is in the public domain.