SOX18

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Template:Short description An Error has occurred retrieving Wikidata item for infobox Transcription factor SOX-18 is a protein that in humans is encoded by the SOX18 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. 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 (HLTS).[3][2] An autosomal truncating dominant mutation in this gene has also been associated with renal failure in the condition hypotrichosis-lymphedema-telangiectasia-renal defect syndrome (HLTRS).[4][5]

Interactions

SOX18 has been shown to interact with:

MEF2C[6]

RBPJ[7]

See also

References

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  1. ^ Page Module:Citation/CS1/styles.css has no content.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". Journal of Human Genetics. 45 (3): 192–5. doi:10.1007/s100380050210. PMID 10807548.
  2. ^ a b Page Module:Citation/CS1/styles.css has no content."Entrez Gene: SO X18 SRY (sex determining region Y)-box 18".
  3. ^ Page Module:Citation/CS1/styles.css has no content.Valenzuela I, Fernández-Alvarez P, Plaja A, Ariceta G, Sabaté-Rotés A, García-Arumí E, Vendrell T, Tizzano E (May 2018). "Further delineation of the SOX18-related Hypotrichosis, Lymphedema, Telangiectasia syndrome (HTLS)". European Journal of Medical Genetics. 61 (5): 269–272. doi:10.1016/j.ejmg.2018.01.001. PMID 29307792.
  4. ^ Page Module:Citation/CS1/styles.css has no content.Moalem S, Brouillard P, Kuypers D, Legius E, Harvey E, Taylor G, Francois M, Vikkula M, Chitayat D (April 2015). "Hypotrichosis-lymphedema-telangiectasia-renal defect associated with a truncating mutation in the SOX18 gene". Clinical Genetics. 87 (4): 378–82. doi:10.1111/cge.12388. PMID 24697860. S2CID 32417398.
  5. ^ Page Module:Citation/CS1/styles.css has no content."Hypotrichosis-Lymphedema-Telangiectasia-Renal Defect Syndrome". The University of Arizona Health Sciences.
  6. ^ Page Module:Citation/CS1/styles.css has no content.Hosking BM, Wang SC, Chen SL, Penning S, Koopman P, Muscat GE (September 2001). "SOX18 directly interacts with MEF2C in endothelial cells". Biochemical and Biophysical Research Communications. 287 (2): 493–500. Bibcode:2001BBRC..287..493H. doi:10.1006/bbrc.2001.5589. PMID 11554755.
  7. ^ Page Module:Citation/CS1/styles.css has no content.Overman J, Fontaine F, Wylie-Sears J, Moustaqil M, Huang L, Meurer M, et al. (July 2019). "R-propranolol is a small molecule inhibitor of the SOX18 transcription factor in a rare vascular syndrome and hemangioma". eLife. 8 e43026. doi:10.7554/eLife.43026. PMC 6667216. PMID 31358114.

Further reading

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

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