Protein wntless homolog explained

Protein wntless homolog, commonly known as Wntless, is encoded in humans by the WLS gene .[1] Wntless is a receptor for Wnt proteins in Wnt-secreting cells.[2]

Wntless was shown to be a cargo for the retromer complex. It has been found essential for hair follicle induction.[3]

A homozygous missense mutation in the WLS gene was identified in Zaki syndrome.[4]

Further reading

Notes and References

  1. Web site: WLS - Protein wntless homolog - Homo sapiens (Human) - WLS gene & protein . www.uniprot.org . 30 May 2022 . en.
  2. Eaton S . Retromer retrieves wntless . Developmental Cell . 14 . 1 . 4–6 . January 2008 . 18194646 . 10.1016/j.devcel.2007.12.014 . free .
  3. Fu J, Hsu W . Epidermal Wnt controls hair follicle induction by orchestrating dynamic signaling crosstalk between the epidermis and dermis . The Journal of Investigative Dermatology . 133 . 4 . 890–898 . April 2013 . 23190887 . 3594635 . 10.1038/jid.2012.407 .
  4. Chai G, Szenker-Ravi E, Chung C, Li Z, Wang L, Khatoo M, Marshall T, Jiang N, Yang X, McEvoy-Venneri J, Stanley V, Anzenberg P, Lang N, Wazny V, Yu J, Virshup DM, Nygaard R, Mancia F, Merdzanic R, Toralles MB, Pitanga PM, Puri RD, Hernan R, Chung WK, Bertoli-Avella AM, Al-Sannaa N, Zaki MS, Willert K, Reversade B, Gleeson JG . A Human Pleiotropic Multiorgan Condition Caused by Deficient Wnt Secretion . The New England Journal of Medicine . 385 . 14 . 1292–1301 . September 2021 . 34587386 . 9017221 . 10.1056/NEJMoa2033911 .