Keratin 17 Explained

Keratin, type I cytoskeletal 17 is a protein that in humans is encoded by the KRT17 gene.[1] [2] [3] [4]

Keratin 17 is a type I cytokeratin. It is found in nail beds, hair follicles, sebaceous glands, and other epidermal appendages. Mutations in the gene encoding this protein lead to PC-K17 (previously known as Jackson-Lawler) type pachyonychia congenita and steatocystoma multiplex.

Interactions

Keratin 17 has been shown to interact with CCDC85B.[5]

Further reading

External links

Notes and References

  1. McLean WH, Rugg EL, Lunny DP, Morley SM, Lane EB, Swensson O, Dopping-Hepenstal PJ, Griffiths WA, Eady RA, Higgins C . Keratin 16 and keratin 17 mutations cause pachyonychia congenita . Nat Genet . 9 . 3 . 273–8 . Jul 1995 . 7539673 . 10.1038/ng0395-273 . 1873772 .
  2. Troyanovsky SM, Leube RE, Franke WW . Characterization of the human gene encoding cytokeratin 17 and its expression pattern . Eur J Cell Biol . 59 . 1 . 127–37 . Jan 1993 . 1281771 .
  3. Schweizer J, Bowden PE, Coulombe PA, Langbein L, Lane EB, Magin TM, Maltais L, Omary MB, Parry DA, Rogers MA, Wright MW . New consensus nomenclature for mammalian keratins . J Cell Biol . 174 . 2 . 169–74 . Jul 2006 . 16831889 . 2064177 . 10.1083/jcb.200603161 .
  4. Web site: Entrez Gene: KRT17 keratin 17.
  5. Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, Berriz GF, Gibbons FD, Dreze M, Ayivi-Guedehoussou N, Klitgord N, Simon C, Boxem M, Milstein S, Rosenberg J, Goldberg DS, Zhang LV, Wong SL, Franklin G, Li S, Albala JS, Lim J, Fraughton C, Llamosas E, Cevik S, Bex C, Lamesch P, Sikorski RS, Vandenhaute J, Zoghbi HY, Smolyar A, Bosak S, Sequerra R, Doucette-Stamm L, Cusick ME, Hill DE, Roth FP, Vidal M . Towards a proteome-scale map of the human protein-protein interaction network . . 437 . 7062 . 1173–8 . Oct 2005 . 16189514 . 10.1038/nature04209 . 2005Natur.437.1173R . 4427026 .