| 1 | IPO13, JUN, KRT17 |
| Increased importin 13 activity is associated with the pathogenesis of pterygium. PMID: | |
| Xu K, Tao T, Jie J, Lu X, Li X, Mehmood MA, He H, Liu Z, Xiao X, Yang J, Ma JX, Li W, Zhou Y, Liu Z. | |
| Mol Vis. 2013;19:604-13. Epub 2013 Mar 20. 2013 | |
| 2 | KRT17 |
| Keratin 17 promotes epithelial proliferation and tumor growth by polarizing the immune response in skin. | |
| Depianto D, Kerns ML, Dlugosz AA, Coulombe PA. | |
| Nat Genet 42(10):910-4. Epub 2010 Sep 26. 2010 | |
| 3 | KRT17, PC217 |
| Recurrent mutation in keratin 17 in a large family with pachyonychia congenita type 2. | |
| Oh Adib C, Jones B, Liao H, Smith FJ, Solomon R, Egan CA, Leachman S. | |
| Arch Dermatol Res 300(5):211-4. Epub 2008 Mar 18. No abstract available. PMID: 18347808 2008 | |
| 4 | KRT17, PC217 |
| A novel point mutation of keratin 17 (KRT17) in a Japanese family with pachyonychia congenita type 2: an RNA-based genetic analysis using a single hair bulb. | |
| Tsuda T, Ishikawa C, Nakagawa N, Konishi H, Tarutani M, Matsuki M, Yamanishi K. | |
| Br J Dermatol 159(3):730-2. Epub 2008 Jun 28. No abstract available. PMID: 18547302 2008 | |
| 5 | KRT6A, KRT16, KRT17 |
| A spectrum of mutations in keratins K6a, K16 and K17 causing pachyonychia congenita. | |
| Liao H, Sayers JM, Wilson NJ, Irvine AD, Mellerio JE, Baselga E, Bayliss SJ, Uliana V, Fimiani M, Lane EB, McLean WH, Leachman SA, Smith FJ. | |
| J Dermatol Sci 48(3):199-205. Epub 2007 Aug 24. 2007 | |
| 6 | KRT17 |
| A keratin cytoskeletal protein regulates protein synthesis and epithelial cell growth. | |
| Kim S, Wong P, Coulombe PA. | |
| Nature 441(7091):362-5. 2006 | |
| 7 | KRT1, KRT10, KRT12, KRT13, KRT14, KRT14P, KRT15, KRT16, KRT17, KRT17P3, KRT18, KRT18P12, KRT18P16, KRT18P17, KRT18P18, KRT18P19, KRT18P20, KRT18P21, KRT18P22, KRT18P23, KRT18P24, KRT18P25, KRT18P26, KRT18P27, KRT18P28, KRT18P29, KRT18P30, KRT18P31, KRT18P32, KRT18P33, KRT18P34, KRT18P35, KRT18P36, KRT18P37, KRT18P38, KRT18P39, KRT18P40, KRT18P41, KRT18P42, KRT18P43, KRT18P44, KRT18P45, KRT18P46, KRT18P47, KRT18P48, KRT18P49, KRT18P5, KRT18P50, KRT18P8, KRT19, KRT19P1, KRT19P2, KRT19P3, KRT2, KRT20, KRT222, KRT23, KRT24, KRT25, KRT26, KRT27, KRT28, KRT3, KRT31, KRT32, KRT33, KRT33A, KRT34, KRT35, KRT36, KRT37, KRT38, KRT39, KRT4, KRT40, KRT5, KRT6A, KRT6B, KRT6C, KRT7, KRT71, KRT72, KRT73, KRT74, KRT75, KRT76, KRT77, KRT78, KRT79, KRT8, KRT80, KRT81, KRT82, KRT83, KRT84, KRT85, KRT86, KRT8P10, KRT8P13, KRT8P15, KRT8P17, KRT8P18, KRT8P19, KRT8P20, KRT8P21, KRT8P22, KRT8P23, KRT8P24, KRT8P25, KRT8P26, KRT8P27, KRT8P28, KRT8P29, KRT8P30, KRT8P5, KRT8P6, KRT8P7, KRT8P8, KRT8P9, KRT9, KRTAP19-8, KRTAP20-4 |
| New consensus nomenclature for mammalian keratins. | |
| Schweizer J, Bowden PE, Coulombe PA, Langbein L, Lane EB, Magin TM, Maltais L, Omary MB, Parry DA, Rogers MA, Wright MW. | |
| J Cell Biol 174(2):169-74. Epub 2006 Jul 10. 2006 | |
| 8 | KRT17, PC217 |
| A novel mutation in the second half of the keratin 17 1A domain in a large pedigree with delayed-onset pachyonychia congenita type 2. | |
| Xiao SX, Feng YG, Ren XR, Tan SS, Li L, Wang JM, Shi YZ. | |
| J Invest Dermatol 122(4):892-5. 2004 | |
| 9 | PC112, PC117, PC212, PC217, KRT17, KRT16, KRT6A |
| Novel and recurrent mutations in the genes encoding keratins K6a, K16 and K17 in 13 cases of pachyonychia congenita. | |
| Terrinoni A, Smith FJ, Didona B, Canzona F, Paradisi M, Huber M, Hohl D, David A, Verloes A, Leigh IM, Munro CS, Melino G, McLean WH. | |
| J Invest Dermatol 117(6):1391-6. 2001 | |
| 10 | PC217, KRT17 |
| Mutation report: identification of a germline mutation in keratin 17 in a family with pachyonychia congenita type 2. | |
| Celebi JT, Tanzi EL, Yao YJ, Michael EJ, Peacocke M. | |
| J Invest Dermatol 113(5):848-50 1999 | |
| 11 | PC217, KRT17 |
| Pachyonychia congenita type 2 : keratin 17 mutation in a Japanese case. | |
| Fujimoto W, et al. | |
| J Am Acad Dermatol 38 : 1007-1009. 1998 | |
| 12 | PC217, KRT17 |
| Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2. | |
| Covello SP, et al. | |
| Br J Dermatol 139 : 475-480. 1998 | |
| 13 | PC217, KRT17 |
| Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplex. | |
| Smith FJD, et al. | |
| J Invest Dermatol 108 : 220-223. 1997 | |
| 14 | KRT17, STM |
| Missense mutations in keratin 17 cause either pachyonychia congenita type 2 or a phenotype resembling steatocystoma multiplex. | |
| Smith FJ, Corden LD, Rugg EL, Ratnavel R, Leigh IM, Moss C, Tidman MJ, Hohl D, Huber M, Kunkeler L, Munro CS, Lane EB, McLean WH. | |
| J Invest Dermatol 108(2):220-3. 1997 | |
| 15 | KRT1@1, KRT19, KRT15, KRT17, KRT16, KRT14 |
| Close linkage of the two keratin gene clusters in the human genome. | |
| Milisavljevic V, Freedberg IM, Blumenberg M. | |
| Genomics 34(1):134-8. 1996 | |
| 16 | KRT16, PC117, PC217, KRT17 |
| Keratin 16 and keratin 17 mutations cause pachyonychia congenita. | |
| McLean WHI, et al. | |
| Nat Genet 9 : 273-278. 1995 | |
| 17 | KRT17 |
| A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21. | |
| Munro CS, et al. | |
| J Med Genet 31 : 675-678. 1994 | |