Literature DB >> 21567929

Mutation in SAM domain of TP63 is associated with nonsyndromic cleft lip and palate and cleft palate.

Piranit N Kantaputra1, Sutti Malaivijitnond, Alexandre R Vieira, Jan Heering, Volker Dötsch, Theerapong Khankasikum, Warissara Sripathomsawat.   

Abstract

Mutations in sterile alpha motif (SAM) domain of TP63 have been reported to be associated with ankyloblepharon-ectodermal dysplasia-cleft lip/palate syndrome and Rapp-Hodgkin syndrome. SAM domain, a protein-protein interaction module, is found in cytoplasmic signaling proteins and several transcriptional regulatory proteins which are involved in development and differentiation. Here, we report on a SAM domain mutation (p.Asp564His) in TP63 that predisposed the patients to have nonsyndromic cleft palate and nonsyndromic cleft lip and palate.
Copyright © 2011 Wiley-Liss, Inc.

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Year:  2011        PMID: 21567929     DOI: 10.1002/ajmg.a.34011

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.802


  4 in total

Review 1.  The evolution of human genetic studies of cleft lip and cleft palate.

Authors:  Mary L Marazita
Journal:  Annu Rev Genomics Hum Genet       Date:  2012-06-06       Impact factor: 8.929

2.  Analysis of large phenotypic variability of EEC and SHFM4 syndromes caused by K193E mutation of the TP63 gene.

Authors:  Jianhua Wei; Yang Xue; Lian Wu; Jie Ma; Xiuli Yi; Junrui Zhang; Bin Lu; Chunying Li; Dashuang Shi; Songtao Shi; Xinghua Feng; Tao Cai
Journal:  PLoS One       Date:  2012-05-04       Impact factor: 3.240

3.  Human cataract mutations in EPHA2 SAM domain alter receptor stability and function.

Authors:  Jeong Eun Park; Alexander I Son; Rui Hua; Lianqing Wang; Xue Zhang; Renping Zhou
Journal:  PLoS One       Date:  2012-05-03       Impact factor: 3.240

4.  Identification of a novel TP63 mutation causing nonsyndromic cleft lip with or without cleft palate.

Authors:  Tianhui Xu; Mengmeng Du; Xinhua Bu; Donglan Yuan; Zhiping Gu; Pei Yu; Xuefang Li; Jiao Chen; Chunyan Jin
Journal:  BMC Med Genomics       Date:  2021-02-23       Impact factor: 3.063

  4 in total

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