Literature DB >> 15832313

TCOF1 mutation database: novel mutation in the alternatively spliced exon 6A and update in mutation nomenclature.

Alessandra Splendore1, Roberto D Fanganiello, Cibele Masotti, Lucas S C Morganti, M Rita Passos-Bueno.   

Abstract

Recently, a novel exon was described in TCOF1 that, although alternatively spliced, is included in the major protein isoform. In addition, most published mutations in this gene do not conform to current mutation nomenclature guidelines. Given these observations, we developed an online database of TCOF1 mutations in which all the reported mutations are renamed according to standard recommendations and in reference to the genomic and novel cDNA reference sequences (www.genoma.ib.usp.br/TCOF1_database). We also report in this work: 1) results of the first screening for large deletions in TCOF1 by Southern blot in patients without mutation detected by direct sequencing; 2) the identification of the first pathogenic mutation in the newly described exon 6A; and 3) statistical analysis of pathogenic mutations and polymorphism distribution throughout the gene.

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Year:  2005        PMID: 15832313     DOI: 10.1002/humu.20159

Source DB:  PubMed          Journal:  Hum Mutat        ISSN: 1059-7794            Impact factor:   4.878


  16 in total

1.  Gross deletions in TCOF1 are a cause of Treacher-Collins-Franceschetti syndrome.

Authors:  Michael Bowman; Michael Oldridge; Caroline Archer; Anthony O'Rourke; Joanna McParland; Roel Brekelmans; Anneke Seller; Tracy Lester
Journal:  Eur J Hum Genet       Date:  2012-02-08       Impact factor: 4.246

Review 2.  Rare syndromes of the head and face: mandibulofacial and acrofacial dysostoses.

Authors:  Karla Terrazas; Jill Dixon; Paul A Trainor; Michael J Dixon
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2017-02-10       Impact factor: 5.814

3.  Mutation screening of Chinese Treacher Collins syndrome patients identified novel TCOF1 mutations.

Authors:  Ying Chen; Luo Guo; Chen-Long Li; Jing Shan; Hai-Song Xu; Jie-Ying Li; Shan Sun; Shao-Juan Hao; Lei Jin; Gang Chai; Tian-Yu Zhang
Journal:  Mol Genet Genomics       Date:  2017-12-11       Impact factor: 3.291

4.  First Report of a Single Exon Deletion in TCOF1 Causing Treacher Collins Syndrome.

Authors:  J Beygo; K Buiting; S Seland; H-J Lüdecke; U Hehr; C Lich; B Prager; D R Lohmann; D Wieczorek
Journal:  Mol Syndromol       Date:  2012-01-26

5.  Reduced TCOF1 mRNA level in a rhesus macaque with Treacher Collins-like syndrome: further evidence for haploinsufficiency of treacle as the cause of disease.

Authors:  Kathryn H Shows; Christy Ward; Laura Summers; Lin Li; Gregory R Ziegler; Andrew G Hendrickx; Rita Shiang
Journal:  Mamm Genome       Date:  2006-02-07       Impact factor: 2.957

6.  Regulation of the mouse Treacher Collins syndrome homolog (Tcof1) promoter through differential repression of constitutive expression.

Authors:  Kathryn H Shows; Rita Shiang
Journal:  DNA Cell Biol       Date:  2008-11       Impact factor: 3.311

7.  Novel mutations of TCOF1 gene in European patients with Treacher Collins syndrome.

Authors:  Chiara Conte; Maria Rosaria D'Apice; Fabrizio Rinaldi; Stefano Gambardella; Federica Sangiuolo; Giuseppe Novelli
Journal:  BMC Med Genet       Date:  2011-09-27       Impact factor: 2.103

8.  Fishing the molecular bases of Treacher Collins syndrome.

Authors:  Andrea M J Weiner; Nadia L Scampoli; Nora B Calcaterra
Journal:  PLoS One       Date:  2012-01-25       Impact factor: 3.240

9.  Genome analysis of the domestic dog (Korean Jindo) by massively parallel sequencing.

Authors:  Ryong Nam Kim; Dae-Soo Kim; Sang-Haeng Choi; Byoung-Ha Yoon; Aram Kang; Seong-Hyeuk Nam; Dong-Wook Kim; Jong-Joo Kim; Ji-Hong Ha; Atsushi Toyoda; Asao Fujiyama; Aeri Kim; Min-Young Kim; Kun-Hyang Park; Kang Seon Lee; Hong-Seog Park
Journal:  DNA Res       Date:  2012-04-03       Impact factor: 4.458

10.  Reduced transcription of TCOF1 in adult cells of Treacher Collins syndrome patients.

Authors:  Cibele Masotti; Camila C Ornelas; Alessandra Splendore-Gordonos; Ricardo Moura; Têmis M Félix; Nivaldo Alonso; Anamaria A Camargo; Maria Rita Passos-Bueno
Journal:  BMC Med Genet       Date:  2009-12-14       Impact factor: 2.103

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