Literature DB >> 18270537

Sequence analysis of 21 genes located in the Kartagener syndrome linkage region on chromosome 15q.

Maciej Geremek1, Frederieke Schoenmaker, Ewa Zietkiewicz, Andrzej Pogorzelski, Scott Diehl, Cisca Wijmenga, Michal Witt.   

Abstract

Primary ciliary dyskinesia (PCD) is a rare genetic disorder, which shows extensive genetic heterogeneity and is mostly inherited in an autosomal recessive fashion. There are four genes with a proven pathogenetic role in PCD. DNAH5 and DNAI1 are involved in 28 and 10% of PCD cases, respectively, while two other genes, DNAH11 and TXNDC3, have been identified as causal in one PCD family each. We have previously identified a 3.5 cM (2.82 Mb) region on chromosome 15q linked to Kartagener syndrome (KS), a subtype of PCD characterized by the randomization of body organ positioning. We have now refined the KS candidate region to a 1.8 Mb segment containing 18 known genes. The coding regions of these genes and three neighboring genes were subjected to sequence analysis in seven KS probands, and we were able to identify 60 single nucleotide sequence variants, 35 of which resided in mRNA coding sequences. However, none of the variations alone could explain the occurrence of the disease in these patients.

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Year:  2008        PMID: 18270537     DOI: 10.1038/ejhg.2008.5

Source DB:  PubMed          Journal:  Eur J Hum Genet        ISSN: 1018-4813            Impact factor:   4.246


  8 in total

1.  Clinical and genetic analysis of a family with Kartagener syndrome caused by novel DNAH5 mutations.

Authors:  Xuan Xu; Ping Gong; Jie Wen
Journal:  J Assist Reprod Genet       Date:  2016-12-17       Impact factor: 3.412

2.  Ciliopathy with special emphasis on kartageners syndrome.

Authors:  Ashfaq Ul Hassan; Ghulam Hassan; Sajad Hamid Khan; Zahida Rasool; Afeera Abida
Journal:  Int J Health Sci (Qassim)       Date:  2009-01

3.  Identifying the role of transient receptor potential channels (TRPs) in kidney renal clear cell carcinoma and their potential therapeutic significances using genomic and transcriptome analyses.

Authors:  Jie Ren; Qihang Yuan; Jifeng Liu; Lei Zhong; Hanshuo Li; Guangzhen Wu; Feng Chen; Qizhen Tang
Journal:  BMC Med Genomics       Date:  2022-07-13       Impact factor: 3.622

4.  Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia.

Authors:  Christina Austin-Tse; Jan Halbritter; Maimoona A Zariwala; Renée M Gilberti; Heon Yung Gee; Nathan Hellman; Narendra Pathak; Yan Liu; Jennifer R Panizzi; Ramila S Patel-King; Douglas Tritschler; Raqual Bower; Eileen O'Toole; Jonathan D Porath; Toby W Hurd; Moumita Chaki; Katrina A Diaz; Stefan Kohl; Svjetlana Lovric; Daw-Yang Hwang; Daniela A Braun; Markus Schueler; Rannar Airik; Edgar A Otto; Margaret W Leigh; Peadar G Noone; Johnny L Carson; Stephanie D Davis; Jessica E Pittman; Thomas W Ferkol; Jeffry J Atkinson; Kenneth N Olivier; Scott D Sagel; Sharon D Dell; Margaret Rosenfeld; Carlos E Milla; Niki T Loges; Heymut Omran; Mary E Porter; Stephen M King; Michael R Knowles; Iain A Drummond; Friedhelm Hildebrandt
Journal:  Am J Hum Genet       Date:  2013-10-03       Impact factor: 11.025

5.  Mutations in radial spoke head protein genes RSPH9 and RSPH4A cause primary ciliary dyskinesia with central-microtubular-pair abnormalities.

Authors:  Victoria H Castleman; Leila Romio; Rahul Chodhari; Robert A Hirst; Sandra C P de Castro; Keith A Parker; Patricia Ybot-Gonzalez; Richard D Emes; Stephen W Wilson; Colin Wallis; Colin A Johnson; Rene J Herrera; Andrew Rutman; Mellisa Dixon; Amelia Shoemark; Andrew Bush; Claire Hogg; R Mark Gardiner; Orit Reish; Nicholas D E Greene; Christopher O'Callaghan; Saul Purton; Eddie M K Chung; Hannah M Mitchison
Journal:  Am J Hum Genet       Date:  2009-02-05       Impact factor: 11.025

6.  The highly conserved FOXJ1 target CFAP161 is dispensable for motile ciliary function in mouse and Xenopus.

Authors:  Anja Beckers; Franziska Fuhl; Tim Ott; Karsten Boldt; Magdalena Maria Brislinger; Peter Walentek; Karin Schuster-Gossler; Jan Hegermann; Leonie Alten; Elisabeth Kremmer; Adina Przykopanski; Katrin Serth; Marius Ueffing; Martin Blum; Achim Gossler
Journal:  Sci Rep       Date:  2021-06-25       Impact factor: 4.379

Review 7.  Management of primary ciliary dyskinesia/Kartagener's syndrome in infertile male patients and current progress in defining the underlying genetic mechanism.

Authors:  Yan-Wei Sha; Lu Ding; Ping Li
Journal:  Asian J Androl       Date:  2014 Jan-Feb       Impact factor: 3.285

8.  Genomic profiling supports the diagnosis of primary ciliary dyskinesia and reveals novel candidate genes and genetic variants.

Authors:  Marina Andjelkovic; Predrag Minic; Misa Vreca; Maja Stojiljkovic; Anita Skakic; Aleksandar Sovtic; Milan Rodic; Vesna Skodric-Trifunovic; Nina Maric; Jelena Visekruna; Vesna Spasovski; Sonja Pavlovic
Journal:  PLoS One       Date:  2018-10-09       Impact factor: 3.240

  8 in total

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