Literature DB >> 29891882

Biallelic variants in the ciliary gene TMEM67 cause RHYNS syndrome.

Francesco Brancati1,2, Letizia Camerota3, Emma Colao4, Virginia Vega-Warner5, Xiangzhong Zhao6, Ruixiao Zhang7, Irene Bottillo8, Marco Castori9, Alfredo Caglioti10, Federica Sangiuolo11, Giuseppe Novelli11, Nicola Perrotti12, Edgar A Otto13.   

Abstract

A rare syndrome was first described in 1997 in a 17-year-old male patient presenting with Retinitis pigmentosa, HYpopituitarism, Nephronophthisis and Skeletal dysplasia (RHYNS). In the single reported familial case, two brothers were affected, arguing for X-linked or recessive mode of inheritance. Up to now, the underlying genetic basis of RHYNS syndrome remains unknown. Here we applied whole-exome sequencing in the originally described family with RHYNS to identify compound heterozygous variants in the ciliary gene TMEM67. Sanger sequencing confirmed a paternally inherited nonsense c.622A > T, p.(Arg208*) and a maternally inherited missense variant c.1289A > G, p.(Asp430Gly), which perturbs the correct splicing of exon 13. Overall, TMEM67 showed one of the widest clinical continuum observed in ciliopathies ranging from early lethality to adults with liver fibrosis. Our findings extend the spectrum of phenotypes/syndromes resulting from biallelic TMEM67 variants to now eight distinguishable clinical conditions including RHYNS syndrome.

Entities:  

Mesh:

Substances:

Year:  2018        PMID: 29891882      PMCID: PMC6117343          DOI: 10.1038/s41431-018-0183-6

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


  20 in total

1.  The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat.

Authors:  Ursula M Smith; Mark Consugar; Louise J Tee; Brandy M McKee; Esther N Maina; Shelly Whelan; Neil V Morgan; Erin Goranson; Paul Gissen; Stacie Lilliquist; Irene A Aligianis; Christopher J Ward; Shanaz Pasha; Rachaneekorn Punyashthiti; Saghira Malik Sharif; Philip A Batman; Christopher P Bennett; C Geoffrey Woods; Carole McKeown; Martine Bucourt; Caroline A Miller; Phillip Cox; Lihadh Algazali; Richard C Trembath; Vicente E Torres; Tania Attie-Bitach; Deirdre A Kelly; Eamonn R Maher; Vincent H Gattone; Peter C Harris; Colin A Johnson
Journal:  Nat Genet       Date:  2006-01-15       Impact factor: 38.330

2.  Exome Sequencing and the Management of Neurometabolic Disorders.

Authors:  Maja Tarailo-Graovac; Casper Shyr; Colin J Ross; Gabriella A Horvath; Ramona Salvarinova; Xin C Ye; Lin-Hua Zhang; Amit P Bhavsar; Jessica J Y Lee; Britt I Drögemöller; Mena Abdelsayed; Majid Alfadhel; Linlea Armstrong; Matthias R Baumgartner; Patricie Burda; Mary B Connolly; Jessie Cameron; Michelle Demos; Tammie Dewan; Janis Dionne; A Mark Evans; Jan M Friedman; Ian Garber; Suzanne Lewis; Jiqiang Ling; Rupasri Mandal; Andre Mattman; Margaret McKinnon; Aspasia Michoulas; Daniel Metzger; Oluseye A Ogunbayo; Bojana Rakic; Jacob Rozmus; Peter Ruben; Bryan Sayson; Saikat Santra; Kirk R Schultz; Kathryn Selby; Paul Shekel; Sandra Sirrs; Cristina Skrypnyk; Andrea Superti-Furga; Stuart E Turvey; Margot I Van Allen; David Wishart; Jiang Wu; John Wu; Dimitrios Zafeiriou; Leo Kluijtmans; Ron A Wevers; Patrice Eydoux; Anna M Lehman; Hilary Vallance; Sylvia Stockler-Ipsiroglu; Graham Sinclair; Wyeth W Wasserman; Clara D van Karnebeek
Journal:  N Engl J Med       Date:  2016-05-25       Impact factor: 91.245

3.  Nephronophthisis.

Authors:  Shalabh Srivastava; John A Sayer
Journal:  J Pediatr Genet       Date:  2014-06

4.  Retinitis pigmentosa, growth hormone deficiency, and acromelic skeletal dysplasia in two brothers: possible familial RHYNS syndrome.

Authors:  P Hedera; J L Gorski
Journal:  Am J Med Genet       Date:  2001-06-15

5.  CELSR2, encoding a planar cell polarity protein, is a putative gene in Joubert syndrome with cortical heterotopia, microophthalmia, and growth hormone deficiency.

Authors:  Thierry Vilboux; May Christine V Malicdan; Joseph C Roney; Andrew R Cullinane; Joshi Stephen; Deniz Yildirimli; Joy Bryant; Roxanne Fischer; Meghana Vemulapalli; James C Mullikin; Peter J Steinbach; William A Gahl; Meral Gunay-Aygun
Journal:  Am J Med Genet A       Date:  2017-01-04       Impact factor: 2.802

6.  MKS3/TMEM67 mutations are a major cause of COACH Syndrome, a Joubert Syndrome related disorder with liver involvement.

Authors:  Francesco Brancati; Miriam Iannicelli; Lorena Travaglini; Annalisa Mazzotta; Enrico Bertini; Eugen Boltshauser; Stefano D'Arrigo; Francesco Emma; Elisa Fazzi; Romina Gallizzi; Mattia Gentile; Damir Loncarevic; Vlatka Mejaski-Bosnjak; Chiara Pantaleoni; Luciana Rigoli; Carmelo D Salpietro; Sabrina Signorini; Gilda Rita Stringini; Alain Verloes; Dominika Zabloka; Bruno Dallapiccola; Joseph G Gleeson; Enza Maria Valente
Journal:  Hum Mutat       Date:  2009-02       Impact factor: 4.878

7.  Evidence of oligogenic inheritance in nephronophthisis.

Authors:  Julia Hoefele; Matthias T F Wolf; John F O'Toole; Edgar A Otto; Ulla Schultheiss; Georges Dêschenes; Massimo Attanasio; Boris Utsch; Corinne Antignac; Friedhelm Hildebrandt
Journal:  J Am Soc Nephrol       Date:  2007-09-12       Impact factor: 10.121

8.  Molecular genetic findings and clinical correlations in 100 patients with Joubert syndrome and related disorders prospectively evaluated at a single center.

Authors:  Thierry Vilboux; Daniel A Doherty; Ian A Glass; Melissa A Parisi; Ian G Phelps; Andrew R Cullinane; Wadih Zein; Brian P Brooks; Theo Heller; Ariane Soldatos; Neal L Oden; Deniz Yildirimli; Meghana Vemulapalli; James C Mullikin; May Christine V Malicdan; William A Gahl; Meral Gunay-Aygun
Journal:  Genet Med       Date:  2017-01-26       Impact factor: 8.822

9.  The Meckel-Gruber Syndrome proteins MKS1 and meckelin interact and are required for primary cilium formation.

Authors:  Helen R Dawe; Ursula M Smith; Andrew R Cullinane; Dianne Gerrelli; Phillip Cox; Jose L Badano; Sarah Blair-Reid; Nisha Sriram; Nicholas Katsanis; Tania Attie-Bitach; Simon C Afford; Andrew J Copp; Deirdre A Kelly; Keith Gull; Colin A Johnson
Journal:  Hum Mol Genet       Date:  2006-12-21       Impact factor: 6.150

10.  Isolated congenital hepatic fibrosis associated with TMEM67 mutations: report of a new genotype-phenotype relationship.

Authors:  Ida Vogel; Peter Ott; Dorte Lildballe; Stephen Hamilton-Dutoit; Hendrik Vilstrup; Henning Grønbæk
Journal:  Clin Case Rep       Date:  2017-05-23
View more
  5 in total

1.  The Genomic Landscape of Sporadic Prolactinomas.

Authors:  Sunita M C De Sousa; Paul P S Wang; Stephen Santoreneos; Angeline Shen; Christopher J Yates; Milena Babic; Leila Eshraghi; Jinghua Feng; Barbara Koszyca; Samuel Roberts-Thomson; Andreas W Schreiber; David J Torpy; Hamish S Scott
Journal:  Endocr Pathol       Date:  2019-12       Impact factor: 3.943

2.  Novel compound heterozygous TMEM67 variants in a Vietnamese family with Joubert syndrome: a case report.

Authors:  Thi Phuong Hoa Bui; Ngoc Tu Nguyen; Van Doan Ngo; Hoai-Nghia Nguyen; Thi Thanh Ha Ly; Huy Duong Do; Minh-Tuan Huynh
Journal:  BMC Med Genet       Date:  2020-01-30       Impact factor: 2.103

Review 3.  Nephronophthisis-Pathobiology and Molecular Pathogenesis of a Rare Kidney Genetic Disease.

Authors:  Shabarni Gupta; Justyna E Ozimek-Kulik; Jacqueline Kathleen Phillips
Journal:  Genes (Basel)       Date:  2021-11-05       Impact factor: 4.096

4.  Refining Kidney Survival in 383 Genetically Characterized Patients With Nephronophthisis.

Authors:  Jens Christian König; Rebeka Karsay; Joachim Gerß; Karl-Peter Schlingmann; Mareike Dahmer-Heath; Anna-Katharina Telgmann; Sabine Kollmann; Gema Ariceta; Valentine Gillion; Detlef Bockenhauer; Aurélia Bertholet-Thomas; Antonio Mastrangelo; Olivia Boyer; Marc Lilien; Stéphane Decramer; Joost P Schanstra; Martin Pohl; Raphael Schild; Stefanie Weber; Julia Hoefele; Jens Drube; Metin Cetiner; Matthias Hansen; Julia Thumfart; Burkhard Tönshoff; Sandra Habbig; Max Christoph Liebau; Martin Bald; Carsten Bergmann; Petra Pennekamp; Martin Konrad
Journal:  Kidney Int Rep       Date:  2022-06-16

5.  Improving diagnosis for rare diseases: the experience of the Italian undiagnosed Rare diseases network.

Authors:  Marco Salvatore; Agata Polizzi; Maria Chiara De Stefano; Giovanna Floridia; Simone Baldovino; Dario Roccatello; Savino Sciascia; Elisa Menegatti; Giuseppe Remuzzi; Erica Daina; Paraskevas Iatropoulos; Bruno Bembi; Rosalia Maria Da Riol; Alessandra Ferlini; Marcella Neri; Giuseppe Novelli; Federica Sangiuolo; Francesco Brancati; Domenica Taruscio
Journal:  Ital J Pediatr       Date:  2020-09-14       Impact factor: 2.638

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.