Literature DB >> 35904974

Identifying phenotypic expansions for congenital diaphragmatic hernia plus (CDH+) using DECIPHER data.

Amy Hardcastle1, Aliska M Berry2, Ian M Campbell3, Xiaonan Zhao2,4, Pengfei Liu2,4, Amanda E Gerard2,5, Jill A Rosenfeld2, Saumya D Sisoudiya2, Andres Hernandez-Garcia2, Sara Loddo6, Silvia Di Tommaso6, Antonio Novelli6, Maria L Dentici7,8, Rossella Capolino7,8, Maria C Digilio7,8, Ludovico Graziani8,9, Cecilie F Rustad10, Katherine Neas11, Giovanni B Ferrero12, Alfredo Brusco13,14, Eleonora Di Gregorio14, Diana Wellesley15,16, Claire Beneteau17, Madeleine Joubert17, Kris Van Den Bogaert18, Anneleen Boogaerts18, Dominic J McMullan19, John Dean20, Maria G Giuffrida21, Laura Bernardini21, Vinod Varghese22, Nora L Shannon23, Rachel E Harrison23, Wayne W K Lam24, Shane McKee25, Peter D Turnpenny26, Trevor Cole27, Jenny Morton27, Jacqueline Eason23, Marilyn C Jones28, Rebecca Hall29, Michael Wright29, Karen Horridge30, Chad A Shaw2, Wendy K Chung31,32, Daryl A Scott2,5,33.   

Abstract

Congenital diaphragmatic hernia (CDH) can occur in isolation or in conjunction with other birth defects (CDH+). A molecular etiology can only be identified in a subset of CDH cases. This is due, in part, to an incomplete understanding of the genes that contribute to diaphragm development. Here, we used clinical and molecular data from 36 individuals with CDH+ who are cataloged in the DECIPHER database to identify genes that may play a role in diaphragm development and to discover new phenotypic expansions. Among this group, we identified individuals who carried putatively deleterious sequence or copy number variants affecting CREBBP, SMARCA4, UBA2, and USP9X. The role of these genes in diaphragm development was supported by their expression in the developing mouse diaphragm, their similarity to known CDH genes using data from a previously published and validated machine learning algorithm, and/or the presence of CDH in other individuals with their associated genetic disorders. Our results demonstrate how data from DECIPHER, and other public databases, can be used to identify new phenotypic expansions and suggest that CREBBP, SMARCA4, UBA2, and USP9X play a role in diaphragm development.
© 2022 Wiley Periodicals LLC.

Entities:  

Keywords:  CREBBP; DECIPHER database; SMARCA4; UBA2; USP9X; congenital diaphragmatic hernia

Mesh:

Year:  2022        PMID: 35904974      PMCID: PMC9474674          DOI: 10.1002/ajmg.a.62919

Source DB:  PubMed          Journal:  Am J Med Genet A        ISSN: 1552-4825            Impact factor:   2.578


  52 in total

1.  Mutations affecting components of the SWI/SNF complex cause Coffin-Siris syndrome.

Authors:  Yoshinori Tsurusaki; Nobuhiko Okamoto; Hirofumi Ohashi; Tomoki Kosho; Yoko Imai; Yumiko Hibi-Ko; Tadashi Kaname; Kenji Naritomi; Hiroshi Kawame; Keiko Wakui; Yoshimitsu Fukushima; Tomomi Homma; Mitsuhiro Kato; Yoko Hiraki; Takanori Yamagata; Shoji Yano; Seiji Mizuno; Satoru Sakazume; Takuma Ishii; Toshiro Nagai; Masaaki Shiina; Kazuhiro Ogata; Tohru Ohta; Norio Niikawa; Satoko Miyatake; Ippei Okada; Takeshi Mizuguchi; Hiroshi Doi; Hirotomo Saitsu; Noriko Miyake; Naomichi Matsumoto
Journal:  Nat Genet       Date:  2012-03-18       Impact factor: 38.330

2.  Prioritization of Candidate Genes for Congenital Diaphragmatic Hernia in a Critical Region on Chromosome 4p16 using a Machine-Learning Algorithm.

Authors:  Danielle A Callaway; Ian M Campbell; Samantha R Stover; Andres Hernandez-Garcia; Shalini N Jhangiani; Jaya Punetha; Ingrid S Paine; Jennifer E Posey; Donna Muzny; Kevin P Lally; James R Lupski; Chad A Shaw; Caraciolo J Fernandes; Daryl A Scott
Journal:  J Pediatr Genet       Date:  2018-05-30

3.  Cloning and expression analysis of a novel mouse gene with sequence similarity to the Drosophila fat facets gene.

Authors:  S A Wood; W S Pascoe; K Ru; T Yamada; J Hirchenhain; R Kemler; J S Mattick
Journal:  Mech Dev       Date:  1997-04       Impact factor: 1.882

Review 4.  Congenital posterolateral diaphragmatic hernia: associated malformations.

Authors:  D R Benjamin; S Juul; J R Siebert
Journal:  J Pediatr Surg       Date:  1988-10       Impact factor: 2.545

5.  Coffin-Siris Syndrome 4-Related Spectrum in a Young Woman Caused by a Heterozygous SMARCA4 Deletion Detected by High-Resolution aCGH.

Authors:  Anastasios Mitrakos; Leandros Lazaros; Amelia Pantou; Ariadni Mavrou; Emmanuel Kanavakis; Maria Tzetis
Journal:  Mol Syndromol       Date:  2020-06-13

6.  Genomic alterations that contribute to the development of isolated and non-isolated congenital diaphragmatic hernia.

Authors:  Margaret J Wat; Danielle Veenma; Jacob Hogue; Ashley M Holder; Zhiyin Yu; Jeanette J Wat; Neil Hanchard; Oleg A Shchelochkov; Caraciolo J Fernandes; Anthony Johnson; Kevin P Lally; Anne Slavotinek; Olivier Danhaive; Thomas Schaible; Sau Wai Cheung; Katherine A Rauen; Vijay S Tonk; Dick Tibboel; Annelies de Klein; Daryl A Scott
Journal:  J Med Genet       Date:  2011-05       Impact factor: 6.318

7.  De Novo Loss-of-Function Mutations in USP9X Cause a Female-Specific Recognizable Syndrome with Developmental Delay and Congenital Malformations.

Authors:  Margot R F Reijnders; Vasilios Zachariadis; Brooke Latour; Lachlan Jolly; Grazia M Mancini; Rolph Pfundt; Ka Man Wu; Conny M A van Ravenswaaij-Arts; Hermine E Veenstra-Knol; Britt-Marie M Anderlid; Stephen A Wood; Sau Wai Cheung; Angela Barnicoat; Frank Probst; Pilar Magoulas; Alice S Brooks; Helena Malmgren; Arja Harila-Saari; Carlo M Marcelis; Maaike Vreeburg; Emma Hobson; V Reid Sutton; Zornitza Stark; Julie Vogt; Nicola Cooper; Jiin Ying Lim; Sue Price; Angeline Hwei Meeng Lai; Deepti Domingo; Bruno Reversade; Jozef Gecz; Christian Gilissen; Han G Brunner; Usha Kini; Ronald Roepman; Ann Nordgren; Tjitske Kleefstra
Journal:  Am J Hum Genet       Date:  2016-01-28       Impact factor: 11.025

8.  SMARCA4 regulates gene expression and higher-order chromatin structure in proliferating mammary epithelial cells.

Authors:  A Rasim Barutcu; Bryan R Lajoie; Andrew J Fritz; Rachel P McCord; Jeffrey A Nickerson; Andre J van Wijnen; Jane B Lian; Janet L Stein; Job Dekker; Gary S Stein; Anthony N Imbalzano
Journal:  Genome Res       Date:  2016-07-19       Impact factor: 9.043

9.  The case for early use of rapid whole-genome sequencing in management of critically ill infants: late diagnosis of Coffin-Siris syndrome in an infant with left congenital diaphragmatic hernia, congenital heart disease, and recurrent infections.

Authors:  Nathaly M Sweeney; Shareef A Nahas; Shimul Chowdhury; Miguel Del Campo; Marilyn C Jones; David P Dimmock; Stephen F Kingsmore
Journal:  Cold Spring Harb Mol Case Stud       Date:  2018-06-01

10.  Nonsense variants of STAG2 result in distinct congenital anomalies.

Authors:  Hiromi Aoi; Ming Lei; Takeshi Mizuguchi; Nobuko Nishioka; Tomohide Goto; Sahoko Miyama; Toshifumi Suzuki; Kazuhiro Iwama; Yuri Uchiyama; Satomi Mitsuhashi; Atsuo Itakura; Satoru Takeda; Naomichi Matsumoto
Journal:  Hum Genome Var       Date:  2020-09-18
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