TMEM231 Gene Conversion Associated with Joubert and Meckel–Gruber Syndromes in the Same Family

NISC Comparative Sequencing Program

Research output: Contribution to journalArticlepeer-review

Abstract

Joubert and Meckel–Gruber syndromes (JS and MGS) are ciliopathies with overlapping features. JS patients manifest the “molar tooth sign” on brain imaging and variable eye, kidney, and liver disease. MGS presents with polycystic kidneys, occipital encephalocele, and polydactyly; it is typically perinatally fatal. Both syndromes are genetically heterogeneous; some genes cause either syndrome. Here, we report two brothers married to unrelated women. The first brother had three daughters with JS and a son with polycystic kidneys who died at birth. The second brother's wife had a fetal demise due to MGS. Whole exome sequencing identified TMEM231 NM_001077416.2: c.784G>A; p.(Asp262Asn) in all children and the wife of the first brother; the second brother's wife had a c.406T>G;p.(Trp136Gly) change. In-depth analysis uncovered a rare gene conversion event in TMEM231, leading to loss of exon 4, in all the affected children of first brother. We believe that the combination of this gene conversion with different missense mutations led to a spectrum of phenotypes that span JS and MGS.

Original languageEnglish (US)
Pages (from-to)1144-1148
Number of pages5
JournalHuman mutation
Volume37
Issue number11
DOIs
StatePublished - Nov 1 2016
Externally publishedYes

Keywords

  • TMEM231
  • cilia
  • gene conversion
  • translocation
  • whole exome sequencing

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Fingerprint Dive into the research topics of 'TMEM231 Gene Conversion Associated with Joubert and Meckel–Gruber Syndromes in the Same Family'. Together they form a unique fingerprint.

Cite this