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nstd161 (Nazaryan-Petersen et al. 2019)

Organism:
Human
Study Type:
Case-Set
Submitter:
Lusine Nazaryan-Petersen
Description:
Background: Moebius syndrome (MBS) is a congenital disorder primarily caused by unilateral or bilateral paralysis of the facial (cranial nerve VII) and abducens (cranial nerve VI) nerves. Both genetic defects and environmental toxic factors leading to abnormal brainstem development are proposed to be involved in the aetiology of MBS. Recently, mutations in PLXND1 and REV3L were confirmed to cause MBS. Although other candidate genes have been suspected, sequencing of MBS cohorts have not detected any causative mutations in them. Methods: Here, we applied next generation mate-pair sequencing to map the breakpoints of a complex chromosomal rearrangement (CCR) 46,XY,t(7;8;11;13) in a previously reported patient with MBS, and confirmed 39 out of 41 breakpoint-junctions by Sanger sequencing. Results: Molecular mapping revealed 41 clustered breakpoints, involving chromosomes 7, 8, 11 and 13, resulting in heavy intra- and interchromosomal rearrangements with typical hallmarks of chromothripsis. Among 12 truncated protein-coding genes, SEMA3A and SEMA3D are attractive candidates for the MBS features, as they encode class 3 semaphorins, where SEMA3A is known to bind to the MBS-associated PLXND1. Intriguingly, the CCR also truncated PIK3CG, which in silico interacts with a protein encoded by the other known MBS-gene REV3L, and with the SEMA3A/PLXND1 complex via the vascular endothelial growth factor FLT1. Conclusion: The simultaneous truncation of several interactors of the known MBS-genes by a single CCR suggests that the multiple breakpoints in germline chromothripsis may predispose to complex multigenic disorders. See Variant Summary counts for nstd161 in dbVar Variant Summary.
Publication(s):
Nazaryan-Petersen et al. 2019

Detailed Information: Download 4 Variant Regions, Download 41 Variant Calls, Download Both, FTP

Variant Summary

Assembly used for analysis:
Remapped: GRCh38.p12 (hg38)
Submitted: GRCh37 (hg19)

Sequence IDChrNumber of Variant RegionsNumber of Variant CallsPlacement typeLink to graphical display
NC_000007.14Chr7431RemappedNC_000007.14
NC_000008.11Chr8314RemappedNC_000008.11
NC_000011.10Chr1128RemappedNC_000011.10
NC_000013.11Chr1322RemappedNC_000013.11
Sequence IDChrNumber of Variant RegionsNumber of Variant CallsPlacement typeLink to graphical display
NC_000007.13Chr7431SubmittedNC_000007.13
NC_000008.10Chr8314SubmittedNC_000008.10
NC_000011.9Chr1128SubmittedNC_000011.9
NC_000013.10Chr1322SubmittedNC_000013.10

Variant Region remap statusVariant Call remap status
Sequence IDChrVariant Regions on sourcePerfectGoodPassFailMultVariant Calls on sourcePerfectGoodPassFailMult
NC_000007.13Chr740000100310000100
NC_000008.10Chr8300004014000040
NC_000011.9Chr1120000208000020
NC_000013.10Chr13200004200004

Samplesets

Number of Samplesets: 1

Size:
1
Organisms:
Homo sapiens
Sampleset Phenotype(s):
None reported
  • Download Samples as CSV file
  • Samples for sampleset 1
    Sample IDSubject ID Subject Phenotype
    D15358D15358Not reported

    Experimental Details

    Experiment IDTypeMethodAnalysisNumber of Variant Calls
    1DiscoverySequencingPaired-end mapping0
    2DiscoverySequencingSequence alignment0
    3DiscoveryMerging of experiments 1,2Merging of experiments 1,241

    Validations

    No validation data were submitted for this study.

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