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| Status |
Public on Apr 04, 2018 |
| Title |
Tetra-Amelia with lung aplasia phenotype |
| Organism |
Homo sapiens |
| Experiment type |
Genome variation profiling by SNP array
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| Summary |
Clinical findings of this case has been reported previously by Sergio de Sousa (American Journal of Medical Genetics Part A 146A:2799–2803 (2008)). RSPO2 gene has been identified by our group (İstanbul, Turkey, 2014) as responsible gene for Tetra-Amelia with lung aplasia phenotype. To find causative pathogenic variations, sanger sequencing of fetal DNA was performed and did not reveal any variations. 300K SNP array was performed to analyse possible CNVs. A homozygous 154kb deletion on chr8 (deletion break points:108,809,266-108,963,256) covering intron 5 (partial), exon 6 and 3'UTR (partial) of RSPO2 gene was identified as the causative deletion.
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| Overall design |
Genomic DNA extracted from AF culture cells was scanned according to the array barcodes and Infinium HumanCytoSNP-12 v2.1 BeadChips datasheets (Illumina). Data was analysed with GenomeStudio Software (Illumina)
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| Contributor(s) |
Yucel EB, Altunoglu U, Kayserili H |
| Citation(s) |
29769720 |
| |
| Submission date |
Mar 13, 2018 |
| Last update date |
May 18, 2018 |
| Contact name |
Esra Yucel |
| E-mail(s) |
[email protected]
|
| Phone |
+905448504340
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| Organization name |
Koc University Hospital
|
| Department |
Diagnosis Centre For Genetic Disorders
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| Lab |
Molecular Genetics Lab
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| Street address |
Davutpasa Cd. No:4
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| City |
Istanbul |
| State/province |
Topkapı |
| ZIP/Postal code |
34010 |
| Country |
Turkey |
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| Platforms (1) |
| GPL13829 |
Illumina HumanCytoSNP-12 v2.1 BeadChip |
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| Samples (1) |
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| Relations |
| BioProject |
PRJNA438127 |
