ArticleDisease models & mechanisms2013
Phenotypic overlap in the contribution of individual genes to CNV pathogenicity revealed by cross-species computational analysis of single-gene mutations in humans, mice and zebrafish.
Article in Disease models & mechanisms, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.
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Who cites it
32 citing papers in PubMed.
- Gene clustering drives the transcriptional coherence of disparate biological processes in eukaryotes.iScience · 2026Article
- Review
- Rare CNVs and phenome-wide profiling highlight brain structural divergence and phenotypical convergence.Nature human behaviour · 2023Article
- Prenatal phenotyping: A community effort to enhance the Human Phenotype Ontology.American journal of medical genetics. Part C, Seminars in medical genetics · 2022Article
- DeepSVP: integration of genotype and phenotype for structural variant prioritization using deep learning.Bioinformatics (Oxford, England) · 2022Article
- A cross-comparison of cognitive ability across 8 genomic disorders.Current opinion in genetics & development · 2021Review
- Genetics and epigenetics of autism spectrum disorder-current evidence in the field.Journal of applied genetics · 2019Review
- The Genetic Diagnosis of Neurodegenerative Diseases and Therapeutic Perspectives.Brain sciences · 2018Review
- Copy number gain of VCX, X-linked multi-copy gene, leads to cell proliferation and apoptosis during spermatogenesis.Oncotarget · 2016Article
- Computational evaluation of exome sequence data using human and model organism phenotypes improves diagnostic efficiency.Genetics in medicine : official journal of the American College of Medical Genetics · 2016Article
- Identification of genetic causes of congenital neurodevelopmental disorders using genome wide molecular technologies.Acta medica Lituanic · 2016Article
- Disease insights through cross-species phenotype comparisons.Mammalian genome : official journal of the International Mammalian Genome Society · 2015Review
- The clustering of functionally related genes contributes to CNV-mediated disease.Genome research · 2015Article
- Gene networks underlying convergent and pleiotropic phenotypes in a large and systematically-phenotyped cohort with heterogeneous developmental disorders.PLoS genetics · 2015Article
- Capturing domain knowledge from multiple sources: the rare bone disorders use case.Journal of biomedical semantics · 2015Article
- An ontology approach to comparative phenomics in plants.Plant methods · 2015Article
- Phenotype-driven strategies for exome prioritization of human Mendelian disease genes.Genome medicine · 2015Review
- Prioritizing Clinically Relevant Copy Number Variation from Genetic Interactions and Gene Function Data.PloS one · 2015Article
- Clinical interpretation of CNVs with cross-species phenotype data.Journal of medical genetics · 2014Article
- Deletions of chromosomal regulatory boundaries are associated with congenital disease.Genome biology · 2014Article
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13 authors.
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Abstract
Numerous disease syndromes are associated with regions of copy number variation (CNV) in the human genome and, in most cases, the pathogenicity of the CNV is thought to be related to altered dosage of the genes contained within the affected segment. However, establishing the contribution of individual genes to the overall pathogenicity of CNV syndromes is difficult and often relies on the identification of potential candidates through manual searches of the literature and online resources. We describe here the development of a computational framework to comprehensively search phenotypic information from model organisms and single-gene human hereditary disorders, and thus speed the interpretation of the complex phenotypes of CNV disorders. There are currently more than 5000 human genes about which nothing is known phenotypically but for which detailed phenotypic information for the mouse and/or zebrafish orthologs is available. Here, we present an ontology-based approach to identify similarities between human disease manifestations and the mutational phenotypes in characterized model organism genes; this approach can therefore be used even in cases where there is little or no information about the function of the human genes. We applied this algorithm to detect candidate genes for 27 recurrent CNV disorders and identified 802 gene-phenotype associations, approximately half of which involved genes that were previously reported to be associated with individual phenotypic features and half of which were novel candidates. A total of 431 associations were made solely on the basis of model organism phenotype data. Additionally, we observed a striking, statistically significant tendency for individual disease phenotypes to be associated with multiple genes located within a single CNV region, a phenomenon that we denote as pheno-clustering. Many of the clusters also display statistically significant similarities in protein function or vicinity within the protein-protein interaction network. Our results provide a basis for understanding previously un-interpretable genotype-phenotype correlations in pathogenic CNVs and for mobilizing the large amount of model organism phenotype data to provide insights into human genetic disorders.
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