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ConVarT: a search engine for matching human genetic variants with variants from non-human species

The availability of genetic variants, together with phenotypic annotations from model organisms, facilitates comparing these variants with equivalent variants in humans. However, existing databases and search tools do not make it easy to scan for equivalent variants, namely ‘matching variants’ (Matc...

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Detalles Bibliográficos
Autores principales: Pir, Mustafa S, Bilgin, Halil I, Sayici, Ahmet, Coşkun, Fatih, Torun, Furkan M, Zhao, Pei, Kang, Yahong, Cevik, Sebiha, Kaplan, Oktay I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8728286/
https://www.ncbi.nlm.nih.gov/pubmed/34718716
http://dx.doi.org/10.1093/nar/gkab939
Descripción
Sumario:The availability of genetic variants, together with phenotypic annotations from model organisms, facilitates comparing these variants with equivalent variants in humans. However, existing databases and search tools do not make it easy to scan for equivalent variants, namely ‘matching variants’ (MatchVars) between humans and other organisms. Therefore, we developed an integrated search engine called ConVarT (http://www.convart.org/) for matching variants between humans, mice, and Caenorhabditis elegans. ConVarT incorporates annotations (including phenotypic and pathogenic) into variants, and these previously unexploited phenotypic MatchVars from mice and C. elegans can give clues about the functional consequence of human genetic variants. Our analysis shows that many phenotypic variants in different genes from mice and C. elegans, so far, have no counterparts in humans, and thus, can be useful resources when evaluating a relationship between a new human mutation and a disease.