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From multiallele fish to nonstandard environments, how ZFIN assigns phenotypes, human disease models, and gene expression annotations to genes

Danio rerio is a model organism used to investigate vertebrate development. Manipulation of the zebrafish genome and resultant gene products by mutation or targeted knockdown has made the zebrafish a good system for investigating gene function, providing a resource to investigate genetic contributor...

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Autores principales: Bradford, Yvonne M, Van Slyke, Ceri E, Howe, Douglas G, Fashena, David, Frazer, Ken, Martin, Ryan, Paddock, Holly, Pich, Christian, Ramachandran, Sridhar, Ruzicka, Leyla, Singer, Amy, Taylor, Ryan, Tseng, Wei-Chia, Westerfield, Monte
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158835/
https://www.ncbi.nlm.nih.gov/pubmed/36864549
http://dx.doi.org/10.1093/genetics/iyad032
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author Bradford, Yvonne M
Van Slyke, Ceri E
Howe, Douglas G
Fashena, David
Frazer, Ken
Martin, Ryan
Paddock, Holly
Pich, Christian
Ramachandran, Sridhar
Ruzicka, Leyla
Singer, Amy
Taylor, Ryan
Tseng, Wei-Chia
Westerfield, Monte
author_facet Bradford, Yvonne M
Van Slyke, Ceri E
Howe, Douglas G
Fashena, David
Frazer, Ken
Martin, Ryan
Paddock, Holly
Pich, Christian
Ramachandran, Sridhar
Ruzicka, Leyla
Singer, Amy
Taylor, Ryan
Tseng, Wei-Chia
Westerfield, Monte
author_sort Bradford, Yvonne M
collection PubMed
description Danio rerio is a model organism used to investigate vertebrate development. Manipulation of the zebrafish genome and resultant gene products by mutation or targeted knockdown has made the zebrafish a good system for investigating gene function, providing a resource to investigate genetic contributors to phenotype and human disease. Phenotypic outcomes can be the result of gene mutation, targeted knockdown of gene products, manipulation of experimental conditions, or any combination thereof. Zebrafish have been used in various genetic and chemical screens to identify genetic and environmental contributors to phenotype and disease outcomes. The Zebrafish Information Network (ZFIN, zfin.org) is the central repository for genetic, genomic, and phenotypic data that result from research using D. rerio. Here we describe how ZFIN annotates phenotype, expression, and disease model data across various experimental designs, how we computationally determine wild-type gene expression, the phenotypic gene, and how these results allow us to propagate gene expression, phenotype, and disease model data to the correct gene, or gene related entity.
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spelling pubmed-101588352023-05-05 From multiallele fish to nonstandard environments, how ZFIN assigns phenotypes, human disease models, and gene expression annotations to genes Bradford, Yvonne M Van Slyke, Ceri E Howe, Douglas G Fashena, David Frazer, Ken Martin, Ryan Paddock, Holly Pich, Christian Ramachandran, Sridhar Ruzicka, Leyla Singer, Amy Taylor, Ryan Tseng, Wei-Chia Westerfield, Monte Genetics Knowledgebase and Database Resources Danio rerio is a model organism used to investigate vertebrate development. Manipulation of the zebrafish genome and resultant gene products by mutation or targeted knockdown has made the zebrafish a good system for investigating gene function, providing a resource to investigate genetic contributors to phenotype and human disease. Phenotypic outcomes can be the result of gene mutation, targeted knockdown of gene products, manipulation of experimental conditions, or any combination thereof. Zebrafish have been used in various genetic and chemical screens to identify genetic and environmental contributors to phenotype and disease outcomes. The Zebrafish Information Network (ZFIN, zfin.org) is the central repository for genetic, genomic, and phenotypic data that result from research using D. rerio. Here we describe how ZFIN annotates phenotype, expression, and disease model data across various experimental designs, how we computationally determine wild-type gene expression, the phenotypic gene, and how these results allow us to propagate gene expression, phenotype, and disease model data to the correct gene, or gene related entity. Oxford University Press 2023-03-02 /pmc/articles/PMC10158835/ /pubmed/36864549 http://dx.doi.org/10.1093/genetics/iyad032 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Genetics Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Knowledgebase and Database Resources
Bradford, Yvonne M
Van Slyke, Ceri E
Howe, Douglas G
Fashena, David
Frazer, Ken
Martin, Ryan
Paddock, Holly
Pich, Christian
Ramachandran, Sridhar
Ruzicka, Leyla
Singer, Amy
Taylor, Ryan
Tseng, Wei-Chia
Westerfield, Monte
From multiallele fish to nonstandard environments, how ZFIN assigns phenotypes, human disease models, and gene expression annotations to genes
title From multiallele fish to nonstandard environments, how ZFIN assigns phenotypes, human disease models, and gene expression annotations to genes
title_full From multiallele fish to nonstandard environments, how ZFIN assigns phenotypes, human disease models, and gene expression annotations to genes
title_fullStr From multiallele fish to nonstandard environments, how ZFIN assigns phenotypes, human disease models, and gene expression annotations to genes
title_full_unstemmed From multiallele fish to nonstandard environments, how ZFIN assigns phenotypes, human disease models, and gene expression annotations to genes
title_short From multiallele fish to nonstandard environments, how ZFIN assigns phenotypes, human disease models, and gene expression annotations to genes
title_sort from multiallele fish to nonstandard environments, how zfin assigns phenotypes, human disease models, and gene expression annotations to genes
topic Knowledgebase and Database Resources
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10158835/
https://www.ncbi.nlm.nih.gov/pubmed/36864549
http://dx.doi.org/10.1093/genetics/iyad032
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