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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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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. |
format | Online Article Text |
id | pubmed-10158835 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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