ZFIN: The Zebrafish Model Organism Database
ZFIN:斑马鱼模式生物数据库
基本信息
- 批准号:10369589
- 负责人:
- 金额:$ 211.2万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2003
- 资助国家:美国
- 起止时间:2003-07-11 至 2026-02-28
- 项目状态:未结题
- 来源:
- 关键词:AdoptedAffectAnimal ModelAntisense OligonucleotidesBase SequenceBehaviorBiologicalBiomedical ResearchCodeCommunitiesComputer softwareDataData ScienceData SetDatabasesDevelopmentDiseaseElementsEvolutionFAIR principlesGene ExpressionGenerationsGenesGeneticGenetic ModelsGenomeGenomicsGoalsGuidelinesHumanHuman BiologyHuman GenomeIndividualIndustry StandardInformation NetworksInfrastructureInternationalLaboratoriesLinkMetadataModelingMutateMutationNomenclatureOrganismOrganogenesisOrthologous GeneOther GeneticsPatternPhenotypePhysiologicalPhysiologyPlayProcessProteinsPublicationsReadabilityRecoveryResearchResearch ActivityResearch PersonnelResourcesRoleSiteSocietiesSoftware ToolsStrategic PlanningStructureSurveysTechniquesTechnologyTrainingTransgenic OrganismsUnited States National Institutes of HealthUpdateVertebrate BiologyVertebratesVisualizationWorkZebrafishdata accessdata curationdata exchangedata managementdata resourcegene functiongenetic analysisgenome analysisgenome editinggenome resourcehuman diseasehuman modelimprovedinsightknock-downknockout genemeetingsmodel organisms databasesoutreachpublic databasereference genomerepositorysoftware systemssymposiumtime usetooluser centered designweb sitewiki
项目摘要
Discovering the functions of the tens of thousands of genes in the human genome is a required step for
understanding human biology and disease. Genetic model organisms, including zebrafish, play a critical role in
this discovery process, because genetic analysis can connect gene sequence and function. Model organism
databases, like ZFIN, provide tools required to make this connection.
The zebrafish has emerged as a premier organism to study vertebrate biology. Powerful techniques allow
rapid efficient generation and recovery of mutations affecting genes that orchestrate developmental patterning,
organogenesis, physiology, and behavior. It is easy to study gene function by generating transgenic zebrafish,
by knocking down gene function with morpholino antisense oligonucleotides, or by altering gene function by
genome editing. The genome has been sequenced and about 50% of the protein coding genes have been
mutated by targeted gene knockout technology. Large-scale projects are underway or planned that will
produce functional data about almost all the genes and sequence-based functional elements in the genome.
Multiple mutations and gene knockdowns can be combined in the same individual to study gene modifiers and
other genetic interactions. The functions of most of these genes are conserved among vertebrate groups.
Thus, analysis of zebrafish mutations provides insights into gene functions in other vertebrates, including
humans.
The long term goals for ZFIN are a) to be the community database resource for the laboratory use of
zebrafish, b) to develop and support integrated zebrafish genetic, genomic, developmental, and physiological
information, c) to maintain the definitive reference data sets of zebrafish research information, d) to link this
information extensively to corresponding data in other model organism and human databases, e) to facilitate
the use of zebrafish as a model for human biology, and f) to help serve the broad needs of the biomedical
research community.
This project will continue and expand curation of zebrafish research data, develop expanded support for
zebrafish models of human disease, expand and integrate links to other databases, and maintain and update
the zebrafish reference genome. This work will provide a powerful means for researchers to associate gene
sequence and function, thus facilitating studies of human gene function and disease as well as cross-species
analyses of genome organization and evolution.
Discovering the functions of the tens of thousands of genes in the human genome is a required step for
understanding human biology and disease. Genetic model organisms, including zebrafish, play a critical role in
this discovery process, because genetic analysis can connect gene sequence and function. Model organism
databases, like ZFIN, provide tools required to make this connection.
The zebrafish has emerged as a premier organism to study vertebrate biology. Powerful techniques allow
rapid efficient generation and recovery of mutations affecting genes that orchestrate developmental patterning,
organogenesis, physiology, and behavior. It is easy to study gene function by generating transgenic zebrafish,
by knocking down gene function with morpholino antisense oligonucleotides, or by altering gene function by
genome editing. The genome has been sequenced and about 50% of the protein coding genes have been
mutated by targeted gene knockout technology. Large-scale projects are underway or planned that will
produce functional data about almost all the genes and sequence-based functional elements in the genome.
Multiple mutations and gene knockdowns can be combined in the same individual to study gene modifiers and
other genetic interactions. The functions of most of these genes are conserved among vertebrate groups.
Thus, analysis of zebrafish mutations provides insights into gene functions in other vertebrates, including
humans.
The long term goals for ZFIN are a) to be the community database resource for the laboratory use of
zebrafish, b) to develop and support integrated zebrafish genetic, genomic, developmental, and physiological
information, c) to maintain the definitive reference data sets of zebrafish research information, d) to link this
information extensively to corresponding data in other model organism and human databases, e) to facilitate
the use of zebrafish as a model for human biology, and f) to help serve the broad needs of the biomedical
research community.
This project will continue and expand curation of zebrafish research data, develop expanded support for
zebrafish models of human disease, expand and integrate links to other databases, and maintain and update
the zebrafish reference genome. This work will provide a powerful means for researchers to associate gene
sequence and function, thus facilitating studies of human gene function and disease as well as cross-species
analyses of genome organization and evolution.
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Monte Westerfield其他文献
Monte Westerfield的其他文献
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{{ truncateString('Monte Westerfield', 18)}}的其他基金
Genetic and functional analysis of YPEL3 and its link to disease
YPEL3 的遗传和功能分析及其与疾病的联系
- 批准号:
9070011 - 财政年份:2015
- 资助金额:
$ 211.2万 - 项目类别:
The functions of PDZ domain scaffold proteins in Usher syndrome
PDZ结构域支架蛋白在Usher综合征中的功能
- 批准号:
8099700 - 财政年份:2010
- 资助金额:
$ 211.2万 - 项目类别:
The functions of PDZ domain scaffold proteins in Usher syndrome
PDZ结构域支架蛋白在Usher综合征中的功能
- 批准号:
8471097 - 财政年份:2010
- 资助金额:
$ 211.2万 - 项目类别:
The functions of PDZ domain scaffold proteins in Usher syndrome
PDZ结构域支架蛋白在Usher综合征中的功能
- 批准号:
8662744 - 财政年份:2010
- 资助金额:
$ 211.2万 - 项目类别:
The functions of PDZ domain scaffold proteins in Usher syndrome
PDZ结构域支架蛋白在Usher综合征中的功能
- 批准号:
8301725 - 财政年份:2010
- 资助金额:
$ 211.2万 - 项目类别:
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