The mission of the Mouse Genome Database (MGD) is to facilitate the use of mouse as a model system for understanding human biology and disease. To meet this objective in an era of rapidly emerging genome scale data sets for mouse and human, we serve three primary user communities: researchers who use mouse to investigate the genetic and molecular underpinnings of biology and disease processes, clinical researchers who use mouse models - to study. Specific human diseases and the computational biology/informatics community who leverage MGD's data integration capacity to develop algorithms and data analysis tools. To support the mouse genetics and genomics community we will (1) maintain the canonical, comprehensive catalog of mouse genes and other genome features, (2) annotate mouse genome features with their functional attributes using the Gene Ontology (GO), and (3) annotate mutant genotypes with Mammalian Phenotype (MP) Ontology terms, and curate those that are experimentally determined models of human genetic disease. Cross cutting all of these areas are the enforcement of official nomenclature for genome features, alleles, and mouse strains. To enhance MGD as a tool for the clinical research community we will expand our current coverage of Mendelian inherited human genetic disease models to include non- Mendelian diseases, such as metabolic syndromes, as well as susceptibility and modifier effects defined by QTL. To accomplish this, we will utilize current disease vocabularies and substantially contribute to emerging ontologies for human diseases and conditions. We will develop human-genome as well as mouse-genome views of disease loci and candidate genes. To enhance our support for the computational biology/informatics community we will further develop our Web Services API, Mouse BioMart, and Batch Query Tool for computational users. To meet the aims of this proposal we will maintain cost-effective hardware and software using industry best practices. To ensure the greatest impact of MGD in the broader scientific community we have a dedicated user support staff to provide technical assistance and training for our database users;we actively solicit community input, data submissions, and collaborations. We will continue to make all data in MGD freely available to all.

Public Health Relevance

Virtually all advances in human medicine rely on the use of animal models. Chief among these is the laboratory mouse. In this era of genome-scale, data-driven biomedical research, the Mouse Genome Database (MGD) plays a pivotal role in standardizing, integrating, and disseminating information about the laboratory mouse. MGD's goal is to facilitate use of the mouse as a model system for understanding human biology and disease and to enable development of new hypotheses for and new discoveries in human medicine.

Agency
National Institute of Health (NIH)
Institute
National Human Genome Research Institute (NHGRI)
Type
Biotechnology Resource Cooperative Agreements (U41)
Project #
5U41HG000330-25
Application #
8446526
Study Section
Special Emphasis Panel (ZHG1-HGR-M (O2))
Program Officer
Bonazzi, Vivien
Project Start
1997-07-01
Project End
2016-02-29
Budget Start
2013-03-01
Budget End
2014-02-28
Support Year
25
Fiscal Year
2013
Total Cost
$4,683,958
Indirect Cost
$2,274,126
Name
Jackson Laboratory
Department
Type
DUNS #
042140483
City
Bar Harbor
State
ME
Country
United States
Zip Code
04609
Eppig, Janan T; Blake, Judith A; Bult, Carol J et al. (2015) The Mouse Genome Database (MGD): facilitating mouse as a model for human biology and disease. Nucleic Acids Res 43:D726-36
Köhler, Sebastian; Doelken, Sandra C; Mungall, Christopher J et al. (2014) The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data. Nucleic Acids Res 42:D966-74
Park, Carissa A; Bello, Susan M; Smith, Cynthia L et al. (2013) The Vertebrate Trait Ontology: a controlled vocabulary for the annotation of trait data across species. J Biomed Semantics 4:13
Oetting, William S; Robinson, Peter N; Greenblatt, Marc S et al. (2013) Getting ready for the Human Phenome Project: the 2012 forum of the Human Variome Project. Hum Mutat 34:661-6