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May 15, 2017
Additional lacZ knock in reporter data from the International Mouse Phenotyping Consortium (IMPC) have been imported into GXD. This set now comprises data for 1,112 targeted mutants, an increase of 468 mutants. It includes 39,510 images and their 44,551 annotated results, obtained from embryonic day 12.5 and postnatal adult specimens. These data are fully integrated into GXD, allowing them to be searched in context of all other gene expression data in GXD. The entire set can be viewed at reference J:228563.
May 1, 2017
This release includes embryonic phenotype data from the Deciphering the Mechanisms of Developmental Disorders (DMDD) consortium. All of the DMDD mouse lines are derived from IMPC EC cells or CRIPSR lines. For an example, see this Allele Detail page.
Included in this release are redesigns to the Mammalian Phenotype (MP), Gene Ontology (GO), and the Adult Mouse Anatomy Browsers.
MGI now includes C57BL/6J contig sequences for MGI markers that are located on contigs that are unlocalized and unplaced on the genome assembly. You can query by these contig sequences and return all associated markers. Details of a marker's location within a contig are provided in notes on Gene Detail pages in the Location & Maps section. As an example, see the Spry3 Gene Detail page.
March 13, 2017
Disease Ontology (DO) is incorporated into MGI.
The Disease Ontology (DO) is a community effort to provide standard terms for annotating phenotypic data. It is a hierarchical ontology, built on a Directed Acyclic Graph (DAG) structure, that integrates vocabularies from MeSH, ICD, NCI's thesaurus, SNOMED, UMLS, Orphanet, EFO and OMIM. Its hierarchical structure permits a range of detail from high-level, broadly descriptive terms to low-level, very specific terms. This range is useful for annotating mouse model data to the level of detail known and for searching for this information using either broad or specific terms as search criteria.
Existing MGI mouse human disease model annotations are now being translated to DO terms. You can use the MGI Disease Ontology Browser to navigate the ontology and see associated genes and mouse models. The genes and models tabs for higher level terms show all data for all of the more specific child terms. The MGI Quick Search field, Human - Mouse: Disease Connection, and other Query Forms' Phenotype / Disease field, support searches of the DO.
October 10, 2016
The MGI 6.06 release provides a new FTP server and other back end upgrades. The MGI FTP site address has changed from: ftp://ftp.informatics.jax.org/pub/
to: http://www.informatics.jax.org/downloads/.
August 1, 2016
The Human - Mouse: Disease Connection (HMDC) is designed to facilitate the identification of published and potential mouse models of human disease, discovery of candidate genes and investigation of phenotypic similarity between mouse models and human patients. The initial release integrated mouse mutation, phenotype and disease model data from MGI with human gene-to-disease relationships from Online Mendelian Inheritance in Man (OMIM). New in this release, human disease-to-phenotype relationships from the Human Phenotype Ontology (HPO) are integrated into HMDC.
This release also features a redesigned, streamlined, HMDC search form. You can easily search for combinations of human or mouse genome coordinates, multiple phenotype terms, disease terms, gene symbols, and accession identifiers (IDs).
July 13, 2016
Thank you for your support!
In just 2 weeks, over 10,000 signatures were collected in support of Model Organism Databases (MODs). The letter of support will be presented to NIH Director Francis Collins at The Allied Genetics Conference in Orlando this week. For more information, see the June 23, 2016 news item.
June 23, 2016
We wish to call your attention to a critical issue that has arisen for our community and that of other model organisms. The NIH institute, the National Human Genome Research Institute (NHGRI), that supports the Mouse Genome Database (MGD) and several other Model Organism Databases (MODs), and the Gene Ontology Consortium (GOC), is changing their funding approach. These changes are reported this week in Nature as well as previously in Science. NIH has put forth a plan where MGD and its equivalents for rat, C. elegans, yeast, zebrafish, and Drosophila would combine into a single 'uberMOD', with an upcoming 30% cut in funding. While integration will increase accessibility of the functional data that each community has collected over decades, the current plan with its reduced funding will have a severe impact on the ability of MGD to maintain mouse-specific datasets that many of us rely on daily.
Because of the concern about this plan and its broad impact on many thousands of researchers, leaders of model organism communities have come together to write a letter to NIH leadership that strongly supports the MODs and advocates for maintaining species-specific datasets with requisite funding. A bevy of prominent signatories, including Nobel laureates, heads of scientific societies, and National Academy members have already endorsed this initiative. We hope to gather thousands of additional signatures and present the letter to NIH Director Francis Collins at The Allied Genetics Conference in Orlando next month. The letter can be easily signed on a website, created by our partners at The Genetics Society of America (GSA), with your name and just two simple questions about your location and any NIH funding. These questions simply allow us to collate signatory numbers should NIH request a breakdown along these lines.
We urge you to add your name to the Statement of Support, as we aim to collect signatures from all MOD users who concur (for the question about NIH support, we can consider those who work in an NIH-funded lab to be NIH-supported). Finally, we encourage you to spread the word through your colleagues and via social media. We have every hope that a strong show of support, via an outpouring of signatures, will help shape the NHGRI plan to preserve the MOD features that are most important to our research enterprise.
May 30, 2016
LacZ knock in reporter data for 644 targeted mutants have been imported into GXD from the International Mouse Phenotyping Consortium (IMPC). This set includes 20,139 images and their 21,694 annotated results, obtained from embryonic day 12.5 and postnatal adult specimens. These data are fully integrated into GXD, allowing them to be searched in context of all other gene expression data in GXD. The entire set can be viewed at J:228563.
March 21, 2016
The MGI 6.03 release provides improvements to SNPs searches and batch Gene Expression data.
SNP Query enhancements:
  • The new MGI Mouse dbSNP Query is easier to use, provides vastly improved performance and updated data (dbSNP Build 142).
  • You can filter your results by dbSNP Function Classes and drag columns to reposition strains of interest.
Gene Expression Batch Search:
  • A Batch Search utility has been added, as a third tab, to the Gene Expression Data Query to facilitate searches for expression data using lists of gene symbols or IDs. You can search by either uploading a list of symbols or IDs from tab-delimited or comma-separated files or by copying and pasting a list into the text search box.
  • In addition, the genes field of the Standard Search now accepts comma-separated lists of gene symbols.
  • All Gene Expression Data searches return a tissue-by-gene matrix view as part of its multi-tabbed data summary; this view enables a comparison of expression patterns between genes. Data filters found on the summary pages can be used to further refine search results.
Links to Wikipedia human gene pages:
  • MGI Gene Detail pages now provide links to Wikipedia pages for human gene information. The MyGene.info project organizes these Wikipedia pages and MGI links to these pages only for genes that have a one-to-one mouse/human orthology relationship.
January 14, 2016
The MGI 6.02 release provides improvements to recombinase searches and Gene Ontology (GO) data.
Recombinase enhancements:
  • The MGI Recombinase search now permits querying for anatomical structures AND a driver.
  • The Driver field is now an autocomplete field.
  • Your recombinase search results can now be filtered by Driver, Inducer, Detected and Not Detected (anatomical system) columns.
  • In your search summary, if an inducer is required to activate recombinase activity, then the inducer is now indicated in the summary.
A tutorial for finding recombinase alleles in MGI is available at YouTube.
GO data enhancements:
  • GO tables contain a new Category column. Categories are from a subset of the Gene Ontologies (a "GO slim") and each category provides an overview of a section of the ontology.
  • A new Context column adds value to the GO classification term by detailing the conditions or refining the tissue used in the experiment.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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