The IMPC applies a panel of phenotyping screens to characterise single-gene knockout mice by comparison to wild types. Click on the different tabs to visualise significant phenotypes identified by the IMPC, as well as all data that was measured.
Images submitted by IMPC centres for a selection of procedures. Each set of images is available to view in our image comparator.
The analysis uses data from IMPC, along with published data on other mouse mutants, in comparison to human disease reports in OMIM, Orphanet, and DECIPHER.
Phenotype comparisons summarize the similarity of mouse phenotypes with human disease phenotypes.
The table below shows human diseases associated to Exosc1 by orthology or direct annotation.
The table below shows human diseases predicted to be associated to Exosc1 by phenotypic similarity.
The table below lists publications which used either products generated by the IMPC or data produced by the phenotyping efforts of the IMPC. These publications have also been associated to Exosc1.
There are 2 publications which use IMPC produced mice or data.
|Title||Journal||IMPC Allele||PubMed ID|
|EXOSC10/Rrp6 is essential for the eight-cell embryo/morula transition.||Developmental biology (December 2021)||Exosc10tm1a(KOMP)Wtsi||34965385|
|EXOSC10/Rrp6 is post-translationally regulated in male germ cells and controls the onset of spermatogenesis.||Scientific reports (November 2017)||Exosc10tm1c(KOMP)Wtsi Exosc10tm1a(KOMP)Wtsi||PMC5678167|
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|MGI Allele||Allele Type||Produced|
|Exosc1tm1e(EUCOMM)Hmgu||Targeted, non-conditional allele||ES Cells|
|Exosc1tm1a(EUCOMM)Hmgu||KO first allele (reporter-tagged insertion with conditional potential)||Targeting vectors, ES Cells|