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.
Legacy Phenotype Associated Images
malocclusion, head, abnormal snout morphology, asymmetric snout, HET, Male, WTSI
abnormal snout morphology, asymmetric snout, malocclusion, head, HET, Male, WTSI
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 Timeless by orthology or direct annotation.
The table below shows human diseases predicted to be associated to Timeless 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 Timeless.
There are 6 publications which use IMPC produced mice or data.
All available products are supplied via our member's centres or partnerships. When ordering a product from the IMPC you will be redirected to one of their websites or prompted to start an email.
|MGI Allele||Allele Type||Produced|
|Timelesstm1a(EUCOMM)Hmgu||KO first allele (reporter-tagged insertion with conditional potential)||Mice, Targeting vectors, ES Cells|
|Timelesstm1b(EUCOMM)Hmgu||Reporter-tagged deletion allele (with selection cassette)||Mice|
|Timelesstm1e(EUCOMM)Hmgu||Targeted, non-conditional allele||ES Cells|