IMPC Survey - Please provide your input!

The IMPC is at a funding crossroads and seeking community input.  Help shape the future of the IMPC by taking part in our short survey.

Fbxo42 | F-box protein 42

GeneMGI:1924992Genome BrowserSynonyms: 6720460I06Rik

Physiological systems

18 / 24 physiological systems tested

5 Significantly impacted by the knock-out

 Homeostasis/metabolism Hearing/vestibular/ear Hematopoietic system Cardiovascular system Mortality/aging

13 No significant impact

6 Not tested

Gene metrics:8Significant phenotypes
0Associated diseases
Expression examined in:0Adult tissues
0Embryo tissues

Phenotypes

  Loading...










* This parameter was manually assessed for significance.
Download data as:  

lacZ Expression

Associated images

Loading...

Human diseases caused by Fbxo42 mutations

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.






Download data as:  

Histopathology

Loading...

IMPC related publications

Loading...

Order Mouse and ES Cells

Loading...