Last Chance! IMPC survey closing in August!

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.

Kif1b | kinesin family member 1B

GeneMGI:108426Genome BrowserSynonyms: D4Mil1e, Kif1b alpha, +5 more

Physiological systems

19 / 24 physiological systems tested

10 Significantly impacted by the knock-out

 Homeostasis/metabolism Embryo Growth/size/body region Limbs/digits/tail Hearing/vestibular/ear Hematopoietic system Behavior/neurological Cardiovascular system Mortality/aging Craniofacial

9 No significant impact

5 Not tested

Gene metrics:17Significant phenotypes
4Associated diseases
Expression examined in:48Adult tissues
53Embryo tissues

Phenotypes

  Loading...










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

lacZ Expression

Associated images

Loading...

Human diseases caused by Kif1b 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...

The IMPC Newsletter

Get highlights of the most important data releases, news and events, delivered straight to your email inbox

Subscribe to newsletter