Wipi2 | WD repeat domain, phosphoinositide interacting 2

GeneMGI:1923831Synonyms: 1110018O08Rik, 2510001I10Rik

Physiological systems

16 / 24 physiological systems tested

2 Significantly impacted by the knock-out

 Vision/eye Mortality/aging

14 No significant impact

8 Not tested

Gene metrics:2Significant phenotypes
1Associated diseases
Expression examined in:0Adult tissues
0Embryo tissues

Phenotypes

preweaning lethality, complete penetrance2 supporting datasetsWipi2em1(IMPC)BayhomozygoteEarly adultN/A * 
increased total retina thickness1 supporting datasetWipi2em1(IMPC)BayheterozygoteEarly adult2.76x10-5 
* Does not have a P-value assigned because it was manually marked as significant.
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* This parameter was manually assessed for significance.
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lacZ Expression

Human diseases caused by Wipi2 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.






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Histopathology

IMPC related publications

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Order Mouse and ES Cells

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Wipi2em1(IMPC)BayExon Deletionmouse
Wipi2tm1a(EUCOMM)HmguKO first allele (reporter-tagged insertion with conditional potential)targeting vector
ES Cell
Wipi2tm1e(EUCOMM)HmguTargeted, non-conditional alleleES Cell

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