Wdr49 | WD repeat domain 49
Physiological systems
21 / 24 physiological systems tested
2 Significantly impacted by the knock-out
Integument Cardiovascular system
19 No significant impact
3 Not tested
Data collections
Gene metrics:2Significant phenotypes
0Associated diseases
Expression examined in:0Adult tissues
0Embryo tissues
abnormal skin morphology | 1 supporting dataset | Wdr49em1(IMPC)Ccpcz | homozygote | Early adult | N/A * | ||
abnormal heart morphology | 1 supporting dataset | Wdr49em1(IMPC)Ccpcz | homozygote | Early adult | N/A * |
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Human diseases caused by Wdr49 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.
External links
No external links available for Wdr49.
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Wdr49em1(IMPC)Ccpcz | Exon Deletion | | mouse |