Plekhg3 | pleckstrin homology domain containing, family G (with RhoGef domain) member 3
Physiological systems
18 / 24 physiological systems tested
1 Significantly impacted by the knock-out
Vision/eye
17 No significant impact
6 Not tested
Data collections
Gene metrics:1Significant phenotypes
0Associated diseases
Expression examined in:0Adult tissues
0Embryo tissues
Human diseases caused by Plekhg3 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
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