Kcnj13 | potassium inwardly-rectifying channel, subfamily J, member 13
GeneMGI:3781032
Physiological systems
21 / 24 physiological systems tested
6 Significantly impacted by the knock-out
Embryo Growth/size/body region Digestive/alimentary Mortality/aging Cardiovascular system Craniofacial
15 No significant impact
3 Not tested
Data collections
Gene metrics:5Significant phenotypes
4Associated diseases
Expression examined in:50Adult tissues
0Embryo tissues
Human diseases caused by Kcnj13 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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