Registered for phenotyping at IMPC
Phenotyping is planned for a knockout strain of this gene but data is not currently available.
Gene Summary
IMPC Data Collections
- No Body Weight Data
- No Embryo Imaging Data
- No Viability Data
Phenotyping is planned for a knockout strain of this gene but data is not currently available.
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.
The table below shows human diseases predicted to be associated to Kcnj15 by phenotypic similarity.
Disease | Similarity of phenotypes |
Matching phenotypes | Source |
---|---|---|---|
Posterior Column Ataxia | Impaired vibratory sensation, Ataxia, Impaired proprioception | OMIM:176250 | |
Spinocerebellar Ataxia Type 23 | Impaired distal vibration sensation, Impaired proprioception, Limb ataxia, Dysmetria, Gait ataxia... | ORPHA:101108 | |
Chorea, Benign Familial | Chorea | OMIM:215450 |
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MGI Allele | Allele Type | Produced |
---|---|---|
Kcnj15em1(IMPC)Bay | Exon Deletion | Mice |
Kcnj15tm1e(EUCOMM)Wtsi | Targeted, non-conditional allele | ES Cells |
Kcnj15tm1a(EUCOMM)Wtsi | KO first allele (reporter-tagged insertion with conditional potential) | Targeting vectors, ES Cells |
Kcnj15tm1(KOMP)Vlcg | Reporter-tagged deletion allele (with selection cassette) | ES Cells |
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