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 Mir29a by phenotypic similarity.
Disease | Similarity of phenotypes |
Matching phenotypes | Source |
---|---|---|---|
Anterior Cutaneous Nerve Entrapment Syndrome | Allodynia, Nausea | ORPHA:51890 | |
Complex Regional Pain Syndrome | Allodynia | ORPHA:83452 | |
Trigeminal Neuralgia | Allodynia | ORPHA:221091 | |
Mitochondrial Dna Depletion Syndrome 1 (Mngie Type) | Gastroparesis, Diarrhea, Constipation, Vomiting, Dysphagia, Intermittent diarrhea, Allodynia | OMIM:603041 | |
Neurotrophic Keratopathy | Allodynia | ORPHA:137596 | |
Benign Schwannoma | Allodynia | ORPHA:252164 |
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MGI Allele | Allele Type | Produced |
---|---|---|
Mir29atm1(mirKO)Wtsi | Reporter-tagged deletion allele (with selection cassette) | Targeting vectors, ES Cells |
Mir29aem1(IMPC)Mhzh | Deletion | Mice |
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