Gene Summary
IMPC Data Collections
- Body Weight Measurements
- No Embryo Imaging Data
- Viability Data
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 associated to Lipt2 by orthology or direct annotation.
Disease | Similarity of phenotypes |
Matching phenotypes | Source |
---|---|---|---|
Encephalopathy, Neonatal Severe, With Lactic Acidosis And Brain Abnormalities | OMIM:617668 |
The table below shows human diseases predicted to be associated to Lipt2 by phenotypic similarity.
Disease | Similarity of phenotypes |
Matching phenotypes | Source |
---|---|---|---|
Encephalopathy, Neonatal Severe, With Lactic Acidosis And Brain Abnormalities | OMIM:617668 |
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