Gene: Ppp1r21 MGI:1921075
Log in to followHuman diseases caused by Ppp1r21 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.
The table below shows human diseases associated to Ppp1r21 by orthology or direct annotation.
Disease | Similarity of phenotypes |
Matching phenotypes | Source |
---|---|---|---|
Neurodevelopmental Disorder With Hypotonia, Facial Dysmorphism, And Brain Abnormalities | OMIM:619383 |
The table below shows human diseases predicted to be associated to Ppp1r21 by phenotypic similarity.
Disease | Similarity of phenotypes |
Matching phenotypes | Source |
---|---|---|---|
Neurodevelopmental Disorder With Hypotonia, Facial Dysmorphism, And Brain Abnormalities | OMIM:619383 |
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