Not currently registered for phenotyping at IMPC
Phenotyping is currently not planned for a knockout strain of this gene.
Gene Summary
IMPC Data Collections
- No Body Weight Data
- No Embryo Imaging Data
- No Viability Data
Phenotyping is currently not planned for a knockout strain of this gene.
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 Piga by orthology or direct annotation.
Disease | Similarity of phenotypes |
Matching phenotypes | Source |
---|---|---|---|
Paroxysmal Nocturnal Hemoglobinuria 1 | OMIM:300818 | ||
Infantile Spasms Syndrome | ORPHA:3451 | ||
Neurodevelopmental Disorder With Epilepsy And Hemochromatosis | OMIM:301072 | ||
Malignant Migrating Focal Seizures Of Infancy | ORPHA:293181 | ||
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 | OMIM:300868 | ||
Paroxysmal Nocturnal Hemoglobinuria | ORPHA:447 |
The table below shows human diseases predicted to be associated to Piga by phenotypic similarity.
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