Sprr1a | small proline-rich protein 1A
Physiological systems
2 Significantly impacted by the knock-out
16 No significant impact
6 Not tested
Data collections
Human diseases caused by Sprr1a 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.