Spin2c | spindlin family, member 2C
Physiological systems
17 / 24 physiological systems tested
17 No significant impact
7 Not tested
Data collections
Gene metrics:0Significant phenotypes
0Associated diseases
Expression examined in:96Adult tissues
50Embryo tissues
Human diseases caused by Spin2c 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.
External links
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