Phenotype: abnormal rostral-caudal axis patterning

anomaly in the development or formation of the axis that runs from the head to the tail of the body
abnormal head-tail axis patterning,  abnormal rostro-caudal axis patterning
of tested genes
significant genes
tested genes

IMPC Gene variants with abnormal rostral-caudal axis patterning

Phenotype associations to genes and alleles will be available once data has completed quality control.

 The way we measure

 Phenotype associations stats

0.00% of tested genes with null mutations on a B6N genetic background have a phenotype association to abnormal rostral-caudal axis patterning (0/235)

0.00% females (0/1) 0.00% males (0/1)

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