Used to study clubfoot and neurogenic-type arthrogryposis multiplex congenita-2.
MGI Description
PHENOTYPE: Mice homozygous for a spontaneous allele display a club foot and ankle joint immobility at birth, show peroneal muscular atrophy in the hind limbs due to absence of the common peroneal nerve branch, and develop an unusual gait due to a dropped foot in adulthood. [provided by MGI curators]