This heritable allele is a derivative of Fgfr1tm3Cxd in which exons 8-14 and flanking sequences were deleted by Cre mediated recombination. (J:75137)
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count