Exons 2-6 were flanked by loxP sites, creating a conditional ready allele. Deletion of these exons would cause a frameshift and premature termination of the reading frame. (J:238730)
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count