This mutation was generated by cre recombinase excision of loxP flanked exons 3 and 4 leaving a single loxP site. RNA splicing of exon 2 to exon 5 is predicted to result in a reading-frame shift. (J:215741)
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count