This hypomorphic allele was caused by the insertion of an intracisternal A particle into intron 4, which results in a decrease in transcript level to 25% of normal and an associated decrease in protein expression. (J:145608)
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count