ENU mutagenesis induced a G to A point mutation at position 464 on cDNA (ENSMUST00000114908) in exon 4 and results in the amino acid substitution of Arginine to STOP at position 56 (R56X). (J:104190)
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count