This TALEN-mediated mutation, generated in mice homozygous for the rd8 allele, is a 17 base pair intragenic deletion in exon 9 spanning nucleotides 3481-3497, which causes a frameshift with 7 amino acid substitutions before early termination. (J:265859)
Basic Information
B6.Cg-Crb1rd8 Jak3m1J/BocJ
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count