A spontaneous mutant found to be allelic to Relnrl-Ord by complementation testing. The mutation was identified as a 24 kb deletion that comprises exons 13-20. Northern and western blot analysis confirmed the absence of expression in homozygotes. (J:79979)
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count