This phenotypic mutation arose spontaneously at The Jackson Laboratory in 2000. Complementation testing with the dystonia Jackson mutation demonstrated this to be an allele at this locus.
Basic Information
B6;129S4-Gt(ROSA)26Sortm1Sor/J
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count