As this and most mutations at this locus are embryonic lethal in the homozygous state, complementation testing was not feasible. It is assumed to be allelic based on its phenotype and its map position.
Basic Information
B10.BR-H2k2 H2-T18a/SgSnJ
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count