Possibly carries a deletion starting in H transcription unit.
lethal | recessive
visible | dominant
Intermediate H phenotype. H88d/TM6B shows extreme venation defects in L2 and the posterior crossvein is disrupted, with L5 complete.
Phenotypic series of H alleles, progressing from strongest (amorphic) to weakest mutant phenotype: HB79 = H81 >> H1 = H99 > Hbob > H94a > H88d > HB8 > H2 >= H3 > HA120.
Phenotypic series of H alleles, progressing from strongest (amorphic) to weakest mutant phenotype: HB79 = H81 >> H1 = H99 > Hbob > H94a > H88d > HB8 > H2 >= H3 > HA120.