Amino acid replacement: Y829H.
Nucleotide substitution: T?C. Amino acid replacement: Y?H. Mutation is in exon 12, in the region that binds the regulatory light chain.
T16780751C
T?C
Y829H | Mhc-PA; Y829H | Mhc-PB; Y829H | Mhc-PC; Y829H | Mhc-PD; Y829H | Mhc-PE; Y829H | Mhc-PF; Y829H | Mhc-PG; Y829H | Mhc-PH; Y829H | Mhc-PI; Y829H | Mhc-PK; Y829H | Mhc-PL; Y829H | Mhc-PM; Y829H | Mhc-PN; Y829H | Mhc-PO; Y829H | Mhc-PP; Y829H | Mhc-PQ; Y829H | Mhc-PR; Y829H | Mhc-PS; Y829H | Mhc-PT; Y829H | Mhc-PU; Y829H | Mhc-PV
Y829H
Heterozygotes have an indented thorax, upheld wings, and are flightless.
Heterozygotes display indented thorax and erect wings. Judged to be antimorphic since not rescued by addition of Dp(2;3)osp3. Mhc8 interaction in double heterozygotes with other flightless mutants observed by Homyk and Emerson (1988). Heterozygous viability severely reduced in combination with either heterozygous or hemizygous wupAhdp-2, upint-3 and up101; lethal in upx/Y males. No interaction with the following: wupAhdp-3, wupAhdp-4, wupAhdp-5, wupAhdp-101, fliH1, up2 or up3.
The dominant phenotype is not rescued by Dp(2;3)osp3, which carries a duplication of the Mhc gene, suggesting this allele is an antimorph.
Mogami.