Nucleotide substitution: C1373T.
Amino acid replacement: Q408term.
Mutation creates a stop codon that interrupts the open reading frame of the three MED1 isoforms. (The location of the point mutation is a revision of data reported in FBrf0241861).
C21633009T
Q408term | MED1-PA; Q408term | MED1-PB; Q408term | MED1-PC
Q408term
MED1O2 homozygous mutant clones in the dorsal part of the wing disc (ap-Gal4>UAS-Flp) are often restricted to a single cell, while larger twin-spot wild-type clones are common. Larger mutant clones are retrieved when in a Minute background.
Induction of MED1O2 mutant clones in a Minute background leads to mosaic adults displaying thoracic clefts and loss of dorsocentral mechanosensory macrochaetae, as compared to wild-type controls.