exMGH2 is reported as an 8bp deletion that causes a frameshift after amino acid 957 and truncates the protein 34 amino acids downstream. The deleted region may be shifted one base 3' relative to the direction of ex transcription.
Eight base pair deletion mutation that shifts the ex reading frame after amino acid 957, and results in truncation of the protein 34 amino acids after the frame shift.
hyperplasia | larval stage (with exMGH1)
eye | somatic clone
eye-antennal disc (with exMGH1)
photoreceptor cell (with exMGH1)
wing disc (with exMGH1)
exMGH2 mosaic clones in the eye display a strong over proliferation phenotype.