Skip to main content
. 2007 Nov 23;9(1):76–83. doi: 10.1038/sj.embor.7401122

Table 1.

groucho alleles for which molecular data were obtainable

Type of lesion Allele Base change* RNA/protein changes
Nonsense
  MBB G4624A W550stop
  MB6 C2315T R190stop
  MB11 C4769T Q599stop
  MB25 C4361T Q463stop, as MB27
  MB27 C4361T Q463stop, as MB25
  MB34 G4749A W592stop
  MB42 G4716A W581stop
Frameshift
  MB13 G2485A Splice junction mutated, frameshift from residue 225 as intronic sequences transcribed, as MB37
  MB15 G138A Ectopic splice acceptor site in intron, frameshift from residue 13, as MB36
  MB18 G266A Splice junction mutated, frameshift from residue 45 as intronic sequences transcribed
  MB33 Δ3782–3813 31 bp deletion; frameshift from residue 103
  MB36 G138A as MB15
  MB37 G2485A as MB13
Other
  MB5 T189C P19S, Δ19–27
    C190T See Fig 2B for sequence
    Δ191–214  
  MB12 G3A Initiator ATG → ATA
Missense
  MBD A4613T I547F
  MB19 G4683A C570Y
  MB21 G4422A R483H, as MB41
  MB30 A4977C H646P
  MB31 C5176T L692F
  MB35 G4326A G451D
  MB41 G4422A R483H, as MB21
*Bases numbered from the start of translation, corresponding to 3R:21869066 Drosophila melanogaster genome Release 5.1.
For characterization of missense alleles, refer to Jennings et al (2006).