Nucleotide substitution: C569T. Nucleotide substitution: A570G. In addition to the two missense mutations, there is a single base pair deletion at nucleotide 572. These changes are predicted to cause a frameshift at amino acid 133 and the early truncation of the protein at residue 158.
Nucleotide substitution: C578T. Nucleotide substitution: A579G. 1 bp deletion of C581. Amino acid replacement: N133E. Frameshift causes 24 novel amino acids before a stop codon.
N133E|CG3511-PA
Deletion of a single C residue leads to a frameshift and truncation of the CDS after 24 novel amino acids. Two missense mutations are also observed in CG35111.
C24572408T
C569T
T132T | CG3511-PA; T132T | CG3511-PB
T133T
One of two missense mutations observed in CG35111. In addition, a single base is deleted leading to a frameshift.
A24572409G
A570G
N133D | CG3511-PA; N133D | CG3511-PB
N133E
One of two missense mutations observed in CG35111. In addition, a single base is deleted in same codon leading to a frameshift.
Homozygous clones in the eye induced in an Rbf+ background are viable. Homozygous larvae have an enlarged body phenotype compared to their heterozygous siblings. These "large larvae" wander for an extended period before death, although rare escapers can progress to giant pupae that fail to eclose as adults.
CG35111, RbfSLS-15 has cell lethal | somatic clone phenotype
Selected as: a mutation that results in synthetic cell lethality in clones in the eye in a RbfSLS-15 background.