In addition to the missense mutation, the deletion starts with the first base of the P114 codon and ends with the second base of the A123 codon. The 29 bases deleted are CCGTACGAGTGTCAGGTGCTTGTTTCGGC.
Amino acid replacement: R103C. In addition to the R103C mutation, there is also a 29bp deletion beginning in the P114 codon, which results in a frameshift.
29bp deletion which begins with the first base of codon P114. Causes a frameshift followed by 54 novel amino acid residues before early termination. The AmaR1 allele also contains a R103C missense mutation.
C6764146T
R103C | Ama-PA; R111C | Ama-PB; R103C | Ama-PC
R103C
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change. The AmaR1 allele also contains a 29bp deletion beginning in codon P114, which causes a frameshift.
Df(3R)ama/AmaR1 is an enhancer of abnormal neuroanatomy phenotype of Abl4/Abl1
AmaR1/Ama[+] is a non-enhancer of abnormal neuroanatomy phenotype of Abl4/Abl1
Df(3R)ama/AmaR1 is an enhancer of larval ventral nerve cord commissure phenotype of Abl4/Abl1
AmaR1/Ama[+] is a non-enhancer of larval ventral nerve cord commissure phenotype of Abl4/Abl1
104% of the expected number of Abl1 AmaR1/Abl4 pupae are observed, while 67% of the expected number of Abl1 AmaR1/Abl4 adults are observed. 4% of segments have commissure defects in the central nervous system of Abl1 AmaR1/Abl4 embryos. 23% of segments have commissure defects in the central nervous system of Abl1 AmaR1/Abl4 Df(3R)ama embryos.