Amino acid replacement: E?term.
Affects an exon common to both Xrp1 isoforms of the protein and is predicted to truncate the long form after Thr367 and the short form after Thr105, before an AT-hook motif and bZip domain that occur near the C-termini of both isoforms.
Nucleotide substitution: G?T.
A G to T transition in the second exon of the Xrp1 gene (position 3R:18 ,925,491 bp, BDGP Release 6), which predicts a nonsense mutation in the open reading frame.
Nucleotide substitution: G18925491T.
G18925491T
E368term | Xrp1-PA; E368term | Xrp1-PB; E106term | Xrp1-PC; E106term | Xrp1-PD; E106term | Xrp1-PE; E368term | Xrp1-PF; E368term | Xrp1-PG
E?term
RpS3unspecified, Xrp1M2-73 has abnormal developmental rate phenotype, enhanceable by RpS12G97D/RpS12G97D
RpS174, Xrp1M2-73 has abnormal developmental rate phenotype, non-enhanceable by RpS12G97D
RpS174, Xrp1M2-73 has abnormal developmental rate phenotype, non-suppressible by RpS12G97D
Xrp1M2-73, RpS12G97D/RpS12G97D is a suppressor of abnormal developmental rate phenotype of RpS3unspecified
RpS174, Xrp1M2-73 has abnormal developmental rate phenotype
RpS3unspecified, Xrp1M2-73 has abnormal developmental rate phenotype