Amino acid replacement: G149S.
Amino acid replacement: M181T.
Amino acid replacement: F229L.
T11284919C
F229L | Osi21-PA
F229L
A nucleotide change at the first or third position of the Phe codon leads to a Leu mutation (base change unspecified).
T11285062C
M181T | Osi21-PA
M181T
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
G11285159A
G149S | Osi21-PA
G149S
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
lethal (with Df(2L)Exel8005)
viable (with Df(2L)Exel6028)
Osi21MB01450/Osi21die4 is a suppressor of increased cell death | conditional phenotype of norpAP24
Osi21die4/Osi21die4 is a suppressor of increased cell death | conditional phenotype of rdgC306
Osi21die4/Osi21die4 is a suppressor of increased cell death | conditional phenotype of trp1
Osi21die4/Osi21die4 is a non-suppressor of increased cell death | conditional phenotype of rdgB2
Osi21+tLa, Osi21MB01450/Osi21die4, norpAP24 has increased cell death | conditional phenotype
Osi21+tLa, Osi21MB01450/Osi21die4, norpAP24 has retina | conditional phenotype
Osi21die4/Osi21die4, Osi21die4/Df(2L)Exel6028 or Osi21die4/Osi21MB01450 (but not Osi21die4/Osi21MB01450;Osi21+tLa) partially suppresses the progressive retinal degeneration seen under constant light exposure in norpA36/norpA36 flies. Osi21die4/Osi21die4 partially suppresses the progressive retinal degeneration seen under constant light exposure in trp1/trp1 or rdgC306/rdgC306 (but not rdgB2/rdgB2) flies.
The retinal degeneration (loss of deep pseudopupil) seen in norpA36 flies after 5 days in constant light is suppressed if the eyes are homozygous for diehard4diehard4.
Separable from: a secondary lethal mutation; the chromosome is homozygous lethal, but is viable over a deficiency (Df(2L)Exel6028) that uncovers Osi21 (the Osi21die4/Df(2L)Exel6028 combination shows the suppression of norpA36 retinal degeneration, as expected).