Nucleotide substitution: C?T. Amino acid replacement: L1412F.
C1024942T
C?T
L1412F | trio-PA; L1412F | trio-PC
L1412F
viable (with trioS036810)
visible (with trioS036810)
wing (with trioS036810)
4.8% of segments have thin/missing commissures and 5.1% of segment have commissures with pathfinding errors in trioIMP159.4/trioM89 embryos.
Heterozygotes with Df(3L)Fpa1 show mild irregularities in the commissures and longitudinal connectives of the embryonic central nervous system. Heterozygotes of trioS036810/trioM89 show a wing blister phenotype but are otherwise wild type.
trioM89/trioS036810 has partially lethal - majority live phenotype, enhanceable by seq9.17/seq[+]
trioM89/trioS036810 has some die during P-stage phenotype, enhanceable by seq9.17/seq[+]
trioM89/trioS036810 has lethal phenotype, enhanceable by Abl1/Abl[+]
trioM89/trioS036810 has lethal phenotype, enhanceable by Abl4/Abl[+]
trioM89/trioS036810 has lethal phenotype, enhanceable by faxM7/fax[+]
trioM89/trioS036810 has partially lethal - majority live phenotype, non-enhanceable by Df(2R)BSC273/+
trioM89/trioS036810 has some die during P-stage phenotype, non-enhanceable by Df(2R)BSC273/+
trioM89/trioS036810 has partially lethal - majority live phenotype, non-enhanceable by seqvr5-5/seq[+]
trioM89/trioS036810 has some die during P-stage phenotype, non-enhanceable by seqvr5-5/seq[+]
trioM89/trioS036810 has partially lethal - majority live phenotype, non-enhanceable by seq[+]/seqvr5-48
trioM89/trioS036810 has some die during P-stage phenotype, non-enhanceable by seq[+]/seqvr5-48
trioM89/trioIMP159.4 has abnormal neuroanatomy phenotype, non-enhanceable by fra4/fra[+]
Abl4/Abl1, Df(3L)Fpa1/trioM89 has abnormal neuroanatomy phenotype, suppressible | partially by ena[+]/enaGC10
Df(3L)Fpa1/trioM89 has lethal phenotype, suppressible | partially by ena[+]/enaGC10
trio[+]/trioM89 is an enhancer of abnormal neuroanatomy phenotype of Df(2R)vg135/fra4
trioM89/trioIMP159.4 is an enhancer of abnormal neuroanatomy phenotype of fra4
trio[+]/trioM89 is an enhancer of abnormal neuroanatomy phenotype of fra4
trioM89/trioS036810 is an enhancer of abnormal neuroanatomy phenotype of fra4
trioM89/trioIMP159.4 is an enhancer of abnormal neuroanatomy phenotype of Df(2R)vg135/fra4
trio[+]/trioM89 is an enhancer of lethal | prepupal stage phenotype of Abl4/Abl1
trio[+]/trioM89 is a suppressor of decreased occurrence of cell division phenotype of CycEJP
seq9.17/seq[+], trioM89/trioS036810 has abnormal feeding behavior phenotype
Abl4/Abl1, Df(3L)Fpa1/trioM89 has abnormal neuroanatomy phenotype
Df(3L)Fpa1/trioM89 has larval anterior commissure phenotype, enhanceable by Abl1/Abl[+]
Df(3L)Fpa1/trioM89 has larval longitudinal connective phenotype, enhanceable by Abl1/Abl[+]
Df(3L)Fpa1/trioM89 has larval posterior commissure phenotype, enhanceable by Abl1/Abl[+]
trioM89/trioS036810 has larval longitudinal connective phenotype, enhanceable by Abl1/Abl[+]
trioM89/trioIMP159.4 has symmetrical commissure phenotype, non-enhanceable by fra4/fra[+]
Abl4/Abl1, Df(3L)Fpa1/trioM89 has symmetrical commissure phenotype, suppressible | partially by ena[+]/enaGC10
trio[+]/trioM89 is an enhancer of symmetrical commissure phenotype of Df(2R)vg135/fra4
trioM89/trioIMP159.4 is an enhancer of symmetrical commissure phenotype of fra4
trio[+]/trioM89 is an enhancer of symmetrical commissure phenotype of fra4
trioM89/trioS036810 is an enhancer of symmetrical commissure phenotype of fra4
trioM89/trioIMP159.4 is an enhancer of symmetrical commissure phenotype of Df(2R)vg135/fra4
trio[+]/trioM89 is an enhancer of larval anterior commissure phenotype of Abl4/Abl1
trio[+]/trioM89 is an enhancer of larval longitudinal connective phenotype of Abl4/Abl1
trio[+]/trioM89 is an enhancer of larval posterior commissure phenotype of Abl4/Abl1
trioM89/trioIMP159.4 is a non-enhancer of larval longitudinal connective phenotype of Df(2R)vg135/fra4
Abl4/Abl1, Df(3L)Fpa1/trioM89 has symmetrical commissure phenotype
seq9.17 dominantly exacerbates the pre-pupal lethality of trioM89/trioS036810. However, survival to third instar larvae is indistinguishable between wild-type and the mutants. The seq9.17/+; trioM89/trioS036810 larvae retain the forager-like feeding behaviour at a time (90-93 hours after hatching) when their siblings and all control larvae have already transitioned to wanderers.
Dominantly suppresses the S phase defects seen in the CycEJP eye disc.
The suppression of prepupal lethality of trioM89/Df(3L)Fpa1 by enaGC10 is incomplete. Lethality is delayed until pupariation, but adults are never recovered.
Df(3L)Fpa1/trioM89 is rescued by trioUAS.cLa/Scer\GAL4sca-537.4