Imprecise excision of P{GawB}Trim9NP4638 (located 152bp upstream of the start codon of Trim9) generates a deletion within the 5'UTR and further upstream of Trim9.
Trim946 has abnormal neuroanatomy phenotype, enhanceable by fra3/Df(1)NP5/fra[+]/+
Trim946 has abnormal neuroanatomy phenotype, suppressible by robo[+]/Df(2R)BSC482/robo11/+
Trim946 has abnormal neuroanatomy phenotype, suppressible by fraUAS.cKa/Scer\GAL4ppk.1.9
Trim946 has dopaminergic neuron phenotype, enhanceable by fra3/Df(1)NP5/fra[+]/+
Trim946 has commissure phenotype, enhanceable by robo[+]/fra3/robo11/fra[+]
Trim946 has dopaminergic neuron phenotype, suppressible by robo[+]/Df(2R)BSC482/robo11/+
+:, Trim946 has commissure phenotype, suppressible by Df(2R)BSC482/Df(1)NP5/+/+
Trim946 has dopaminergic neuron phenotype, suppressible by fraUAS.cKa/Scer\GAL4ppk.1.9
Trim946 has commissure phenotype, suppressible by fraUAS.cKa/Scer\GAL4ppk.1.9
The Trim946 axon midline crossing phenotype is significantly enhanced in a Df(1)NP5 and fra3 heterozygous background.
Removal of one copy of robo1 and sli (using the deficiency Df(2R)BSC482) suppresses the axon midline crossing defect found in Trim946 mutants.
Overexpression of fraScer\UAS.cKa under the control of Scer\GAL4ppk.1.9 significantly suppresses the Trim946 midline crossing defects.
Trim946 is rescued by Trim9UAS.cSa/Scer\GAL4ppk.1.9
Expression of Trim9Scer\UAS.cSa in class IV da neurons under the control of Scer\GAL4ppk.1.9 fully rescues the guidance defects found in Trim946 mutants.