Construct: Amino acid replacement: Q70@.
C9694881T
Q70term | btd-PA
Q70term
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
Type II neuroblasts in homozygous clones in the larval brain maintain a type II neuroblast marker expression profile. They appear to generate non-functional ase[-] immature intermediate neural progenitors that likely adopt an identity of ganglion mother cells normally found in the type I neuroblast lineage.
Homozygous embryos fail to form a cephalic furrow. The ventral furrow and proctodeal invagination form normally. No signs of initiator cell activity are seen between the beginning of cycle 14 and stage 7.
The lateral pentascolopidial chordotonal organs (lch5) in the abdominal segments contain an average of 3 to 4 scolopidia in mutant embryos.
A weak allele of btd. Mandibular, intercalary and antennal segments absent.
btdXA is a suppressor | somatic clone of abnormal neuroanatomy | somatic clone | larval stage phenotype of bratunspecified
btdXA is a suppressor | somatic clone of type II neuroblast | increased number | somatic clone | larval stage phenotype of bratunspecified
btdXA ; bratunspecified double mutant clones in the larval brain do not lead to supernumerary neuroblast formation.
btdXA is rescued by btdRV-2ndB
btdXA is not rescued by btdFRT.RV-2ndB