Nucleotide substitution: G11292A. Amino acid replacement: C739Y.
G3164844A
G11292A
C739Y | N-PA; C739Y | N-PB
C739Y
Site of nucleotide substitution in mutant inferred by FlyBase based on reported amino acid change.
adult thorax & microchaeta
adult thorax & microchaeta (with Nl1N-ts1)
adult thorax & microchaeta | somatic clone
Heterozygotes show loss of thoracic microchaetae, having 89.25 +/- 1.90 thoracic microchaetae per heminotum (compared to the wild-type number of 130.35 +/- 1.54). 99% of thoracic microchaetae are missing in homozygous clones, whereas macrochaetae are unaffected. Animals carrying 1 copy of NMcd5 in the presence of 2 copies of N+ have 114.83 +/- 2.58 thoracic microchaetae per heminotum. Animals carrying 2 copies of NMcd5 in the presence of 1 copy of N+ have 72.92 +/- 2.44 thoracic microchaetae per heminotum. NMcd5/Nl1N-ts1 flies have 36.75 +/- 1.88 thoracic microchaetae per heminotum. Homozygous pupae show loss of microchaetae precursors in the thorax.
NMcd5 has visible | dominant phenotype, enhanceable by Su(H)[+]/Su(H)IB115
DeltaRevF10, NMcd5, SerRX82 has visible | somatic clone phenotype
NMcd5, Su(H)IB115 has visible | somatic clone phenotype
Deltaunspecified, NMcd5 has visible | somatic clone phenotype
Df(3R)grob32.2, NMcd5 has visible | somatic clone phenotype
NMcd5 has adult thorax & microchaeta phenotype, enhanceable by Su(H)[+]/Su(H)IB115
DeltaRevF10, NMcd5, SerRX82 has microchaeta | somatic clone phenotype
NMcd5, Su(H)IB115 has microchaeta | somatic clone phenotype
Deltaunspecified, NMcd5 has microchaeta | somatic clone phenotype
Df(3R)grob32.2, NMcd5 has microchaeta | somatic clone phenotype
NMcd5 Dlunspecified double mutant clones do not develop microchaetae but produce epidermis. NMcd5 DlRevF10 SerRX82 triple mutant clones do not develop microchaetae but produce epidermis. NMcd5 Su(H)IB115 double mutant clones do not develop microchaetae but produce epidermis. Df(3R)grob32.2 double mutant clones do not develop microchaetae but produce epidermis. Macrochaetae in NMcd5 DlRevF10 double mutant clones develop as single bristles rather than as a neurogenic tuft. dxENU and dxP dominantly suppress the loss of microchaetae seen in NMcd5 heterozygotes, increasing the number of microchaetae per heminotum to 94.25 +/- 1.15 and 105.33 +/- 3.08 respectively. Su(H)IB115 dominantly enhances the loss of microchaetae seen in NMcd5 heterozygotes, reducing the number of microchaetae per heminotum to 69.92 +/- 1.86.