Polytene chromosomes normal.
Point mutation.
UAG stop codon in mII. Inactivates Ubx isoforms Ia/b and IIa/b, but not IVa.
Mutation causing a stop codon in the third Ubx exon.
Single nucleotide change that introduces a nonsense codon in the exon at -53kb.
Amino acid replacement: ??term.
Nucleotide substitution: G?A.
Point mutation in the -50kb microexon, which generates a nonsense codon in the open reading frame of transcripts that use this microexon. Proteins encoded by these transcripts should terminate 7 amino acids before the start of the homeobox.
G16710567A
TGG?TAG
W288term | Ubx-PA; W271term | Ubx-PC; W262term | Ubx-PD; W279term | Ubx-PE
W?term
Position of mutation on reference sequence inferred by FlyBase curator based on author statement. See Figure 2c of FBrf0046283. Nonsense codon only causes termination in transcripts which use this exon. These transcripts should terminate 7 amino acids before the start of the homeobox.
chordotonal organ & axon
Keilin's organ & abdominal segment 1
peripheral nervous system & parasegment 5
peripheral nervous system & parasegment 6
Denticle belts of the third thoracic segment and the first abdominal segment are transformed to resemble those of the second thoracic segment.
Haltere enlarged, average bristle number 0.8 (+-1.2 (SD); N=252).
Transformation of the PNS patterns of parasegment 5 and 6 into copies of that of parasegment 4.
Heterozygotes for Ubx195 and a bxd breakpoint mutation show complete T3p to T2p ("pbx") and A1a to T3a ("bxd") transformations.
Like Ubx1.
Does not affect the frequency of the trx bithorax-variegated phenotype in heterozygous combination with Df(3R)red-P52.
Transvection positive with Ubxbx-34e.
Homozygotes complete embryogenesis and occasionally survive as third instar larvae. They have the characteristic Ubx phenotype of transformed denticle belts and three pairs of anterior spiracles. Ubx195/Ubxabx-2 transheterozygotes show extensive transformations of second thoracic leg to first leg structures. Many Ubx195/Ubxbxd-100 or Ubx195 /Ubxabx-2 flies eclose. Ubx195 in trans with abx or bxd alleles has virtually no effect on the development of the adult nervous system; the pattern of commissures is indistinguishable from wild-type in Ubx195/Ubxbxd-100 adults. In Ubx61d/Ubxbxd-100 larvae A1 is transformed to T3, and a pair of presumptive leg neuromeres is formed in this transformed segment.
Ubx195 has phenotype, enhanceable by Hrb27C10280
Ubx195 has haltere sensillum phenotype, enhanceable by Df(1)HC244
Ubx195 has haltere sensillum phenotype, enhanceable by Df(1)Sxl-bt
Ubx195 has haltere sensillum phenotype, enhanceable by Df(1)KA14
Ubx195 has haltere sensillum phenotype, enhanceable by Df(1)C246
Ubx195 has haltere sensillum phenotype, enhanceable by Df(1)sd72b
Ubx195 has haltere sensillum phenotype, enhanceable by Df(1)N19
Ubx195 has haltere sensillum phenotype, enhanceable by Df(1)HF396
Ubx195 has haltere sensillum phenotype, enhanceable by Df(2L)dp-79b
Ubx195 has haltere sensillum phenotype, enhanceable by Df(2L)TE29Aa-11
Ubx195 has haltere sensillum phenotype, enhanceable by Df(2L)Mdh
Ubx195 has haltere sensillum phenotype, enhanceable by Df(2L)Prl
Ubx195 has haltere sensillum phenotype, enhanceable by Df(2L)TW203
Ubx195 has haltere sensillum phenotype, enhanceable by Df(2L)TW158
Ubx195 has haltere sensillum phenotype, enhanceable by Df(2L)TW84
Ubx195 has haltere sensillum phenotype, enhanceable by Df(3L)pbl-X1
Ubx195 has haltere sensillum phenotype, enhanceable by Df(3L)pbl-NR
Ubx195 has haltere sensillum phenotype, enhanceable by Df(3L)Rdl-2
Ubx195 has haltere sensillum phenotype, enhanceable by Df(3L)29A6
Ubx195 has haltere sensillum phenotype, enhanceable by Df(3L)fz-D21
Ubx195 has haltere sensillum phenotype, enhanceable by Df(3L)fz-M21
Ubx195 has haltere sensillum phenotype, enhanceable by Df(3L)brm11
Ubx195 has haltere sensillum phenotype, enhanceable by Df(3L)st-f13
Ubx195 has haltere sensillum phenotype, enhanceable by Df(3L)ri-79c
Ubx195 has haltere sensillum phenotype, enhanceable by Df(3R)ME15
Ubx195 has haltere sensillum phenotype, enhanceable by Df(3R)9A99
Ubx195 has haltere sensillum phenotype, enhanceable by Df(3R)Antp17
Ubx195 has haltere sensillum phenotype, enhanceable by Df(3R)by10
Ubx195 has haltere sensillum phenotype, enhanceable by Df(3R)by62
Ubx195 has haltere sensillum phenotype, enhanceable by Df(3R)M-Kx1
Ubx195 has haltere sensillum phenotype, enhanceable by Df(3R)M86D
Ubx195 has haltere sensillum phenotype, enhanceable by crn3
Ubx195 has haltere sensillum phenotype, enhanceable by Df(3R)Delta-BX12
Ubx195 has haltere sensillum phenotype, enhanceable by Df(3R)crb87-4
Ubx195 has haltere sensillum phenotype, enhanceable by Df(3R)crb87-5
Ubx195 has haltere sensillum phenotype, enhanceable by Df(3R)X3F
Ubx195 has haltere sensillum phenotype, enhanceable by Df(3R)awd-KRB
Ubx195 has haltere sensillum phenotype, enhanceable by Df(4)G
Ubx195 has haltere sensillum phenotype, enhanceable by Hrb27C[+]/Hrb27C10280
Ubx195 has haltere sensillum phenotype, enhanceable by crn4
Ubx195 has haltere sensillum phenotype, enhanceable by kz26
Ubx195 has haltere sensillum phenotype, enhanceable by Df(1)64c18
Ubx195 has haltere sensillum phenotype, enhanceable by Df(1)JC19
Ubx195 has haltere sensillum phenotype, enhanceable by Df(1)dm75e19
Ubx195 has phenotype, non-enhanceable by Df(3R)ry506-85C
Ubx195 has haltere phenotype, suppressible by Df(3R)l26c
Ubx195 has phenotype, non-suppressible by Df(3R)ry506-85C
Hrb27C10280 enhances the haltere phenotype of Ubx195/+ such that halteres are enlarged, and average bristle number 3.6 (+-1.6 (SD); N=50).
Lewis, Jan. 1968.
The phenotype of a number of combinations of Ubx mutations has been investigated to determine the role of the bxd regulatory region in the modulation of Ubx expression.
Phenotype in the PNS is qualitatively and quantitatively identical to that for complete absence of Ubx function.