Nonsense mutation.
C15312097T
C593T|FBrf0124909
Q84term | Xpc-PA; Q85term | Xpc-PC; Q85term | Xpc-PD
Amino acid change coordinates are for Xpc- PA
Homozygous larvae derived from homozygous females show greater sensitivity to methyl methanesulfonate (MMS) than homozygous larvae derived from heterozygous females.
Larval survival hypersensitive to exposure to methyl methanesulfonate, N-acetyl-2-aminofluorene, and benzoapyrene, moderately sensitive to nitrogen mustard and insensitive to gamma rays. Excision of pyrimidine dimers impaired; 4-5 fold decrease in activity of ultra-violet-specific endonuclease observed in primary cell cultures.
XpcB1, mus201D1 has chemical sensitive phenotype
XpcB1, mus211B1 has chemical sensitive phenotype
PolZ1A1, XpcB1, mus208B1 has chemical sensitive phenotype
XpcB1, mus208B1 has chemical sensitive phenotype
XpcB1, mus208B1, mus211B2 has chemical sensitive phenotype
PolZ1B1, XpcB1, mus208B1 has chemical sensitive phenotype
Viable in double homozygous combination with mus201D1, mus205B1, mus208B1 or mus211B1. mus208B1 mus210B1 mus211B1 triple homozygotes show 89% viability compared to controls. mus208B1 mus210B1 mus211B2 triple homozygotes show 88% viability compared to controls. mus205B1 mus210B1 double mutant larvae are no more sensitive to MMS than mus205B1 single mutant larvae. mus210B1 and mus211B1 show a fairly strong synergistic interaction with respect to sensitivity to methanesulfonate (MMS). mus201D1 shows a fairly strong synergistic interaction with respect to sensitivity to methanesulfonate (MMS) in combination with either mus208B1 or mus210B1. mus208B1 mus210B1 mus211B2 triple homozygotes are sensitive to MMS, ethyl methanesulfonate, N-nitrosodimethylamine, diethylnitrosamine, nitrosomethyl urea and N-methyl-N'-nitro-N-nitrosoguanidine, formaldehyde, cyclophosphamide, diepoxybutane, benzoapyrene, benzoepyrene and hexamethylphosphoramide compared to controls. mus205B1 mus208B1 mus210B1 triple homozygotes are sensitive to MMS, ethyl methanesulfonate, N-nitrosodimethylamine and diethylnitrosamine compared to controls.