Amino acid replacement: S201L.
Nucleotide substitution: C?T.
Atpα protein expression levels are not significantly altered in heterozygotes.
C20964472T
C?T
S240L | Atpalpha-PA; S201L | Atpalpha-PB; S201L | Atpalpha-PC; S201L | Atpalpha-PD; S201L | Atpalpha-PE; S201L | Atpalpha-PF; S201L | Atpalpha-PG; S201L | Atpalpha-PH; S201L | Atpalpha-PI; S201L | Atpalpha-PJ; S201L | Atpalpha-PK
S201L
Heterozygotes are bang sensitive.
AtpαCJ5/AtpαCJ7 animals are aphenotypic at 25[o]C, but surviving adults at 29[o]C are bang-sensitive.
Heterozygotes display normal waking activity levels - i.e., normal circadian rhythms.
Heterozygotes display reduced waking locomotor activity in response to startle stimulation.
Aged heterozygous adult brains exhibit mild neuropathology.
Aged heterozygous flight muscle does not exhibit myopathology.
Heterozygous mutants have a significantly lower respiration (metabolic) rate than controls.
Homozygous embryos form normal paracellular barriers and trachea.
Young heterozygous adults display no overt locomotor defects. However, these flies show significant, progressive bang sensitivity as they age.
Heterozygotes have a lifespan similar to controls.
Heterozygous adults do not show a marked reduction in feeding.
Separable from: A recessive lethal unlinked to Atpα.