Amino acid replacement: K28A.
Substitution of a conserved lysine at position 28 in the predicted catalytic domain with alanine, resulting in a catalytically dead mutant protein.
AA17040928GC
K28A | Trm7-32-PA
K28A
Trm7-32K28A homozygotes survive until adulthood under standard conditions, without major growth defects or significant developmental delays, but adults are sluggish and short lived. However, they show increased viral load upon infection with Drosophila C Virus, as compared to controls.
Trm7-32K28A has short lived phenotype, non-enhanceable by Trm7-34e02001/Trm7-34e02001
Trm7-32K28A has abnormal locomotor behavior | adult stage | recessive phenotype, non-enhanceable by Trm7-34e02001/Trm7-34e02001
Trm7-32K28A has short lived phenotype, non-suppressible by Trm7-34e02001/Trm7-34e02001
Trm7-32K28A has abnormal locomotor behavior | recessive | adult stage phenotype, non-suppressible by Trm7-34e02001/Trm7-34e02001
Trm7-32K28A/Trm7-32K28A is a non-enhancer of abnormal locomotor behavior | adult stage | recessive phenotype of Trm7-34e02001
Trm7-32K28A/Trm7-32K28A is a non-suppressor of abnormal locomotor behavior | recessive | adult stage phenotype of Trm7-34e02001
Trm7-32K28A, Trm7-34e02001 has viable phenotype
Trm7-32K28A, Trm7-34e02001 has decreased body size phenotype
Trm7-34e02001, Trm7-32K28A double homozygotes show a measurable reduction in size and weight when compared to controls.