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Mutation
A heritable change in the DNA sequence of an organism.
Mutant
An organism resulting from a mutation with a recognizable change in phenotype compared to the wild type.
Wild Type
The phenotype most commonly observed in nature.
Point Mutation
A mutation affecting only one or a few nucleotides in a gene.
Silent Mutation
A point mutation that results in the same amino acid being incorporated into the resulting polypeptide, having no effect on the protein's structure.
Missense Mutation
A mutation that results in a different amino acid being incorporated into the resulting polypeptide.
Nonsense Mutation
A point mutation that converts a sense codon to a stop codon, resulting in shorter and typically nonfunctional proteins.
Frameshift Mutation
A mutation caused by insertions or deletions of nucleotides that are not in multiples of three, leading to a shift in the reading frame.
Proofreading
A DNA replication mechanism in which DNA polymerase corrects mistakes by replacing incorrect bases.
Ames Test
A rapid screening method using bacteria to determine the carcinogenic potential of new chemical compounds.