Concept cluster: Biology > Genetic mutation
n
(genetics) a null mutation.
n
(genetics) A mutation that restores the original sequence and hence the original phenotype.
v
Alternative form of coamplify [(genetics) (of the gene) to amplify together with another gene, or to amplify in multiple ways]
n
The creation of epimutations
n
Any organism formed by epimutation
adj
That has undergone epimutation
n
frameshift mutation
n
(biology) An organism that has seven mutations
n
(genetics) Excessive editing (of nucleic acid)
n
(genetics) a gain of function mutation that causes an increase in otherwise normal gene function.
adj
(genetics, of a mutation) causing an increase in otherwise normal gene function.
v
To cause, or to undergo hypermutation
adj
That have undergone hypermutation
n
(countable) The organism or gene that results from such a mutation
n
(genetics) Any agent that causes hypermutation
n
(biology) A reduced rate of mutation
n
(genetics) Any agent that causes hypomutation
n
(evolutionary genetics) The process by which the genomes of an asexual population accumulate deleterious mutations in an irreversible manner; proposed as a theory to explain the evolution of sex.
n
Any agent or substance that can cause genetic mutation.
v
(genetics) To cause mutation.
n
All the somatic mutations associated with a tumour
n
(genetics) That has mutated, with one or more new characteristics from a mutation.
n
(biochemistry, genetics) Any protein produced via a mutated gene
n
(genetics) Any heritable change of the base-pair sequence of genetic material.
n
(genetics) The process by which a small population accumulates harmful mutations, which leads to loss of fitness and decline of the population size, which may lead to further accumulation of deleterious mutations due to fixation by genetic drift.
n
(genetics) A unit of mutation forming part of a recon.
n
(genetics) A gain of function mutation that causes novel gene function.
adj
(genetics, of a mutation) causing a novel gene function.
n
A mutation that has not been previously described / recorded
n
An organism that has a paramutation
adj
Modified by paramutation
n
(genetics) A mutation in which a heritable change in one allele is induced by another in the same locus
n
(genetics) A group of five mutations
n
(genetics) A mutation that involves the replacement, addition or deletion of a small number of bases (especially just one) at a specific site within a gene.
n
A nucleotide sequence variation that is not enough to be classed as a mutation (for example, does not affect protein expression enough to produce clinical symptoms) but nonetheless represents an unusual variant that is predisposed to still greater variation in future cell divisions (that is, predisposed to leading to a mutation).
n
(genetics) The situation in which the inheritance of a recessive trait mimics a dominant pattern.
n
Such a mutant
n
(genetics) A rescued mutation, typically in a virus.
v
(genetics) To cause or to undergo retrohoming
n
(genetics) The condition of being retromobile
n
(genetics) mutation to a previous (typically an original) form
adj
Of or pertaining to retrotransposons
adj
(genetics) That has reverted to its former genotype or to the original phenotype by means of a subsequent mutation
n
(genetics) A mutant that contains one and a half times the amount of an original characteristic
n
(genetic engineering) A proposed kind of modified seed whose use would be restricted by having important genes activated only in response to some stimulus (such as a special chemical), and which would otherwise produce infertile second-generation seeds.
n
(genetics) An amalgamation of characters that respond to the same selective pressure.
n
(genetics) A gene that has four mutations (often of the same type at different locations)
n
(genetics) The alteration of a bacterial cell caused by the transfer of DNA from another, especially if pathogenic.
adj
(genetics) Between hemizygous organisms
n
(genetics) A point mutation in which one base is replaced by another of the same class (purine or pyrimidine); compare transversion.
v
(genetics, transitive, of a chromosomal segment) To cause to undergo translocation.
adj
That regulates transfection
n
(genetics) A point mutation in which a purine is replaced with a pyrimidine, or vice versa
adj
(biology) having three mutations
n
(biology) A very high level of mutation
adj
(genetics) Not expressed to the usual or expected degree

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