- Neomorph redirects here. It is also one of the post-human types of persons in the novel Eon by Greg Bear, as well as a creature from the movie Alien: Covenant.
Hermann J. Muller (1890–1967), who was a 1946 Nobel Prize winner, coined the terms amorph, hypomorph, hypermorph, antimorph and neomorph to classify mutations based on their behaviour in various genetic situations, as well as gene interaction between themselves. These classifications are still widely used in Drosophila genetics to describe mutations. For a more general description of mutations, see mutation, and for a discussion of allele interactions, see dominance relationship.
Key: In the following sections, alleles are referred to as +=wildtype, m=mutant, Df=gene deletion, Dp=gene duplication. Phenotypes are compared with '>', meaning 'phenotype is more severe than'
Loss of functionEdit
Amorphic describes a mutation that causes complete loss of gene function. Amorph is sometimes used interchangeably with "genetic null". An amorphic mutation might cause complete loss of protein function by disrupting translation ("protein null") and/or preventing transcription ("RNA null").
An amorphic allele elicits the same phenotype when homozygous and when heterozygous to a chromosomal deletion or deficiency that disrupts the same gene. This relationship can be represented as follows:
m/m = m/Df
An amorphic allele is commonly recessive to its wildtype counterpart. It is possible for an amorph to be dominant if the gene in question is required in two copies to elicit a normal phenotype (i.e. haploinsufficient).
Hypomorphic describes a mutation that causes a partial loss of gene function. A hypomorph is a reduction in gene function through reduced (protein, RNA) expression or reduced functional performance, but not a complete loss.
The phenotype of a hypomorph is more severe in trans to a deletion allele than when homozygous.
m/DF > m/m
Hypomorphs are usually recessive, but occasional alleles are dominant due to haploinsufficiency.
Gain of functionEdit
A hypermorphic mutation causes an increase in normal gene function. Hypermorphic alleles are gain of function alleles. A hypermorph can result from an increase in gene dose (a gene duplication), from increased mRNA or protein expression, or constitutive protein activity.
The phenotype of a hypermorph is worsened by increasing the wildtype gene dose, and is reduced by lowering wildtype gene dose.
m/Dp > m/+ > m/Df
m/m > m/Df > m/+ >>> +/Df > +/+ 
An antimorphic mutation might affect the function of a protein that acts as a dimer so that a dimer consisting of one normal and one mutated protein is no longer functional.
A neomorphic mutation causes a dominant gain of gene function that is different from the normal function. A neomorphic mutation can cause ectopic mRNA or protein expression, or new protein functions from altered protein structure.
Changing wildtype gene dose has no effect on the phenotype of a neomorph.
m/Df = m/+ = m/Dp
m/Df = m/Dp
- Muller’s classification of mutant alleles
|Wild type||Referent gene expression, full ("normal"), expression of parent allele|
|Amorph||Dysfunctional, with null expression|
|Hypomorph||Reduced, or partial reduced gene activity|
|Hypermorph||Increased or partial increased parent gene activity|
|Neomorph||Novel function, comparing with the initial, new property|
|Antimorph||Opposing, antagonizing, or interfering gene activity|
|Isomorph||Identical expression with original (parent) allele, mostly resulting from silent point mutations|
- Muller, H. J. 1932. Further studies on the nature and causes of gene mutations. Proceedings of the 6th International Congress of Genetics, pp. 213–255.
- Wilkie, A. O. 1994. The molecular basis of genetic dominance. Journal of Medical Genetics 31: 89-98. 
- Hawley R. S., Walker Y.M. (2003) Advanced Genetic Analysis: Finding Meaning in a Genome, pp. 6-7, ISBN 1405123923
- Lawrence E., ed. (1999). Henderson's Dictionary of biological terms. London: Longman Group Ltd. ISBN 0-582-22708-9.
- Rieger R. Michaelis A., Green M. M. (1976). Glossary of genetics and cytogenetics: Classical and molecular. Berlin - Heidelberg - New York: Springer-Verlag. ISBN 3-540-07668-9.CS1 maint: Uses authors parameter (link)