From Wikipedia, the free encyclopedia.
For other non-genetic uses of the term "dominance", see Dominance.
In genetics, dominance relationships are the ways genes interact to express themselves as phenotypes in an individual. There are three kinds of dominance relationships.
Simple dominance
Simple dominance occurs when one gene's allele is completely dominant over another, recessive allele. The individual is thus a carrier of the recessive gene but the recessive gene is not expressed at all; however, a recessive gene may still be passed on through reproduction and have an opportunity to express itself in a later generation. If both parents carry a recessive gene, their parents should inherit the gene. 1 For dominant traits, people either have it or not. There is no in-between. Also, most genes have more than two alleles, which can have all sorts of dominance relationships.
This can be expressed by a diagram called a Punnett square. It looks like this:
| b | B | |
| B | Bb | BB |
| b | bb | bB |
In this example, B represents the dominant brown-eye gene and b the recessive blue-eye gene. In the BB, Bb and bB cases, the child has brown eyes due to the dominant B. Only in the bb case does the recessive blue-eye trait express itself in the blue-eye phenotype. So in this fictional case, statistically one quarter of this couple's children will have blue eyes and the rest will have brown eyes. Ideally, for this to occur, a large number of people are necessary.
Traits governed by this relationship: (not an exhaustive list)
| Dominant | Recessive |
| Brown Eyes | Blue Eyes |
| Curled Up Nose | Roman Nose |
| Clockwise Hair Whorl | Counter-clockwise Hair Whorl |
| Can Roll Tongue | Can't Roll Tongue |
| Widow's Peak | No Widow's Peak |
Some genetic diseases carried by dominant and recessive alleles:
| Disease | Gene is... |
| Polydactylism | dominant |
| Marfan syndrome | dominant |
| Some types of Dwarfism | recessive |
| Tay-Sachs disease | recessive |
As can be seen from this, dominant alleles are not necessarily more common or more desirable.
This relationship has the same effects as above for homozygous individuals. For heterozygous individuals, the dominant and recessive traits blend into a middle ground.
The classic example of this is the colours of carnation flowers.
Genetic diseases governed by this relationship:
Incomplete dominance
R w
R RR Rw
w wR ww
R is red, w is white. Rw is pink, since red is incompletely dominant over white.
| Name | Gene is incompletely |
| Brachydactyly | dominant2 |
| Sickle cell anemia | recessive3 |
For these examples, the homozygous traits are more serious than the heterozygous trait. In fact, carriers of SCA are better off!
Co-dominance
In co-dominance, neither phenotype is dominant. Instead, the individual expresses BOTH phenotypes. The most important example is in Landsteiner blood groups.
The gene for blood types has three alleles: A, B, and i. i causes O type and is recessive to both A and B. When a person has both A and B, they have type AB blood.
Example Punnett square for a father with A and i, and a mother with B and i:
| A | i | |
| B | AB | B |
| i | A | O |
There are very few (if any) co-dominant genetic diseases and very few other traits.
Notes

