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D3.3 · Explain genotype, phenotype, dominance, and other inheritance patterns
Learn to explain genotype, phenotype, dominance, and other inheritance patterns through clear examples and targeted practice.
Ontario Grade 11 Biology
Genetic Processes
How allele combinations relate to traits
In SNC2D, you learned that cells are the basic units of life and that organisms inherit information from their parents. In this lesson, we will use a simple model to describe how inherited versions of a gene can relate to an observable trait. For example, a plant may have purple or white flowers. The visible flower colour is its phenotype. The allele combination used to describe that colour is its genotype. Genetic models help explain patterns in families, but a probability for a child or offspring is not a guarantee of what will happen in one particular case.
What you will learn
- Distinguish genotype from phenotype.
- Explain how dominance affects the phenotype linked to a genotype.
- Use a Punnett square to predict possible offspring genotypes and phenotypes.
- Compare complete dominance, incomplete dominance, codominance, and inheritance involving multiple alleles.
From inherited information to a trait
A gene is a unit of inherited information associated with a trait. An allele is one version of a gene. For a basic inheritance model, an organism receives one allele from each parent. The two alleles together make its genotype for that gene.
A genotype is the allele combination an organism has. A phenotype is the observable form of a trait, such as a flower's colour. Some phenotypes are visible; others can be described in different ways. Phenotype refers to the trait, not the allele combination.
For a simple example, imagine a flower-colour gene with a purple allele and a white allele. We can use for the purple allele and for the white allele. These letters are a model's labels; they do not show how a gene works inside a cell.
An organism with two matching alleles is homozygous for that gene. An organism with two different alleles is heterozygous. Thus, and are homozygous genotypes, while is heterozygous.
- Genotype means the allele combination.
- Phenotype means the observable trait.
- Homozygous means two matching alleles; heterozygous means two different alleles.
Dominance and a simple inheritance model
In complete dominance, one allele is dominant over another for a particular trait. The dominant allele determines the phenotype in a heterozygous organism. The other allele is called recessive. A recessive phenotype appears only when the organism has two recessive alleles in this simple model.
For the flower example, suppose purple is completely dominant to white. Then and have purple flowers, while has white flowers. Dominant does not mean more common, stronger, or better. It describes how the alleles relate to a phenotype in this model.
A Punnett square is a grid used to list possible allele combinations in offspring. Each parent contributes one allele. If both parents have genotype , each can contribute or . The four equally likely combinations in the model are , , , and .
The square predicts a 1 in 4 chance of , a 2 in 4 chance of , and a 1 in 4 chance of . With complete dominance, that corresponds to a 3 in 4 chance of purple and a 1 in 4 chance of white. These are probabilities across possible offspring, not a promise about a particular offspring or a small group.
- Dominance describes the phenotype relationship between alleles.
- Punnett squares list possible genotypes from parental alleles.
- A predicted probability is not certainty for an individual offspring.
Other inheritance patterns
Not every trait follows complete dominance. In incomplete dominance, neither allele completely masks the other in a heterozygote. The heterozygote has an intermediate phenotype. For instance, if a red-flowered plant and a white-flowered plant produce pink-flowered heterozygotes, pink is intermediate between red and white.
In codominance, both alleles are expressed in the heterozygote. The phenotype shows both forms rather than blending them into an intermediate. Human AB blood type is an example: the A and B alleles are both expressed in a person with blood type AB.
Some genes have more than two alleles in a population. This is called multiple-allele inheritance. Each individual still has only two alleles for that gene in the simple model. The ABO blood group system has three common alleles: , , and . The A and B alleles are codominant to each other, and each is dominant over .
These patterns are models for describing observed inheritance. The same labels do not mean every trait follows the same pattern. To choose a pattern, look at the relationship between genotype and phenotype given in the question or supported by observations.
- Incomplete dominance produces an intermediate heterozygous phenotype.
- Codominance means both alleles are expressed in the heterozygote.
- Multiple alleles means more than two allele forms exist in a population, not that one individual has more than two.
Using and evaluating inheritance models
Begin with the information given about a trait. Identify the alleles and determine the stated inheritance pattern. Then connect each genotype to its phenotype. If parents' genotypes are known, list the allele each parent could pass on and combine the possibilities in a Punnett square.
An inheritance model is useful because it makes predictions clear and testable. Still, a model is not the same as an observation. A family may show a pattern that fits a model, but a small number of observations cannot prove that every future case will match it. Use the information in the question and avoid claiming more than the model supports.
Keep the key terms separate. A genotype is not a phenotype. A dominant allele is not necessarily common. And a probability describes possible outcomes across repeated cases; it does not tell with certainty which outcome one offspring will have.
- Use the stated genotype-to-phenotype rules before predicting outcomes.
- Treat a Punnett square as a probability model, not a guarantee.
- Distinguish an observed pattern from the model used to explain it.
How common inheritance patterns differ
| Pattern | Heterozygous phenotype | Example used here |
|---|---|---|
| Complete dominance | Shows the dominant allele's phenotype | Pp is purple |
| Incomplete dominance | Intermediate between the two forms | RW is pink |
| Codominance | Both allele forms are expressed | I^A I^B is type AB |
| Multiple alleles | More than two allele forms occur in the population | ABO has I^A, I^B, and i |
Worked example
Complete dominance in flowers
In a plant species, purple flowers () are completely dominant to white flowers (). Predict the possible genotypes and phenotypes for offspring of two heterozygous plants.
- Identify parental allelesEach parent has genotype , so each can pass on either or . Each offspring receives one allele from each parent.
- List combinationsPair each possible allele from one parent with each possible allele from the other. The combinations are , , , and . PP,\ Pp,\ Pp,\ pp
- Connect genotype to phenotypeThe complete-dominance rule makes both and purple. Only is white. Therefore, three of the four equally likely outcomes are purple and one is white.
Answer: The genotype ratio is 1 :2 :1 . The phenotype probability is 3 in 4 purple and 1 in 4 white.
Check: A single offspring is not guaranteed to have purple flowers; the fractions describe the model's probabilities.
Worked example
Incomplete dominance
For a flower trait, suppose is associated with red and with white. Heterozygotes are pink. Predict the offspring of a pink plant crossed with a white plant.
- Represent the parentsUnder the stated pattern, pink is the heterozygous genotype , and white is . The pink parent can pass on or ; the white parent can pass on only .
- Combine possible allelesCombining the options gives and in equal proportions. There is no combination in this cross. RW,\ RW,\ WW,\ WW
- Interpret the outcomesThe problem states that is pink and is white. The predicted probabilities are therefore one-half pink and one-half white.
Answer: The offspring have a 1 in 2 probability of being pink and a 1 in 2 probability of being white.
Check: Pink is intermediate here because the question specifies incomplete dominance; do not apply the complete-dominance rule.
Worked example
ABO blood group alleles
A parent with genotype and a parent with genotype have a child. Find the possible blood-group phenotypes and their probabilities in the model.
- List parental contributionsThe first parent can pass on or . The second can pass on or . Each combination is equally likely in this model.
- Form possible genotypesCombining the contributions gives , , , and . Each occurs in one of the four equally likely combinations.
- Use the allele relationshipsand are codominant, so gives type AB. Each is dominant over , so is type A and is type B. The genotype gives type O.
Answer: The model predicts a one-quarter probability for each of blood types A, B, AB, and O.
Check: An individual has two alleles in this example, even though three allele forms occur in the population.
Common mistakes and how to avoid them
Calling the visible trait a genotype.
Correction: The visible trait is the phenotype. The allele combination is the genotype.
Assuming a dominant allele must be the most common allele.
Correction: Dominance describes how an allele affects the heterozygous phenotype in a model. It does not state how common the allele is.
Assuming every heterozygote shows complete dominance.
Correction: Check the inheritance pattern. A heterozygote may show an intermediate phenotype or both allele forms.
Treating a Punnett-square probability as a guaranteed outcome.
Correction: A probability describes possible outcomes. It cannot determine with certainty the genotype or phenotype of one offspring.
Lesson summary
- Genotype is an allele combination; phenotype is an observable trait.
- In complete dominance, a dominant allele determines the heterozygous phenotype.
- Incomplete dominance gives an intermediate heterozygous phenotype; codominance expresses both allele forms.
- Multiple alleles can exist in a population, while an individual in the simple model has two alleles for the gene.
- Punnett squares organize possible outcomes and probabilities, not certainties.
Check your understanding
Question 1
In a complete-dominance model, is dominant to . Which genotype is heterozygous?
- The phenotype
Show answer and explanation
Heterozygous means the two alleles differ, so is heterozygous.
Question 2
In an incomplete-dominance example, red and white alleles produce pink heterozygotes. What pattern does pink represent?
- Complete dominance
- Codominance
- Incomplete dominance
- Multiple alleles
Show answer and explanation
Incomplete dominance
Pink is intermediate between red and white, which is the described incomplete-dominance pattern.
Question 3
A cross predicts a one-quarter chance of a recessive phenotype. What can you conclude about one offspring?
- It will certainly have the recessive phenotype.
- It cannot have the recessive phenotype.
- The model gives a probability, not certainty for that individual.
- Every group of four offspring must include exactly one with the phenotype.
Show answer and explanation
The model gives a probability, not certainty for that individual.
The fraction describes a chance across possible outcomes. It does not guarantee an individual result or an exact count in a small group.
Key terms
- Allele
- One version of a gene.
- Genotype
- The allele combination an organism has for a gene.
- Phenotype
- An observable form of a trait.
- Dominant allele
- An allele that determines the heterozygous phenotype in a complete-dominance model.
- Recessive allele
- An allele whose phenotype is masked by a dominant allele in a heterozygote in a complete-dominance model.
- Homozygous
- Having two matching alleles for a gene.
- Heterozygous
- Having two different alleles for a gene.
- Punnett square
- A grid used to list possible allele combinations in offspring.
Continue through SBI3U
View the complete SBI3U Ontario Grade 11 Biology curriculum and lessons
- D3.2 · Relate DNA, genes, chromosomes, alleles, mitosis, and meiosis
- D3.4 · Describe genetic disorders involving mutations or chromosome errors
- D1.1 · Analyse social and ethical implications of genetics research
- D1.2 · Evaluate recent advances in genetics knowledge and technology
- D2.1 · Use chromosome, allele, gamete, haploid, and diploid terminology
- D2.2 · Investigate meiosis and explain it with labelled diagrams
About this lesson and its review
Published by DoAssignment. This reviewed lesson follows Ontario Grade 11 Biology (SBI3U), expectation D3.3. It is a study resource, not an official curriculum publication.
Before publication, content is checked for structure, mathematical or chemical notation, calculations, course boundaries, and readability. Errors can still occur, so corrections are welcomed.