D3.2.5—Dominant and recessive alleles
Dominant alleles affect phenotype in heterozygotes, while recessive alleles are expressed only when no dominant allele is present in inheritance problems.
- Syllabus
- First assessment 2025
- Objective
- D3.2.5
- Level
- HL
Dominant alleles affect phenotype in heterozygotes, while recessive alleles are expressed only when no dominant allele is present in inheritance problems.

Coverage 2016–2022 · Updated 16 Jul 2026
Under complete dominance, a dominant allele determines the heterozygous phenotype. A recessive phenotype appears only when no dominant allele is present.
| Genotype | Allele state | Phenotype when T is dominant |
|---|---|---|
| TT | homozygous dominant | tall |
| Tt | heterozygous | tall |
| tt | homozygous recessive | dwarf |
Dominant does not mean better, stronger or more common. It only describes expression in a heterozygote; a harmful or rare allele can be dominant.
P generation: true-breeding tall TT × true-breeding dwarf tt → every gamete carries T or t, respectively.
F1 generation: every offspring is Tt and tall. The t allele has not blended away; its phenotypic effect is masked in the heterozygote.
F1 self-cross: Tt × Tt → F2 genotypes 1 TT : 2 Tt : 1 tt → phenotypes 3 tall : 1 dwarf in a large sample.
Reappearance of dwarf offspring shows that hereditary factors remain discrete across generations. The observed ratio approaches the probability prediction only when many offspring are counted.
| Tt × Tt | T gamete | t gamete |
|---|---|---|
| T gamete | TT, tall | Tt, tall |
| t gamete | Tt, tall | tt, dwarf |
Each cell has probability 1/4 because each parent produces T and t gametes with probability 1/2. The grid predicts probabilities for each fertilization, not a guarantee that every four offspring will contain one of each cell.
A tall plant could be TT or Tt because both contain the dominant T allele. Cross the unknown plant with a homozygous recessive tester, tt, whose gametes reveal what the unknown parent contributes.
| Unknown parent | Cross with tt | Expected offspring evidence |
|---|---|---|
| TT | TT × tt | all Tt, all tall |
| Tt | Tt × tt | about 1 Tt tall : 1 tt dwarf |
A small all-tall sample does not prove the parent is TT because a heterozygote can produce tall offspring repeatedly by chance. Confidence increases as more offspring are scored.
| Genotype | PKU status | Reproductive meaning |
|---|---|---|
| PP | unaffected, not a carrier | passes P |
| Pp | unaffected carrier | can pass P or p |
| pp | affected | passes p |
| Pp × Pp | P gamete | p gamete |
|---|---|---|
| P gamete | PP unaffected | Pp carrier |
| p gamete | Pp carrier | pp affected |
For each pregnancy: 1/4 affected, 1/2 unaffected carrier, 1/4 unaffected non-carrier. The probability resets for every fertilization; previous children do not change the next gamete combination.
Carrier and affected are not synonyms. A heterozygous carrier has a working dominant allele and usually does not show PKU, but can transmit the recessive allele.
| Allele relationship | Heterozygote phenotype | Example |
|---|---|---|
| complete dominance | matches the dominant homozygote | Tt pea is tall |
| codominance | both allele products are detectably expressed | IᴬIᴮ has A and B antigens |
| incomplete dominance | intermediate between the two homozygotes | red × white Mirabilis gives pink F1 |
| Heterozygote × heterozygote | Genotype ratio | Phenotype ratio |
|---|---|---|
| complete dominance | 1:2:1 | 3:1 |
| codominance or incomplete dominance | 1:2:1 | 1:2:1 when all three genotypes are distinguishable |
Codominance is not blending: both products remain identifiable. In incomplete dominance, the heterozygote is intermediate rather than showing two separate products side by side.
homologous chromosomes carry two alleles in a diploid parent → meiosis separates one allele into each gamete → fertilization restores a two-allele genotype → allele relationship and environment shape phenotype → offspring data test the prediction
For any genetic cross:
| If the simple 3:1 expectation fails | First question to ask |
|---|---|
| heterozygote has a third phenotype | incomplete dominance? |
| both products appear | codominance? |
| phenotype changes with conditions | environmental or plastic response? |
| more than two alleles occur in the population | multiple-allele locus such as ABO? |
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Many genetic diseases are due to recessive alleles of autosomal genes that code for an enzyme. Using a Punnett grid, explain how parents who do not show signs of such a disease can produce a child with the disease.