S5 Biology: Mendelian Genetics (Paper 3)
- 2026-11-01
S5 Biology: Mendelian Genetics (Paper 3)
The third paper works through real cases: reading recessive pedigrees, codominance and multiple alleles in ABO blood groups, X-linked colour blindness, and using the two thirds carrier chance to estimate the next generation risk.
Direct answer Unaffected parents with an affected child means recessive inheritance; ABO has three alleles with IA and IB codominant; a son takes his X from his mother, so half his risk follows her carrier state; risk multiplies carrier chances by one quarter.
01 Paper details (check answers afterwards)
| Item | Detail |
|---|---|
| Questions | 10 |
| Suggested time | 25 |
| Difficulty mix | Foundation 3 · Intermediate 3 · Challenge 3 · Error redo 1 |
| Chapter | Chapter: S5 Biology: Mendelian Genetics |
| Level | Four basic, three advanced, two challenge and one error-repair item |
02 Questions (10 items)
- FoundationTwo unaffected parents have a child with albinism. What does that tell you about the allele?
- FoundationTwo Aa parents have a child. What is the chance the child is affected?
- FoundationWhat is the genotype of blood group AB?
- IntermediateHow many alleles control the ABO blood groups?
- IntermediateOne parent is AB and the other O. What blood groups can the children have?
- IntermediateAmong the normal children of two Aa carriers, what fraction are themselves carriers?
- ChallengeColour blindness is X-linked recessive. With a XCXc mother and a XCY father, what is the chance a son is colour blind?
- ChallengeIf that couple had 200 sons, how many would be expected to be colour blind?
- ChallengeTwo relatives each have a two in three chance of being carriers. What is the risk that their child is affected?
- Error redoA student says a dominant disorder can skip a generation. What is wrong?
03 Answers and one-line notes
| # | Answer | One-line note |
|---|---|---|
| 1 | It is recessive | A recessive trait can hide in heterozygous parents and only appears when both pass the allele on. |
| 2 | One quarter | Only aa is affected, one square of the four in the grid. |
| 3 | IAIB, with both alleles expressed, which is codominance | Neither IA nor IB masks the other, so the red cells carry both A and B antigens. |
| 4 | Three: IA, IB and i | Only two of the three are carried at a time, giving six genotypes and four blood groups. |
| 5 | A or B, half each; never AB or O | IAIB passes only IA or IB while O passes only i, so children are IAi or IBi. |
| 6 | Two thirds | Normal children cover one AA and two Aa, so two thirds are carriers, the figure used for the next generation. |
| 7 | One half | A son always takes his X from his mother, and one of her two X chromosomes carries the allele, so the chance is one half. |
| 8 | About 100 | Two hundred times one half gives 100, and real counts will come close without matching exactly. |
| 9 | One ninth | Two thirds times two thirds times one quarter gives four thirty-sixths, that is one ninth. |
| 10 | A dominant disorder appears in every generation; skipping is a feature of recessive inheritance | A dominant condition always has an affected parent, so a skipped generation means the allele is not dominant. |
04 What to do after marking
- After marking, redo only the wrong items and write down which step went wrong (formula, unit, or misread number).
- Repeat the same item two days later; move to the next paper only when both attempts are correct.
- Parents only need the answer and note columns; there is no need to explain every item.
Book an S5 Biology tutorTutor Registration →
Questions and answers are written originally by the TutorZone team and are not taken from any school, publisher or examination authority paper. Every value is checked by computer.


