Year 10 - Science
Alleles, genotype, and phenotype
Inheritance, genotype and phenotype
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This pupil-friendly study guide includes a unit summary, clear notes, common mistakes, and quick questions with answers.
Year 10 - Science
Inheritance, genotype and phenotype
This unit covers key genetic terms, single-gene inheritance, and genetic crosses, including probability and ratios. It explores how most traits result from multiple genes and sex determination in humans. The unit also includes interpreting data and using models to solve problems.
You will learn to explain how the genotype affects the phenotype of an organism.
An individual inherits two copies of each gene in a pair of chromosomes. Versions of genes are called alleles, they can be recessive or dominant, indicated with a capital or lowercase letter.
A genetic variant in a gene creates an allele (a different version of the gene), which produces a different phenotype. Include the word in a full scientific explanation, not as a single label.
Mistake: A dominant condition is 'stronger' and that only the strongest characteristic is inherited from one parent. Correction: Two genes are inherited, so both alleles contribute to the genotype. In some cases one is dominant and therefore will always be expressed (through protein structure) in the phenotype, the recessive allele is still present.
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