Core inheritance pattern
Inheritance in sexual life cycles occurs by production of haploid gametes and fusion at fertilization to form a diploid zygote.
A diploid organism has two alleles for each autosomal gene.
Always link inheritance to meiosis, random fusion of gametes, and allele combinations in offspring.
In exam answers, distinguish clearly between gene, allele, genotype, and phenotype.
Genetic crosses in flowering plants
Use P generation, F1 generation, F2 generation, and Punnett grid correctly.
In flowering plants, pollen carries the male gametes and ovules in the ovary contain the female gametes.
Pollination is required before fertilization can occur.
Some plants such as peas can self-pollinate and self-fertilize, making them useful in inheritance studies.
Genetic crosses are used in breeding crop varieties and ornamental plants.
Genotype and phenotype
Genotype = the combination of alleles inherited by an organism.
Phenotype = the observable traits of an organism, produced by genotype, environment, or both together.
Homozygous = two identical alleles.
Heterozygous = two different alleles.
Be ready to classify traits as:
genotype only
environment only
genotype × environment interaction
Dominant and recessive alleles
A dominant allele is expressed in the heterozygous condition.
A recessive allele is expressed only in the homozygous recessive condition.
This is why AA and Aa can have the same phenotype.
In monohybrid crosses, keep genotype ratios separate from phenotype ratios.
Do not say a dominant allele is “stronger”; say it is expressed in the heterozygote.
Phenotypic plasticity
Phenotypic plasticity = ability of an organism to develop traits suited to the environment experienced by changing patterns of gene expression.
Plasticity is not caused by a change in genotype.
Changes may be reversible during an individual’s lifetime.
High-scoring exam point: plasticity shows that phenotype is not determined by genotype alone.
Recessive disorders: PKU
Phenylketonuria (PKU) is a recessive genetic disorder caused by mutation in an autosomal gene.
The gene codes for the enzyme needed to convert phenylalanine to tyrosine.
An affected person must inherit two recessive alleles.
Unaffected carriers are heterozygous.
In pedigree or cross questions, identify PKU as autosomal recessive.
Multiple alleles and SNPs
A single-nucleotide polymorphism (SNP) is a variation at one base in the DNA sequence.
A gene pool can contain multiple alleles of a gene.
An individual organism still inherits only two alleles for that gene.
Exam distinction:
multiple alleles = many forms of a gene in a population
diploid individual = only two alleles present
ABO blood groups
ABO blood groups are an example of multiple alleles.
Use allele notation exactly: I^A, I^B, and i.
I^A and I^B are codominant.
i is recessive.
Genotypes and phenotypes:
I^A I^A or I^A i → blood group A
I^B I^B or I^B i → blood group B
I^A I^B → blood group AB
ii → blood group O

This image shows the relationship between ABO genotypes and phenotypes, including the role of I^A, I^B, and i. It is useful for checking codominance and multiple-allele inheritance at a glance. Source
Incomplete dominance vs codominance
Codominance: both alleles are fully expressed in the heterozygote.
Example: I^A I^B gives AB blood group with a dual phenotype.
Incomplete dominance: the heterozygote has an intermediate phenotype.
Example: four o’clock flower / marvel of Peru (Mirabilis jalapa).
Exam tip: do not confuse intermediate with both shown together.
Sex determination and sex linkage
In humans, the sex chromosome in the sperm determines whether the zygote develops male-typical or female-typical physical characteristics.
Eggs always carry X; sperm carry X or Y.
The X chromosome carries many more genes than the Y chromosome.
This is why sex-linked inheritance is usually discussed as X-linked inheritance.
Males are more likely to express X-linked recessive alleles because they have only one X chromosome.
Haemophilia as a sex-linked disorder
Haemophilia is a classic X-linked recessive disorder.
Write alleles as superscripts on X: for example X^H and X^h.
Male genotypes:
X^H Y = unaffected
X^h Y = affected
Female genotypes:
X^H X^H = unaffected
X^H X^h = carrier
X^h X^h = affected
Exam tip: a male cannot be a carrier for an X-linked recessive trait; he is either affected or unaffected.

This image shows inheritance patterns for an X-linked recessive trait, including outcomes when the mother is a carrier or the father is affected. It helps students predict why males are more often affected and how carrier daughters arise. Source
Pedigree charts
Pedigree charts are used to deduce patterns of inheritance of genetic disorders.
Standard symbols:
square = male
circle = female
shaded = affected
half-shaded = carrier (when shown)
Key clues:
autosomal recessive often appears in children of unaffected parents
autosomal dominant often appears in every generation
X-linked recessive affects more males and often shows no father-to-son transmission
Be able to infer possible genotypes from the pedigree.
The syllabus also expects awareness that marriage between close relatives increases the chance of homozygous recessive offspring.

This image shows how a pedigree chart can reveal an autosomal recessive inheritance pattern. It is especially helpful for practising how unaffected parents can produce affected offspring and how to infer carrier genotypes. Source
Continuous vs discrete variation
Continuous variation shows a range of phenotypes with no clear categories.
Discrete variation falls into distinct categories.
Skin colour in humans is an example of continuous variation caused by polygenic inheritance and/or environmental factors.
ABO blood group is an example of discrete variation.
Exam tip: continuous variation is usually influenced by many genes and often by the environment as well.
Polygenic inheritance
Polygenic inheritance occurs when a trait is controlled by multiple genes.
This usually produces continuous variation.
Environmental factors can further widen the range of phenotypes.
Good exam phrasing: continuous variation is due to polygenic inheritance and/or environmental effects.
Avoid oversimplifying skin colour as controlled by a single gene.
Data skills: mean, median, mode
For continuous data, be able to apply mean, median, and mode.
Mean = arithmetic average.
Median = middle value when data are ordered.
Mode = most frequent value.
Choose measures carefully:
median is often more useful when outliers are present
mode is useful for most common value
Box-and-whisker plots
A box-and-whisker plot displays six aspects of data:
outliers
minimum
first quartile (Q1)
median
third quartile (Q3)
maximum
Interquartile range (IQR) = Q3 − Q1.
A data point is an outlier if it is more than 1.5 × IQR above Q3 or below Q1 − 1.5 × IQR.
Use box plots for continuous variables such as student height.
In comparisons, look at median, spread, overlap, and outliers.

This image labels the main parts of a box-and-whisker plot, including the median, quartiles, and whiskers. It is ideal for revising exactly what each feature represents in IB data-analysis questions. Source
HL only: segregation and independent assortment
In meiosis, segregation means the two alleles of a gene separate so each gamete gets one allele.
Independent assortment applies to unlinked genes.
Unlinked genes are on different chromosomes or far enough apart to behave independently.
The movement of homologous chromosomes in meiosis I explains dihybrid ratios.
Always connect these ideas to random orientation of homologous pairs at metaphase I.
HL only: dihybrid crosses
Use Punnett grids to predict genotypic and phenotypic ratios in dihybrid crosses.
For AaBb × AaBb with unlinked autosomal genes, expected phenotype ratio is 9:3:3:1.
For AaBb × aabb (a test cross), expected phenotype ratio is 1:1:1:1 if genes are unlinked.
Build gametes correctly: AB, Ab, aB, ab.
Common error: forgetting that each gamete gets one allele from each gene.

This image shows the stages of meiosis leading to four haploid cells, which helps explain segregation and independent assortment. It is useful when linking chromosome behaviour in meiosis to expected outcomes in inheritance questions. Source
HL only: loci, linkage, and recombinants
A locus is the position of a gene on a chromosome.
Genes close together on the same chromosome are linked genes.
Linked genes do not assort independently as often as unlinked genes.
In linkage questions, show alleles beside vertical chromosome lines.
A recombinant has a new allele combination produced by crossing over.
In a cross between an individual heterozygous for both genes and an individual homozygous recessive for both genes, compare parental types with recombinant types.
For unlinked genes, recombinant and parental classes occur in equal proportions in a test cross.
For linked genes, parental combinations are usually more common than recombinants.
Checklist: can you do this?
Use Punnett grids for monohybrid and dihybrid crosses and give both genotype and phenotype ratios.
Distinguish dominance, codominance, incomplete dominance, multiple alleles, polygenic inheritance, and sex linkage.
Interpret pedigree charts to identify whether inheritance is autosomal dominant, autosomal recessive, or X-linked recessive.
Classify variation as continuous or discrete and explain the role of genes and the environment.
Read and construct box-and-whisker plots, including IQR and outlier identification.
Exam traps to avoid
Do not confuse genotype with phenotype.
Do not say codominance and incomplete dominance are the same.
Do not forget that multiple alleles exist in a population, not all in one individual.
Do not say males are “heterozygous” for X-linked genes; they are hemizygous because they have only one X chromosome.
Do not assume every continuous trait is purely genetic; the syllabus allows polygenic inheritance and/or environmental factors.
In pedigrees, do not miss the clue that close relatives are more likely to share the same recessive allele.
Fast-recall summary
Dominant: expressed in heterozygotes.
Recessive: expressed only in homozygotes.
Codominance: both alleles fully expressed.
Incomplete dominance: heterozygote is intermediate.
Multiple alleles: more than two alleles in population.
Sex-linked: gene on a sex chromosome, usually X-linked.
Polygenic: many genes affect one trait.
Linked genes: genes on same chromosome, so independent assortment may fail.
Recombinants: new combinations caused by crossing over.

Shubhi is a seasoned educational specialist with a sharp focus on IB, A-level, GCSE, AP, and MCAT sciences. With 6+ years of expertise, she excels in advanced curriculum guidance and creating precise educational resources, ensuring expert instruction and deep student comprehension of complex science concepts.
Shubhi is a seasoned educational specialist with a sharp focus on IB, A-level, GCSE, AP, and MCAT sciences. With 6+ years of expertise, she excels in advanced curriculum guidance and creating precise educational resources, ensuring expert instruction and deep student comprehension of complex science concepts.