A sequence of nucleotides, that is part of a DNA molecule, controls the production of one particular polypeptide. It is also a unit of inheritance.
Allele
Different forms of the same gene. Alleles occupy the same locus on a pair of homologous chromosomes.
One chromosome is from father and another is from mother, if they have the exact same genes, they are homologous chromosomes.
Alleles of "eyelid type" gene
Single eyelid - AAA AAA AAA
Double eyelid - AAA TAA AAA
Genotype
The combination of alleles for a particular gene.
Phenotype
The expressed trait or outward appearance.
Homozygous
Having the two identical alleles of a particular gene.
Heterozygous
Having two different alleles of a particular gene.
Dominant allele
Expresses itself and gives the same phenotype in both homozygous dominant and heterozygous conditions.
Recessive allele
Only expresses itself in homozygous recessive condition.
Genetic diagram
A model used to explain how alleles are passed on to an offspring and predict the phenotype that will be displayed by an offspring.
Punnett square
A genetic model used to predict the phenotype that will be displayed by an offspring.
Ratio = 3 tall : 1 dwarf NOT 3:1. Chance = 75% tall and 25% dwarf!
Genetic diagram for PKU cross between homozygous dominant and homozygous recessive parents
N/N x n/n
Punnett square for PKU cross between homozygous dominant and homozygous recessive parents
N/N x n/n
Genetic diagram for PKU cross between two heterozygous parents
N/n x N/n
Punnett square for PKU cross between two heterozygous parents
N/n x N/n
Observed ratios different from expected ratios
Reason: 1. The sample size is too small. 2. Fertilisation is a random process.
Codominance
When two alleles controlling a trait both express themselves in the organism.
Multiple alleles
Gene that exists in more than two alleles.
Sex chromosomes
X and Y chromosomes.
Sex determination genetic diagram
Male gametes contain X or Y, female gametes contain X
Mutation
The sudden random change in the sequence of a gene or chromosome number.
Sickle-cell anaemia
Caused by a gene mutation that results in haemoglobin S instead of normal haemoglobin A. This makes red blood cells sickle-shaped and have lower oxygen carrying capacity.
Albinism
Caused by a gene mutation that results in loss of pigments in skin, hair and eyes. Sensitive to sunlight.
Down syndrome
Caused by an extra copy of chromosome 21. Results in characteristic facial features and mental/physical difficulties.
Continuous variation
Traits that show a range that can be expressed in infinite decimal places.
Discontinuous variation
Traits that show clear and distinct traits that is either a "yes" or "no".
Continuous variation is affected by many genes, discontinuous variation is affected by 1 or few genes.
Continuous variation
Height, skin colour, weight, intelligence
Discontinuous variation
Eye-lid types, ability to roll tongue, blood group