A branch of Biology that deals with the study of genes, heredity and Variation in organisms
Charles Darwin and Wallace's views
1859
Mendel's work laid the foundation for the understanding of genetics
Chromosomes
Thread-like structures located in the nucleus of cells that carry genetic information in the form of genes
DNA
The chemical that carries the genetic instructions in the cells of organisms
DNA is a double helix structure
Heredity
The transmission of traits from parents to offspring
Variation
The ability of an organism to acquire traits or characters from its own parents
Phenotype
The physical or observable traits displayed by an organism
Genotype
The genetic makeup of an organism that produces the phenotype
Dominant traits
Traits that are expressed in the offspring when present
Recessive traits
Traits that are hidden or not expressed in the offspring when present
Homozygous
An individual with two similar genes that perform the same characters
Heterozygous
An individual with two different pairs of genes controlling different characters
Haploid
An organism with one set of chromosomes
Diploid
An organism with two sets of chromosomes
Mutation
A process whereby there is a slight alteration or change in the gene of an organism leading to the formation of new characteristics
Genetic linkage
The physical association of materials found on the same location, whereby genes can be inherited together due to their close association on a chromosome
Sex linkage
Traits that are associated with the sex chromosomes (X and Y)
Sex-linked abnormalities
Colour blindness
Haemophilia (bleeding disease)
Genetic linkage
The physical association of genes on the same location, whereby genes can be inherited together due to their close association - it can take place on a chromosome
Sex linkage
It takes place in the Sex Chromosome. The X chromosome is larger in size and carries more genes, it moves faster than the Y chromosome which is smaller in size and carries less genes
Abnormalities associated with sex linkage
Colour blindness
Haemophilia (Bleeding Disease)
Baldness
Sickle cell anaemia
An abnormality caused by recessive genes which cause the red blood cells of some organisms to become sickled shape
Albinism
A situation where the skin of an organism is non-pigmented (lacks melanin pigment)
Crossing over
A process that leads to exchange of genetic materials between chromosomes
Example of crossing over
Parent 1 x Parent 2 = Recombinant offspring
Genetic recombination
The combination or exchange of genetic materials during meiosis
Allele
Different forms of the same gene
Genetic population or population genetics
The study of genetic variation and evolutionary changes in a particular area or population of organisms
Genetic variation
The different genes that occur in a population
Gene pool
The sum of all the varieties of genes present in a population, which changes from generation to generation
Allele frequency
How often a form of a gene shows up/reoccurs in a population over several generations
Phenotypical variation
The visible differences in phenotypes that exist in a population
Random mating
A situation where each and every organism in an environment have equal right of mating with other organisms of the same type
Genetic diseases
Disorders caused genetically, which have no environmental remedy but can only be controlled
Mutation
An alteration of genes or chromosomes that can lead to the formation of new characteristics
Down Syndrome
A genetic disorder caused by the failure of the 21st chromosome to separate during egg or sperm formation, resulting in an extra copy of the 21st chromosome
Turner's Syndrome
A monosomic disorder in females where they have only one X chromosome instead of two
Klinefelter's Syndrome
A disorder in males where they have an extra X chromosome, resulting in physical and fertility issues