Deoxyribonucleic acid, the chemical that all of our genetic material is made of
DNA
It's a polymer made up of lots of similar units stuck together
It has two strands which are stuck together to form a double helix
If you unraveled all the DNA in a single cell, the strand would be over two meters long</b>
Chromosome
A really tight coil of DNA, there are 46 chromosomes in each of our cells
There are only 23 different types of chromosomes, as we have two of each type, one from each parent
Sex chromosomes
The 23rd pair of chromosomes, women have two X chromosomes, men have one X and one Y
Chromosomes only look like an X shape just before cell division, usually they look more like a single coil
Gene
A small section of DNA that codes for a particular type of protein
There are only 20 different types of amino acids, but they can be combined in many different sequences to form thousands of different proteins
Genome
The entire set of genetic material in an organism
Scientists have now worked out the complete human genome, the entire code that our DNA holds
Genes can either cause a particular disease (inherited disease) or just increase the risk of a disease
Genomes can be used to trace the migrations of our ancestors by looking at small differences between populations
DNA (deoxyribonucleic acid) is the molecule that contains all the genetic information needed to build and maintain living organisms.
DNA (deoxyribonucleic acid) is the molecule that carries genetic information from one generation to the next.
Genes are segments of DNA that contain information about specific traits or characteristics, such as eye color or height.
The human genome is the complete set of genetic instructions that make up an individual.
A gene is a section of DNA that codes for a specific protein or RNA molecule.
Protein synthesis involves two main stages: transcription and translation
A gene is a section of DNA that codes for a specific protein
A chromosome is a long strand of DNA that contains many genes.
A gene mutation occurs when there is a change in the sequence of nucleotides within a gene, which can alter its function or expression.
An allele is a variant form of a gene.
Transcription occurs inside the nucleus where RNA polymerase reads the base sequence on one strand of DNA and makes a complementary copy using free ribonucleotides
The Human Genome Project was an international effort to sequence the entire human genome and identify all its genes.
A gene is a segment of DNA that codes for a protein or RNA molecule.
Mutations can occur spontaneously due to errors during cell division or exposure to environmental factors like radiation or chemicals.
Chromosomes are structures within cells that carry genes and other genetic material.
The structure of DNA consists of two strands twisted together into a double helix shape.
Some mutations may have no effect on health, while others can lead to inherited diseases or cancer.
Gene expression refers to the process by which genes are turned on or off to control cellular functions
During cell division, the chromosomes replicate to ensure that each new cell receives a full copy of the genetic material.
Ribosomes are cellular structures where proteins are synthesized using the information encoded in DNA.
Chromosomal abnormalities occur when there are changes to the number or structure of chromosomes, such as deletions, duplications, or rearrangements.
Chromosomal abnormalities occur when there are changes to the number or structure of chromosomes, such as deletions, duplications, or rearrangements.
Mutations can occur spontaneously due to errors during replication or exposure to mutagens like radiation or chemicals.
Chromosomes can be identified by their size and shape under a microscope.
The genotype refers to an individual's complete set of genetic information, while the phenotype describes their observable traits.
Transcription is the process by which a segment of DNA is copied into mRNA
Each organism has a unique number of chromosomes, which determines its species.