Sure! Here are definitions for each of the terms:
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Gene: A gene is a specific sequence of DNA that contains the instructions for building a particular protein or set of proteins. Genes are the basic units of heredity and are responsible for the traits and characteristics of an organism. Each gene occupies a specific location on a chromosome and can vary in sequences among individuals, leading to different traits.
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Chromosome: A chromosome is a long, thread-like structure composed of DNA and proteins that carries genetic information. In humans and many other organisms, chromosomes are found in pairs; humans typically have 23 pairs (46 chromosomes in total). Each chromosome contains many genes, and the specific arrangement of these genes along a chromosome can influence an organism's characteristics.
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Genotype: The genotype refers to the genetic makeup of an organism, specifically the alleles (versions of a gene) that an organism has for a particular trait. It is usually expressed in terms of the combinations of alleles inherited from the parents (e.g., homozygous dominant, heterozygous, homozygous recessive). The genotype provides the genetic potential for the organism but does not always determine the observable traits.
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Phenotype: The phenotype is the observable physical, biochemical, or behavioral characteristics of an organism, resulting from the interaction between its genotype and the environment. Examples of phenotypic traits include eye color, height, and behavior. While the phenotype is influenced by the genotype, environmental factors can also have a significant impact on the final expression of traits.
In summary, the genotype is the genetic blueprint of an organism, while the phenotype is the manifestation of that genetic information in conjunction with environmental influences. Genes are parts of chromosomes that carry genetic instructions.