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Genetic Units

Science :)

QuestionAnswer
Heredity Heredity: The passing of physical or mental characteristics (traits) from parents to offspring.
Sex chromosomes Sex chromosomes: The pair of chromosomes that determine if an organism is male (XY) or female (XX).
Trait Trait: A specific characteristic or feature of an organism, such as eye color or height
Sex-linked gene Sex-linked gene: A gene located on a sex chromosome (usually the X), which means the trait is inherited differently depending on sex.
Genetics Genetics: The scientific study of heredity and how traits are passed down.
Carrier Carrier: A person who has one recessive gene for a disease but does not show symptoms, yet can pass it on.
Genetic disorder Genetic disorder: A health problem caused by a defect or mutation in a person's DNA.
Purebred Purebred: An organism that always produces offspring with the same traits, having two identical genes for a trait (homozygous).
Pedigree Pedigree: A diagram or family tree that tracks the inheritance of a specific trait over several generations.
Karyotype Karyotype: A picture of all the chromosomes in a cell, arranged in pairs to check for abnormalities.
Allele Allele: A different form or version of a gene (e.g., blue eye allele vs. brown eye allele).
Selective breeding Selective breeding: The process of humans breeding plants or animals to choose specific desirable traits.
Dominant allele Dominant allele: A version of a gene that shows its trait even if only one copy is present (masks recessive).
Inbreeding Inbreeding: The mating of closely related individuals, which increases the chance of inheriting similar genes.
Recessive allele Recessive allele: A version of a gene that only shows its trait if two copies are present (hidden by dominant).
Hybridization Hybridization: The crossing of two different types of plants or animals to create a mix of traits.
Hybrid Hybrid: The offspring produced by breeding two different varieties (heterozygous)
Clone Clone: An organism that is genetically identical to its parent.
Punnett square Punnett square: A grid diagram used to predict the possible genetic outcomes (traits) of offspring.
Genetic engineering Genetic engineering: Directly manipulating an organism’s genes using technology to change its traits.
Phenotype Phenotype: The physical appearance or observable traits of an organism.
Gene therepy Gene therapy: An experimental technique that fixes or replaces faulty genes to treat disease.
Genotype Genotype: The specific combination of alleles (genetic code) an organism has.
Genome Genome: The complete set of genetic material (all DNA) in an organism.
Homozygous Homozygous: Having two identical alleles for a particular gene (e.g., AA or aa).
Ethics Ethics: The branch of knowledge dealing with moral principles, particularly regarding the use of genetics.
Heterozygous Heterozygous: Having two different alleles for a particular gene (e.g., Aa).
Meiosis Meiosis: The cell division process that creates sex cells (sperm/eggs) with half the number of chromosomes.
Incomplete dominance Incomplete dominance: A situation where neither allele is fully dominant, resulting in a blended phenotype (e.g., red+white=pink).
Crossing Over Crossing Over: The exchange of genetic material between chromosomes during meiosis, creating variation.
Codominance Codominance: A situation where both alleles are expressed equally and at the same time (e.g., red+white=spots).
Zygote Zygote: The cell formed by the union of two gametes (a fertilized egg)
Multiple alleles Multiple alleles: A gene that has more than two possible allele options (e.g., blood types A, B, O).
Gametes Gametes: Reproductive cells (sperm or egg) that carry only one set of chromosomes.
Polygenic inheritance Polygenic inheritance: A trait controlled by two or more genes, leading to a range of options (e.g., skin color).
Protein Synthesis Protein Synthesis: The process cells use to create proteins based on instructions from DNA.
Messenger RNA Messenger RNA (mRNA): A molecule that carries instructions from DNA in the nucleus to the rest of the cell.
Autosomal Chromosomes Autosomal Chromosomes: All chromosomes that are not sex chromosomes (humans have 22 pairs).
Transfer RNA Transfer RNA (tRNA): A molecule that helps decode mRNA and brings the correct amino acids to build proteins.
Mutation Mutation: A permanent, random change in the DNA sequence.
Fertilization Fertilization: The process where a male gamete (sperm) and female gamete (egg) join to create a new cell.
Gene Gene: A small section of DNA on a chromosome that contains instructions for a specific trait.
Created by: KingNugz
 

 



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