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genetic unit vocab
| Term | Definition |
|---|---|
| Heredity | The passing of traits or physical characteristics from parents to their offspring. |
| Trait | A specific, observable, or measurable characteristic or quality of an organism, such as hair color or eye color. |
| Genetics | The scientific study of heredity and the variations in living organisms, focusing on how traits are passed down. |
| Fertilization | The process in which male and female gametes (sperm and egg) fuse to create a new, unique organism. |
| Purebred | An organism that is the offspring of genetically similar parents, often produced through inbreeding to ensure consistent traits (homozygous). |
| Gene | A discrete unit of hereditary information, typically a segment of DNA that determines a particular trait. |
| Allele | One of the different versions or forms of a gene, occupying a specific position on a chromosome. |
| Dominant allele | An allele whose trait always shows up in the organism when it is present, masking the effect of a recessive allele. |
| Recessive allele | An allele that is only expressed when an organism inherits two copies of it (one from each parent); it is masked by a dominant allele. |
| Hybrid | An organism that has two different alleles for a trait (heterozygous |
| Punnett square | A diagram used by geneticists to calculate the probabilities of potential genotypes in offspring. |
| Phenotype | The observable physical or biochemical characteristics of an organism, determined by both genetic makeup and environmental influences. |
| Genotype | The specific set of alleles (genetic makeup) for a given organism. |
| Homozygous | Having two identical alleles for a specific trait |
| Heterozygous | Having two different alleles for a specific trait |
| Incomplete dominance | A form of inheritance where one allele is not completely dominant over the other, resulting in a blended or intermediate phenotype |
| Codominanc | A condition in which both alleles for a gene are expressed equally and simultaneously in the phenotype |
| Multiple alleles | A gene that has more than two possible alleles (e.g., blood type, which has A, B, and O). |
| Polygenic inheritance | A trait controlled by more than one gene, often resulting in a continuous range of phenotypes |
| Messenger RNA | RNA molecule that carries copies of instructions for assembling amino acids into proteins from DNA to the rest of the cell. |
| Transfer RNA | Type of RNA molecule that transfers amino acids to ribosomes during protein synthesis. |
| Mutation | A permanent alteration in the DNA sequence that makes up a gene, which can lead to new traits or variations. |
| Sex chromosomes | Chromosomes that determine the sex of an organism (in humans, X and Y). |
| Sex-linked gene | A gene located on a sex chromosome (usually the X chromosome), causing different inheritance patterns in males and females. |
| Carrier | A person who has one recessive allele for a genetic disorder but does not show the symptoms, yet can pass it on. |
| Genetic disorde | A disease or condition caused by an abnormality in an individual's DNA, such as a mutation or incorrect number of chromosomes. |
| Pedigree | A diagram that shows the occurrence and appearance of phenotypes of a particular gene or organism and its ancestors from one generation to the next |
| Karyotype | A picture of all the chromosomes in a cell, arranged in pairs to check for abnormalities. |
| Selective breedin | The process of selecting organisms with desired traits to serve as parents for the next generation. |
| Inbreeding | The mating of closely related individuals, often used to maintain specific traits in a population. |
| Hybridization | The crossing of two different, but related, species or varieties to produce an offspring with characteristics of both. |
| Clone | n organism that is genetically identical to its parent |
| Genetic engineering | The deliberate modification of the characteristics of an organism by manipulating its genetic material |
| Gene therepy | A technique that modifies a person’s genes to treat or prevent disease. |
| Genome | The full set of genetic material (all DNA) present in a cell or organism. |
| Ethics | The study of moral principles, particularly regarding the use of technology in genetics. |
| Meiosis | A type of cell division that reduces the number of chromosomes in the parent cell by half to produce four gamete cells (sperm or egg). |
| Crossing Over | The exchange of genetic material between homologous chromosomes during meiosis, contributing to genetic variation. |
| Zygote | The fertilized egg cell that results from the union of a female gamete (egg) and a male gamete (sperm). |
| Gametes | Reproductive cells (sperm or egg) that carry half the genetic material of the parent organism (haploid). |
| Protein Synthesis | The process by which cells build proteins, using information coded in DNA. |
| Autosomal Chromosomes | Any chromosome that is not a sex chromosome (non-sex-linked chromosomes). |