Genetics Notes Review

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This set of flashcards covers key genetic terms and definitions based on the lecture notes on foundational genetics concepts.

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36 Terms

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Gregor Mendel

Founder of modern genetics who studied the inheritance of traits in pea plants.

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Allele

A version of a gene that can cause different traits, such as yellow or green peas.

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Homozygous

Having two identical alleles for a particular gene.

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Heterozygous

Having two different alleles for a particular gene.

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Dominant allele

An allele that is expressed when two different alleles are present.

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Recessive allele

An allele that is expressed only when two copies are present.

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Gene

A section of DNA that provides instructions for making proteins.

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Trait

A physical or behavioral characteristic influenced by genes.

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Law of Segregation

During gamete formation, allele pairs separate so that a sperm or egg carries only one allele for each trait.

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Punnett Square

A diagram that shows the possible genotypes of offspring from a genetic cross.

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Dihybrid Cross

A genetic cross that examines two traits at once, resulting in a 9:3:3:1 phenotypic ratio.

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Monohybrid Cross

A genetic cross that examines the inheritance of a single trait.

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Test Cross

A method to determine the genotype of an organism exhibiting a dominant trait by crossing it with a homozygous recessive.

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Probability

The likelihood that an event will occur, used in genetics to predict inheritance outcomes.

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Independent assortment

The principle stating that allele pairs segregate independently during gamete formation.

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Chromatin

Loose, messy DNA in the nucleus, existing when the cell isn’t dividing.

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Chromosome

Neatly packed DNA that forms thick, X-shaped structures before cell division.

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Sister chromatids

Identical halves of a duplicated chromosome, connected in the middle.

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Homologous chromosomes

A pair of chromosomes that are the same size and shape, containing the same types of genes.

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Genotype

The genetic constitution of an organism, represented by letters (e.g., YY, Yy, yy).

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Phenotype

The observable physical traits of an organism, influenced by genotype.

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Non-Mendelian Genetics

Patterns of inheritance that do not follow Mendel's simple rules of dominant and recessive traits.

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Incomplete Dominance

Neither allele is fully dominant; traits blend together.

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Codominance

Both alleles are equally expressed in the phenotype.

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Genetic Linkage

Genes that are located on the same chromosome and tend to be inherited together.

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Multiple Alleles

More than two allele options for a gene, such as the ABO blood group.

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Polygenic Inheritance

Many genes control one trait, leading to a range of phenotypes.

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Sex-Linked Traits

Traits that are associated with genes located on the sex chromosomes, typically on the X chromosomes.

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Crossing Over

The exchange of segments of DNA between homologous chromosomes during meiosis, contributing to genetic variation.

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Crossover Frequencies

The frequency at which crossover events happen, measured in percentages to create genetic maps.

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Nondisjunction

The failure of chromosomes to separate properly during meiosis, leading to disorders like trisomy and monosomy.

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Trisomy 21

A condition where an individual has three copies of chromosome 21, also known as Down's Syndrome.

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Klinefelter's Syndrome

A genetic condition in males characterized by one extra X chromosome (XXY).

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Turner's Syndrome

A genetic condition in females where one of the X chromosomes is missing or partially missing (X0).

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Karyotype

A laboratory technique that produces an image of an individual's complete set of chromosomes, used to identify chromosomal abnormalities.

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X chromosome inactivation

The process by which one of the two X chromosomes in females is randomly silenced, preventing the dosage imbalance of X-linked genes.