LZHS H Bio I Topic 8 Inheritance of Traits

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Last updated 3:31 AM on 3/12/25
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22 Terms

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Chromosome

A threadlike, gene-carrying structure found in the nucleus. Each chromosome consists of one very long DNA molecule and associated proteins.

<p>A threadlike, gene-carrying structure found in the nucleus. Each chromosome consists of one very long DNA molecule and associated proteins.</p>
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Somatic Cells

any cell of a living organism other than the reproductive cells, diploid (2n)

<p>any cell of a living organism other than the reproductive cells, diploid (2n)</p>
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Gametes

a mature haploid (n) male or female germ cell that is able to unite with another of the opposite sex in sexual reproduction to form a zygote.

<p>a mature haploid (n) male or female germ cell that is able to unite with another of the opposite sex in sexual reproduction to form a zygote.</p>
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Independent Assortment

the random distribution of the pairs of genes on different chromosomes to the gametes

<p>the random distribution of the pairs of genes on different chromosomes to the gametes</p>
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Meiosis

a type of cell division that results in four daughter cells each with half the number of chromosomes of the parent cell, as in the production of gametes.

<p>a type of cell division that results in four daughter cells each with half the number of chromosomes of the parent cell, as in the production of gametes.</p>
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Pedigree

A diagram that shows the occurrence of a genetic trait in several generations of a family.

<p>A diagram that shows the occurrence of a genetic trait in several generations of a family.</p>
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Karyotype

A display of the chromosome pairs of a cell arranged by size and shape.

<p>A display of the chromosome pairs of a cell arranged by size and shape.</p>
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XX Chromosomes

female sex chromosomes

<p>female sex chromosomes</p>
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XY Chromosomes

male sex chromosomes

<p>male sex chromosomes</p>
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Mutation

A change in a gene or chromosome.

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Deletion

removes a chromosomal segment

<p>removes a chromosomal segment</p>
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Insertion

A mutation involving the addition of one or more nucleotide pairs to a gene.

<p>A mutation involving the addition of one or more nucleotide pairs to a gene.</p>
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Substitution

A mutation in which a nucleotide or a codon in DNA is replaced with a different nucleotide

<p>A mutation in which a nucleotide or a codon in DNA is replaced with a different nucleotide</p>
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Germ Mutation

mutation or mistake in a germ or reproductive cell, can be passed to offspring

<p>mutation or mistake in a germ or reproductive cell, can be passed to offspring</p>
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Somatic Cell Mutation

change within cells of the body, cannot be transmitted

<p>change within cells of the body, cannot be transmitted</p>
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Environmental Mutations

damage to DNA and chromosomes caused by environmental factors

<p>damage to DNA and chromosomes caused by environmental factors</p>
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Environmental Factors

Those "nonbiological" factors that are involved in a person's surroundings such as the nature of the person's parents, the person's friends, and the person's behavioral choices.

<p>Those "nonbiological" factors that are involved in a person's surroundings such as the nature of the person's parents, the person's friends, and the person's behavioral choices.</p>
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Pollutant

A material found in air, water, or soil that is harmful to humans or other organisms, can cause an environmental mutation

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Crossing Over

exchange of genetic material between homologous chromosomes during prophase I of meiosis

<p>exchange of genetic material between homologous chromosomes during prophase I of meiosis</p>
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Genetic Variation in Meiosis

Results in cells that are genetically different as the result of crossing over and independent assortment

<p>Results in cells that are genetically different as the result of crossing over and independent assortment</p>
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Nondisjunction in Meiosis I

Homologous chromosomes do not separate properly (all cells abnormal); usually occurs during Anaphase 1

<p>Homologous chromosomes do not separate properly (all cells abnormal); usually occurs during Anaphase 1</p>
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Trisomy

3 copies of a chromosome; occurs when chromosomes fail to separate properly

<p>3 copies of a chromosome; occurs when chromosomes fail to separate properly</p>