Unit 5: Hereditary

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Last updated 10:40 AM on 12/16/24
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33 Terms

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Gametes

Sex cells that are haploid and combine from two parents to form a diploid zygote.

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Haploid

A cell that contains one complete set of chromosomes.

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Diploid

A cell that contains two complete sets of chromosomes, one from each parent.

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Zygote

The fertilized egg that develops from the merging of two gametes.

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Gregor Mendel

The monk known as the Father of Genetics who discovered the principles of heredity.

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Locus

The specific position of a gene on a chromosome.

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Homologous chromosomes

Pairs of chromosomes that are the same size, shape, and carry the same genes, but may contain different alleles.

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Alleles

Different versions of a gene.

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Homozygous

An organism with two identical alleles for a particular trait.

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Heterozygous

An organism with two different alleles for a particular trait.

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Phenotype

The physical appearance of an organism as a result of its genotype.

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Genotype

The genetic makeup of an organism, comprising the alleles it possesses.

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Dominant allele

An allele that is expressed in the phenotype even in the presence of a recessive allele.

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Recessive allele

An allele that is only expressed in the phenotype if two copies are present.

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Punnett square

A diagram used to predict the genotype and phenotype combinations in genetic crosses.

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Law of Dominance

The principle stating that one trait can mask the effects of another trait.

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Law of Segregation

Each gamete gets only one copy of each gene, resulting in allele separation during gamete formation.

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Law of Independent Assortment

Genes for different traits are inherited independently of one another.

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Monohybrid cross

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

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Dihybrid cross

A genetic cross that examines the inheritance of two traits simultaneously.

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Test cross

A method used to determine an organism’s genotype by crossing it with a recessive phenotype.

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Linked genes

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

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Recombinants

Offspring that exhibit a combination of traits that differ from those of either parent due to recombination.

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Sex-linked traits

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

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Barr bodies

Inactive X chromosomes in females that are condensed and visible in the nucleus.

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Incomplete dominance

A form of inheritance where neither allele is dominant, resulting in a blended phenotype.

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Codominance

A form of inheritance where both alleles are fully expressed in the phenotype.

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Polygenic inheritance

A form of inheritance where multiple genes interact to determine a single trait.

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Meiosis

A type of cell division that results in four haploid daughter cells, producing gametes.

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Spermatogenesis

The process of producing sperm cells through meiosis.

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Oogenesis

The process of producing egg cells (ova) through meiosis.

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Nondisjunction

The failure of chromosomes to separate correctly during meiosis, resulting in an abnormal number of chromosomes.

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Aneuploidy

A condition involving an abnormal number of chromosomes, such as Down syndrome.