Unit 5 AP Biology vocab terms

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29 Terms

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Allele

A variant form of a gene that is located at a specific position on a specific chromosome.

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Aneuploid

An organism with an abnormal number of chromosomes, not an exact multiple of the haploid number.

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Autosome

Any chromosome that is not a sex chromosome, typically found in pairs in diploid organisms.

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Chromosome map

A diagram that shows the relative positions of genes on a chromosome.

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Crossing over

The exchange of genetic material between homologous chromosomes during meiosis.

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Diploid

A cell or organism that has two sets of chromosomes, one from each parent.

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Dominant

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

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Euploid

An organism or cell with a complete set of chromosomes, typically a multiple of the haploid number.

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Gamete

A reproductive cell (sperm or egg) that contains half the genetic material of an organism.

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Genotype

The genetic constitution of an organism, represented by its alleles.

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Haploid

A cell or organism that has a single set of chromosomes.

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Heterozygous

An individual with two different alleles for a particular gene.

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Homologous chromosomes

Pairs of chromosomes that are similar in shape, size, and genetic content.

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Homozygous

An individual with two identical alleles for a particular gene.

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Independent assortment

The random distribution of alleles during gamete formation.

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Linked genes

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

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Monosomy

The condition of having one less than the diploid number of chromosomes.

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Nondisjunction

The failure of homologous chromosomes or sister chromatids to separate properly during meiosis.

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Phenotype

The physical expression or characteristics of an organism's genotype.

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Recessive

An allele that is masked by the presence of a dominant allele in the phenotype.

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Recombinant chromosome

A chromosome created by the combination of genetic material through crossing over.

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Recombination frequency

The frequency of recombination between two genes, used to determine their distance apart on a chromosome.

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Sex chromosome

A chromosome that determines the sex of an individual, typically X or Y in humans.

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Sex-linked trait

A trait associated with a gene located on a sex chromosome.

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Somatic cell

Any cell of the body except for germ cells (sperm and egg).

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Tetrad

A structure that forms during meiosis consisting of four chromatids, or two homologous chromosomes.

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Trisomy

The condition of having an extra chromosome, resulting in three copies of a particular chromosome.

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Zygote

The fertilized ovum, the result of the union of a sperm and egg.

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Phenotypic plasticity

The ability of an organism to change its phenotype in response to environmental conditions.