Apologia Biology 2nd edition Module 8

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24 Terms

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true breeding

if an organism has a certain characteristic that is always passed on to its offspring, we say that this organism bred true with respect to that characteristic

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allele

one of a pair of genes that occupies the same position on homologous chromosomes

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genotype

a two-letter set that represents the alleles an organism possesses for a certain trait

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phenotype

the observable expression of an organism's genes

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homozygous genotype

a genotype in which both alleles are identical

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heterozygous genotype

a genotype with two different alleles

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dominant allele

an allele that will determine the phenotype if just one is present in the genotype

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recessive allele

an allele that will not determine the phenotype unless the genotype is homozygous

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Mendel's principal #1 of genetics

The traits of an organism are determined by its genes.

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Mendel's principal #2 of genetics

each organism has two alleles that make up the genotype for a given trait

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Mendel's principal #3 of genetics

in sexual reproduction, each parent contributes ONLY ONE of its alleles to the offspring

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Mendel's principal #4 of genetics

In each genotype, there is a dominant allele. If it exists in an organism, the phenotype is determined by that allele.

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Pedigree

a diagram that follows a particular phenotype through several generations

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monohybrid cross

a cross between two individuals, concentrating on only one definable trait

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Dihybrid cross

a cross between two individuals, concentrating on two definable traits

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autosomes

chromosomes that do not determine the sex of an individual

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sex chromosomes

chromosomes that determine the sex of an individual

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antigen

a protein that, when introduced in the blood, triggers the production of an antibody

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autosomal inheritance

inheritance of a genetic trait not on a sex chromosome

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genetic disease carrier

a person who is heterozygous in a recessive genetic disorder

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sex-linked inheritance

inheritance of a genetic trait located on a sex chromosome

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mutation

a radical chemical change in one or more alleles

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change in chromosome structure

a situation in which a chromosome loses or gains genes during meiosis

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change in chromosome number

a situation in which abnormal cellular events in meiosis lead to either none of a particular chromosome in the gamete or more than one chromosome in the gamete