Heredity - Part II

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Last updated 8:58 AM on 3/31/26
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69 Terms

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Nondisjunction

error in meiosis or mitosis in which members of a pair of homologous chromosomes or a pair of sister chromatids fail to separate properly from each other

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n + 1

gametes that form with an extra chromosome; resulting from nondisjunction during meiosis

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n - 1

gametes that form with a missing chromosome; resulting from nondisjunction during meiosis

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Polysomy

type of chromosomal mutation when there is too many copies of a particular chromosome

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Trisomy 21

condition in which an individual has three copies of a chromosome, resulting in Down Syndrome

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Monosomy

condition that occurs when an organism is missing a chromosome

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Karyotype

picture of all the chromosomes in a cell arranged in pairs

<p>picture of all the chromosomes in a cell arranged in pairs</p>
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Polyploidy

condition in which an organism has extra sets of chromosomes

<p>condition in which an organism has extra sets of chromosomes</p>
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Seedless Plants

varieties of plants that develop when an organism is triploid or has an odd number of chromosome sets

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Heredity

passing of traits from parents to offspring, often demonstrating patterns of inheritance

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P generation

first generation of parent organisms in a study

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F generation

subsequent generations in a family of organisms, such as F1 and F2

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Genome

complete genetic information of an organism

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Genotype

combination of alleles an organism has for a specific characteristic within its genome

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Gene

section of the genome that codes for a particular trait

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Allele

version of a gene found at a specific location in the DNA

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Locus

specific place on the chromosome where an allele is located within the DNA

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Law of Dominance

when two different alleles are present in a genotype, only the dominant allele is expressed

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Dominant Allele

trait that is expressed when there is at least one copy

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Recessive Allele

trait that is only expressed when it is the only allele present in the genotype (both alleles must be the same)

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True-Breeding Cross

when purebred organisms that contain genotypes of a single allele type are mated with one another

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Purebred

an organism that only has two of the same allele in its genotype

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Law of Segregation of Alleles

alleles of the same gene do not travel together when chromosomes are placed into gametes

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Monohybrid Cross

occurs when two hybrid parents, each possessing two different alleles for a specific gene, are mated

<p>occurs when two hybrid parents, each possessing two different alleles for a specific gene, are mated</p>
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Punnett Square

tool used to predict offspring genotypes based on parent genotypes

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Homozygous

having two of the same allele

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Heterozygous

having two different alleles

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Phenotype

expression of a genetic trait, such as physical appearance

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Test Cross

used to determine the unknown genotype of an organism displaying a dominant phenotype

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Homozygous Dominant

genotype of the parent in a test cross when all offspring show the dominant phenotype

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Heterozygous

genotype of the parent in a test cross when some of the offspring show the dominant phenotype and some of the offspring show the recessive phenotype

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Dihybrid Cross

occurs when two parents that are both heterozygous for two specific traits are mated

<p>occurs when two parents that are both heterozygous for two specific traits are mated</p>
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2^n, where n is the number of traits that have two options

formula used to determine the number of possible allele combinations in a gamete

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Phenotypic Ratio

relative frequency or amount of each observable phenotype in the offspring

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Non-Mendelian Inheritance

occurs when observed phenotypic ratios deviate from expected ratios

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Simple (Complete) Dominance

one allele is completely dominant and the other is recessive

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3:1

observed ratio of dominant to recessive phenotypes in a monohybrid cross

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9:3:3:1

observed ratio in a dihybrid cross, showing more offspring with both dominant phenotypes and the least offspring with both recessive phenotypes

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1:1:1:1

observed ratio in a dihybrid test cross, showing equal amounts of offspring of both dominant phenotypes as offspring with both recessive phenotypes

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Multiplication Rule of Probability

used to calculate the likelihood of combined events, such as having two different phenotypes

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Epistasis

one gene controls the expression of another gene

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Codominance

both alleles are fully expressed and contribute to the phenotype of a heterozygous organism

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Incomplete Dominance

heterozygous organisms show a blending of two alleles in their phenotype

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1:2:1

phenotypic ratio seen when a monohybrid cross is performed for a trait with incomplete dominance or codominance

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Addition Rule

used when considering the likelihood of getting one phenotype or another

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Mutually Exclusive Traits

characteristics that cannot both occur at that same time, such as dominant and recessive phenotypes for a trait

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Multiple Allele Trait

occurs when there are more than two possible alleles to choose from, such as blood types

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Rh factor

characteristic of blood type that describes the presence of a glycoprotein found on red blood cells

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Gene Linkage

occurs when two different genes are located on the same chromosome and are inherited together

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Crossing Over

meiotic process that can break the linkage between two genes

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Independent Assortment

random distribution of alleles among gametes that is unable to occur when genes are linked

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Autosomal Trait

found on chromosomes that are common to males and females; characteristic that appears equally in males and females

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Sex-Linked Trait

found on the last pair of chromosomes; most commonly X-linked (not

found on the Y chromosome)

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X-Linked Trait

shows different inheritance patterns

for males and females

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Pedigree

diagram that shows inheritance of a particular trait through a family; allows us to determine whether a trait is dominant/recessive and autosomal/sex-linked

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Recessive Inheritance Pattern

often shows that a trait can be hidden

<p>often shows that a trait can be hidden</p>
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Dominant Inheritance Pattern

often appears in each generation of a family and cannot be hidden

<p>often appears in each generation of a family and cannot be hidden</p>
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Sex-Linked Dominant Pattern

affected fathers have affected daughters; unaffected mothers have unaffected sons

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Sex-Linked Recessive Pattern

unaffected fathers have unaffected daughters; affected mothers have affected sons

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Chromosome Map

shows the amount of distance between

two genes that are located on the same chromosome

<p>shows the amount of distance between</p><p>two genes that are located on the same chromosome</p>
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Closely Linked Genes

recombination and crossing over will occur less often

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Distantly Linked Genes

recombination and crossing over will occur more often

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Recombination Frequency

number of times crossing over occurred compared to the total number of offspring

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Chi-Square Test

determines "goodness of fit" of experimental data; if data "fits the expectation," the number calculated will be low

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Critical Value

highest number calculated by Chi-Square that is permitted to support a hypothesis

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Degrees of Freedom

(number of groups tested in an experiment) - 1

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Epigenetics

occurs when the environment influences the activity and expression of genes

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DNA Methylation

decreases the expression of genes in the affected DNA region

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Histone Modification

causes condensation or compacting of the DNA to prevent gene expression

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