Unit 6 Genetics and Herdity

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53 Terms

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Alleles

different variations of the same gene

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Autosomal Dominant

common in the family, males and females are equally likely to inherit the disease, never skips a generation (a child can't inherit the disease if both parents are healthy)

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Autosomal Recessive

most common inheritance pattern, rare in family, males and females are equally likely to inherit the disease, often skips generation

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Autosomes

chromosomes 1-44 in a human

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Blood Type

codominance (type AB is fully A and fully B) and multiple alleles (A, B, and i)

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Carrier

someone who carries the recessive trait, but doesn't show it due to having a dominant X to mask it

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Chromosome Mutation

often happen during meiosis, changing the number or location of genes

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Chromosome Theory of Inheritance

genes are located on chromosomes and the behavior of chromosomes during meiosis accounts for inheritance patterns

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Codominance

both traits are fully and seperately expressed

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Cross

matching of two organisms

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crossing a brown horse and a white horse create an appaloosa horese (white horse with brown spots)

What is an example of Codominance?

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crossing red and white flowers make pink flowers

What is an example of incomplete dominance?

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Dihybrid Cross

used when finding the possible genotypes for offspring when considering two traits at the same time

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DNA

the macromolecule that has the instructions for making you who you are

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Dominant

if present, allele will always have that trait expressed

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Down Syndrome, Klinefelter's Syndrome, turner's sybdrome

What are examples of chromosome mutations?

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Duplication

changes the size of chromosomes and results in multiple copies of a single gene

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few genes

What does the Y chromosome contain?

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Frameshift Mutations

the insertion or deletion of a nucleotide

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Gene

section of DNA that provides the instructions for making a protein

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Gene Mutation

happen during DNA replication and cause a change to the original DNA sequence

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Genotype

the actual alleles inherited (FF, Ff, or ff)

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Germ line mutation

occur in germ line cells that give rise to gametes and are passed on by meiosis creating a mutated offspring

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Gregor Mendel

Austrian monk who used pea plants to learn about genetics, "father of genetics"

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Heterozygous

two different alleles (Aa)

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Homologous Chromosomes

the matching chromosomes from our mom and dad

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Homozygous

two of the same alleles (AA or aa)

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Incomplete Dominance

the heterozygous phenotype is somehwhere between the two homozygous phenotypes, neither allele is completely dominant or recessive

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Law of Dominance

a dominant allele will express itself over a recessive allele

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Law of Independent Assortment

the assortment of chromosomes for one trait doesn't affect the assortment of chromosomes for another trait

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Law of Segrgation

when chromosomes seperate in meiosis, each gamete will receive only one chromosome from each pair

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Linked Genes

genes that are physically located on the same chromosome will be inherited together

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many genes that affect many traits

What does the X chromosome contain?

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mistakes made during DNA replication, mitosis, meiosis, or ptotein synthesis

What causes mutations?

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Monohybrid cross

a cross between two organisms looking at one trait

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Multiple Alleles

having more than two alleles for one gene

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Mutagens

chemical that can cause DNA mutations

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Mutation

any change in DNA

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Nondisjunction

chromosomes do not seperate correctly during anaphase, resulting in 1 or 3 chromosomes instead of two per cell

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Pedigree

chart used to trace the phenotypes and genotypes in a family to determine whether people carry diseases or traits

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Phenotype

the physical traits/characteristics seen in an organism (purple flowers)

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Point Mutations

substitute one nucleotide for another

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Polygenic Inheritance

A trait produced by two or more genes

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protein

macromolecule that runs your body and expresses your traits

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Punnett Square

a diagram that shows the probability of inheriting traits from parents with certain genes

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Purebred

type of organism whose ancestors are genetically uniform

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Recessive

allele will only have that trait expressed when the dominant allele is not present

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Sex Linked Gene

gene located on a sex chromosome

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Sex-Linked Recessive

rare in the family, males more often affected, often skips generations

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Sex-Linked Traits

traits that are inherited with sex chromosomes, males have XY and females have XX, determine the biological sex of an individual

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Somatic Mutations

occur in somatic cells and are passed on by mitosis and form cancer

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Translocation

nonhomologous chromosomes exchange segments

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X-Lined Genes

females inherit X-linked genes as normal and the principle of dominance applies since they have 2 X's so they inherit two copies of the gene