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Alleles
different variations of the same gene
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)
Autosomal Recessive
most common inheritance pattern, rare in family, males and females are equally likely to inherit the disease, often skips generation
Autosomes
chromosomes 1-44 in a human
Blood Type
codominance (type AB is fully A and fully B) and multiple alleles (A, B, and i)
Carrier
someone who carries the recessive trait, but doesn't show it due to having a dominant X to mask it
Chromosome Mutation
often happen during meiosis, changing the number or location of genes
Chromosome Theory of Inheritance
genes are located on chromosomes and the behavior of chromosomes during meiosis accounts for inheritance patterns
Codominance
both traits are fully and seperately expressed
Cross
matching of two organisms
crossing a brown horse and a white horse create an appaloosa horese (white horse with brown spots)
What is an example of Codominance?
crossing red and white flowers make pink flowers
What is an example of incomplete dominance?
Dihybrid Cross
used when finding the possible genotypes for offspring when considering two traits at the same time
DNA
the macromolecule that has the instructions for making you who you are
Dominant
if present, allele will always have that trait expressed
Down Syndrome, Klinefelter's Syndrome, turner's sybdrome
What are examples of chromosome mutations?
Duplication
changes the size of chromosomes and results in multiple copies of a single gene
few genes
What does the Y chromosome contain?
Frameshift Mutations
the insertion or deletion of a nucleotide
Gene
section of DNA that provides the instructions for making a protein
Gene Mutation
happen during DNA replication and cause a change to the original DNA sequence
Genotype
the actual alleles inherited (FF, Ff, or ff)
Germ line mutation
occur in germ line cells that give rise to gametes and are passed on by meiosis creating a mutated offspring
Gregor Mendel
Austrian monk who used pea plants to learn about genetics, "father of genetics"
Heterozygous
two different alleles (Aa)
Homologous Chromosomes
the matching chromosomes from our mom and dad
Homozygous
two of the same alleles (AA or aa)
Incomplete Dominance
the heterozygous phenotype is somehwhere between the two homozygous phenotypes, neither allele is completely dominant or recessive
Law of Dominance
a dominant allele will express itself over a recessive allele
Law of Independent Assortment
the assortment of chromosomes for one trait doesn't affect the assortment of chromosomes for another trait
Law of Segrgation
when chromosomes seperate in meiosis, each gamete will receive only one chromosome from each pair
Linked Genes
genes that are physically located on the same chromosome will be inherited together
many genes that affect many traits
What does the X chromosome contain?
mistakes made during DNA replication, mitosis, meiosis, or ptotein synthesis
What causes mutations?
Monohybrid cross
a cross between two organisms looking at one trait
Multiple Alleles
having more than two alleles for one gene
Mutagens
chemical that can cause DNA mutations
Mutation
any change in DNA
Nondisjunction
chromosomes do not seperate correctly during anaphase, resulting in 1 or 3 chromosomes instead of two per cell
Pedigree
chart used to trace the phenotypes and genotypes in a family to determine whether people carry diseases or traits
Phenotype
the physical traits/characteristics seen in an organism (purple flowers)
Point Mutations
substitute one nucleotide for another
Polygenic Inheritance
A trait produced by two or more genes
protein
macromolecule that runs your body and expresses your traits
Punnett Square
a diagram that shows the probability of inheriting traits from parents with certain genes
Purebred
type of organism whose ancestors are genetically uniform
Recessive
allele will only have that trait expressed when the dominant allele is not present
Sex Linked Gene
gene located on a sex chromosome
Sex-Linked Recessive
rare in the family, males more often affected, often skips generations
Sex-Linked Traits
traits that are inherited with sex chromosomes, males have XY and females have XX, determine the biological sex of an individual
Somatic Mutations
occur in somatic cells and are passed on by mitosis and form cancer
Translocation
nonhomologous chromosomes exchange segments
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