exam 3 Flashcards
how many pairs of chromosomes are there
23 pairs
what is a genotype
our DNA
what is the difference between a heterozygous genotype and a homozygous genotype
heterozygous genotype: copies are different alleles
homozygous genotype: both copies are the same allele
what is a phenotype
our observable characteristics or traits
what affects your phenotype
our genes, environment, and chance define your phenotype
what does it mean to say a trait is dominant or recessive
dominant- shown when a person only has one copy of that gene
recessive- when two copies of that gene is present
what are the genotype and phenotype of someone who is a carrier
the trait is only shown on the recessive gene
ex: Aa
what is incomplete dominance
phenotype of the heterozygote is intermediate between the two homozygotes Cs = wavy hair (CC =curly and ss = straight)
how does meiosis halve the number of chromosomes per cell
lines them up along the midline and then pulls them apart into two separate cells
what is the difference between autosomes and sex chromosomes
22 pairs of autosomes and 1 pair of sex chromosomes
male genotype
X Y
what is the location and function of the SRY gene
located on the Y chromosome, has instructions for making,ing a regular protein, signals for gonads to develop into testes
what is a sex-linked trait
located on either the X or Y chromosome
how can you use a Punnet square to predict the probabilities of X-linked phenotypes for children given the genotypes of the parents
you can match the two genotypes of each parent to make a percentage of their chances to get certain traits
what are the symbols used in pedigrees
X Y