The basic building block of all life.
What is DNA?
The base that appears only in RNA.
What is uracil?
A change to a DNA sequence.
What is a mutation?
The physical characteristics expressed by an organism.
What is a phenotype?
An open square represents this kind of individual.
What is an unaffected male?
The monomer of DNA.
What is a nucleotide?
To match or fit in correctly, like a puzzle piece.
What is complementary?
This mutation is found in a single DNA base pair.
What is a point mutation?
This inheritance pattern involves dominant alleles being expressed over their recessive counterparts.
What is autosomal?
Pedigrees are numbered using this style of numerals.
What are Roman numerals?
The shape of DNA.
What is a double helix?
A series of three base pairs.
What is a codon?
This special genetic test is how scientists can view possible chromosomal mutations.
What is a karyotype?
This inheritance pattern involves the blending of two dominant phenotypes into a third.
What is incomplete dominance?
An individual that possesses a recessive trait but does not express that trait is called this.
What is a carrier?
These are the four nitrogen bases to DNA.
What are adenine, guanine, cytosine and thymine?
This codon signals for the process of translation to begin.
What is methionine (start codon)?
This chromosomal mutation involves changing the placement of genes within the same chromosome.
What is inversion?
Perform the following cross:
A homozygous recessive individual is crossed with a heterozygous individual. What is the possibility to have recessive offspring?
What is 50%?
The expressed trait is inherited in what manner?
What is dominant?
Nitrogen bases are held together by this style of bond.
What is a hydrogen bond?
Translate the following sequence:
AUG-GCA-UAU-CAG-UGA
What is methionine-alanine-tyrosine-glutamine-stop?
This mutation causes the entire codon "sentence" to be read differently than how it should.
What is a frameshift mutation?
Perform the following cross:
Color blindness is an X-linked recessive allele.
A man affected by color blindness marries a woman who is a carrier for colorblindness. What is the chance of their daughters being colorblind?
What is 25%?
What is the likely genotype of individual III-3?
What is heterozygous dominant? (carrier)