Genetic Inheritance

Quiz
•
Science
•
7th Grade
•
Hard
Standards-aligned
Lisa Thompson
FREE Resource
15 questions
Show all answers
1.
MULTIPLE CHOICE QUESTION
1 min • 1 pt
In the case of mitochondrial inheritance, if a woman with a mitochondrial disorder has children, what percentage of her children are expected to inherit the disorder?
0%
25%
50%
100%
Answer explanation
Mitochondrial disorders are passed down from the mother to all her children, resulting in 100% of her children inheriting the disorder.
2.
DROPDOWN QUESTION
1 min • 1 pt
What is the expected phenotype ratio in the offspring when two individuals heterozygous for a codominant trait mate?
1:2:1
3:1
9:3:3:1
1:1
Answer explanation
When two individuals heterozygous for a codominant trait mate, the expected phenotype ratio in the offspring is 1:2:1, representing the genotypes of homozygous dominant, heterozygous, and homozygous recessive, respectively.
3.
DROPDOWN QUESTION
1 min • 1 pt
An individual with two different alleles for a specific trait is said to be: (a)
homozygous
heterozygous
homogeneous
heterogeneous
Answer explanation
An individual with two different alleles for a specific trait is said to be heterozygous.
4.
DRAG AND DROP QUESTION
1 min • 1 pt
How many males are shown in this pedigree? (a)
8
5
2
16
Answer explanation
There are 8 males shown in the pedigree. This is determined by counting the number of male symbols in the pedigree diagram.
5.
DROPDOWN QUESTION
1 min • 1 pt
In this pedigree, (a) can be carriers of colorblindness and not have it.
Just males
Just females
Both genders
Answer explanation
Only females can be carriers of colorblindness and not have it, as they inherit the trait on the X chromosome and can have one normal X chromosome to compensate.
6.
DROPDOWN QUESTION
1 min • 1 pt
Cystic Fibrosis is a recessive trait. A heterozygous genotype (Cc) will show the phenotype (a) .
CC
Cc
cc
Normal (unaffected or carrier)
Cystic Fibrosis (affected)
Answer explanation
A heterozygous genotype (Cc) for Cystic Fibrosis will show the Normal (unaffected or carrier) phenotype as it is a recessive trait.
Tags
NGSS.HS-LS3-1
NGSS.HS-LS3-2
7.
DROPDOWN QUESTION
1 min • 1 pt
A woman with an X-linked dominant disorder has children with a man who does not have the disorder. The probability that their son will inherit the disorder is (a) .
0%
25%
50%
100%
Answer explanation
The son has a 50% chance of inheriting the X-linked dominant disorder from the mother, as he will receive either her affected X chromosome or the father's Y chromosome.
Tags
NGSS.HS-LS3-1
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