What is the genetic basis of colorblindness?

Genetics of Colorblindness

Interactive Video
•
Biology, Science, Other
•
9th - 12th Grade
•
Hard

Patricia Brown
FREE Resource
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10 questions
Show all answers
1.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Mitochondrial inheritance
Autosomal dominant inheritance
X-linked inheritance
Y-linked inheritance
2.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Why is colorblindness often referred to as red and green colorblindness?
Because the genes for red and green opsins are on the X chromosome
Because it is linked to the Y chromosome
Because it affects the perception of all primary colors
Because it affects only the perception of blue
3.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What type of cone cells are responsible for detecting blue light?
L-type cone cells
M-type cone cells
S-type cone cells
All cone cells
4.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
Where are the genes for S-type opsins located?
Chromosome 21
Y chromosome
X chromosome
Chromosome 7
5.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What does X-linked recessive inheritance mean?
The trait is passed from mother to daughter
The trait is passed from father to son
Only one allele needs to be mutated for the trait to be expressed
Both alleles must be mutated for the trait to be expressed
6.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
In males, what condition leads to colorblindness?
Having no X chromosome
Having a defective Y chromosome
Having one defective X chromosome
Having two X chromosomes
7.
MULTIPLE CHOICE QUESTION
30 sec • 1 pt
What is the genotype of a carrier female for colorblindness?
XcXc
XcY
XnXn
XnXc
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