Genetics of Colorblindness

Genetics of Colorblindness

Assessment

Interactive Video

Biology, Science, Other

9th - 12th Grade

Hard

Created by

Patricia Brown

FREE Resource

The video discusses the genetics of colorblindness, focusing on its X-linked inheritance pattern. It explains how cone cells and opsins are involved in color perception, with specific genes located on the X chromosome. The video details the conditions under which colorblindness occurs in males and females, emphasizing the recessive nature of the trait. It also explores genetic crosses and the resulting F1 generation, highlighting how colorblindness can manifest in offspring. The video concludes with a summary of the key points discussed.

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10 questions

Show all answers

1.

MULTIPLE CHOICE QUESTION

30 sec • 1 pt

What is the genetic basis of colorblindness?

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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