Scribd
Upload
197 views4 pages

MIT7 01SCF11 3.3prob1

This document contains practice problems about interpreting pedigrees and determining modes of inheritance for genetic diseases. It includes questions about identifying the most likely mode of inheritance from pedigrees, determining genotypes of individuals, and calculating probabilities of offspring being affected or carriers. The questions cover autosomal dominant, autosomal recessive, and X-linked inheritance patterns.

Uploaded by

Maureen Gutierrez
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
197 views4 pages

MIT7 01SCF11 3.3prob1

This document contains practice problems about interpreting pedigrees and determining modes of inheritance for genetic diseases. It includes questions about identifying the most likely mode of inheritance from pedigrees, determining genotypes of individuals, and calculating probabilities of offspring being affected or carriers. The questions cover autosomal dominant, autosomal recessive, and X-linked inheritance patterns.

Uploaded by

Maureen Gutierrez
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
You are on page 1/ 4

Practice Problems for Genetics, Session 3: Pedigrees

Question 1
In the following human pedigrees, the filled symbols represent the affected individuals. You may assume that the
disease allele is rare and therefore individuals marrying into the family are unlikely to have defective allele.
a)
1
2
4 5
3
i) What is the most likely mode of inheritance for this pedigree?
ii) State the genotypes of individuals # 1-5 in the following table using the letter A. Use the uppercase
letter to represent the dominant allele and lowercase letter to represent the recessive allele.
Individual Genotype
#1
#3
#4
#5
iii) If individuals # 2 and 3 have another son what are the chances that this son will be affected?
b)
7
8
6
i) What is the most likely mode of inheritance for this pedigree?
ii) State the genotypes of individuals # 6-8 in the following table using the letter B. Use the uppercase
letter to represent the dominant allele and lowercase letter to represent the recessive allele.
Individual Genotype
#6
#7
#8
iii) If Individuals #6 and #7 have another daughter what are the chances that she will be affected.

Question 2
You are analyzing the following human pedigree.
Assume that the individual marked with an asterisk (*) does not carry any allele associated with the affected
phenotype and that no other mutation spontaneously occurs. Also assume complete penetrance. Use R or X
R

for the allele associated with the dominant phenotype, r or X
r
for the allele associated with the recessive
phenotype.
1 2
3
? ?
*
affected female
affected male
Unaffected female
Unaffected male
A
B
a) What is the most likely mode of inheritance of this disease? Choose from: autosomal dominant, autosomal
recessive, X-linked dominant, X-linked recessive.
b) List all possible genotypes of the following individuals in the pedigree.
Individuals Genotypes
#1
#3
c) What is the probability of Individual A being affected?
d) What is the probability of Individual B being affected?
Question 3
The following human pedigree shows a family affected by a specific disease.
Assume that the individuals marked with an asterisk (*) do not carry any allele associated with the affected
phenotype and that no other mutation spontaneously occurs. Also assume complete penetrance
affected female
affected male
Unaffected female
Unaffected male
2
1
4
5
3
1
st
Pedigree
a) State the most likely mode of inheritance for this disease. Choose from: autosomal dominant, autosomal
recessive, X-linked dominant, X-linked recessive.
Question 3, continued
b) Write all possible genotypes of the following individuals in the pedigree. Use the uppercase A for the allele
associated with the dominant phenotype and lowercase a for the allele associated with the recessive phenotype.
Individuals All possible Genotypes
#1
#2
#4
c) What is the probability that Individual 5 will be a carrier?
d) The following human pedigree shows a family affected by a different disease. Assume that the individuals
marked with an asterisk (*) do not carry any allele associated with the affected phenotype and that no other
mutation spontaneously occurs. Also assume complete penetrance. State the most likely mode of inheritance for
this disease.
6
2
nd
Pedigree
Note: Use the notation such as R or X
R
for the
*
allele associated with the dominant phenotype and
r or X
R
for the allele associated with the recessive
phenotype.
*
e) Individual 3 from the 1st pedigree has a second marriage with Individual 6 from the 2nd pedigree. They have a
son and a daughter as shown below.
Individual 3 Individual 6 from
from 1
st
Pedigree
? ?
2
nd
Pedigree
i) What would be the genotype of their son for the two disease genes?
i) What would be the genotype of their daughter for the two disease genes?
MIT OpenCourseWare
http://ocw.mit.edu
7.01SC Fundamentals of Biology
Fall 2011
For information about citing these materials or our Terms of Use, visit: http://ocw.mit.edu/terms.

You might also like