HUMAN GENETICS
Human Genetics
Hands-on labs, inc. Version 42-0059-00-01
PHOTOS: There are no photos to be included with this lab report.
Exercise 1: genotype to Phenotype
Observations
Experiment
Human Genetics
281
©Hands-On Labs, Inc.
www.LabPaq.com
|
Data Table 1: Trait Characteristics for Exercise 1 |
|||||
|
# |
Trait |
Allele from Mother |
Allele from Father |
Child’s genotype |
Child’s Phenotype (written) |
|
1 |
Face shape
● AA, Aa aa
● Round Square |
A or a |
A or a |
|
|
|
2 |
Chin size
● BB, Bb bb
● Prominent Average |
B or b |
B or b |
|
|
|
3 |
Cleft chin
● CC, Cc cc
● Cleft chin No cleft |
C or c |
C or c |
|
|
|
4 |
Hair type
● DD Dd dd
● Straight Wavy Curly |
D or d |
D or d |
|
|
|
5 |
Widow’s peak
● EE, Ee ee
● Widows peak Absent |
E or e |
E or e |
|
|
|
6 |
White forelock
● FF, Ff ff
● White forelock Absent |
F or f |
F or f |
|
|
|
7 |
Eye shape
● GG, Gg gg
● Almond shape Round shape |
G or g |
G or g |
|
|
|
8 |
Eye slantedness
● HH, Hh hh
● Horizontal Upward slant |
H or h |
H or h |
|
|
|
9 |
Eyelashes
● II, Ii ii
● Long lashes Short lashes |
I or i |
I or i |
|
|
|
10 |
Eyebrow thickness
● JJ, Jj jj
● Thick Thin |
J or j |
J or j |
|
|
|
11 |
Eyebrow length
● KK, Kk kk
● Separated brows Brows joined |
K or k |
K or k |
|
|
|
12 |
Lip thickness
● LL, Ll ll
● Thick lips Thin lips |
L or l |
L or l |
|
|
|
13 |
Dimples
● MM, Mm mm
● Dimples No dimples |
M or m |
M or m |
|
|
|
14 |
Nose shape
● NN, Nn nn
● Round Pointed |
N or n |
N or n |
|
|
|
15 |
Nostril shape
● OO, Oo oo
● Round Pointed |
O or o |
O or o |
|
|
|
16 |
Earlobe attachment
● PP, Pp pp
● Free Attached |
P or p |
P or p |
|
|
|
17 |
Darwin’s earpoint
● QQ, Qq qq
● Pointed Point absent |
Q or q |
Q or q |
|
|
|
18 |
Cheek freckles
● SS, Ss ss
● Present Absent |
S or s |
S or s |
|
|
|
19 |
Forehead freckles
● TT, Tt tt
● Forehead freckles Absent |
T or t |
T or t |
|
|
Exercise 1: genotype to Phenotype
Observations
A. Why was the male chosen to determine the sex of the child?
B. Draw a picture of the compiled traits.
C. If this activity was repeated two or three times would the offspring images change? Explain
your answer.
Exercise 2: Punnett Squares
Questions
Use a Punnett square to solve the following scenarios. You MUST INCLUDE THE PUNNET SQUARE AS PART OF YOUR ANSWER FOR EACH OF THESE PROBLEMS.
A. Dominant: cheek freckles
Recessive: no cheek freckles
(Please note that this trait is more complicated than described in this lab exercise, but for learning purposes, assume that this is correct.)
A man with a heterozygous gene for freckles on his cheeks has a child with a woman who does not have freckles on her cheeks. What is the likelihood that their son will have freckles on his cheeks?
B. Dominant: normal; no cystic fibrosis
Recessive: cystic fibrosis
A woman has a history of cystic fibrosis in her family, and found out that she has the gene for cystic fibrosis, but is not affected by the gene. Her husband also has a history of cystic fibrosis in his family. He got tested yesterday and found that he is also a carrier for the disease, but is not affected by it. They are going to have a baby in two months. What is the likelihood that their baby will have cystic fibrosis?
C. Dominant: normal; no Tay-Sachs
Recessive: Tay-Sachs
A man is a carrier for Tay-Sachs. He is going to have a child with a woman who has homozygous normal genes. What are the chances that they will have a child who has Tay-Sachs disease?
D. Dominant: Round face Dominant: Prominent chin
Recessive: Square face Recessive: Non-prominent chin
(Please note that this trait is more complicated than described in this lab exercise, but for learning purposes, assume that this is correct.)
A woman with heterozygous genes for a round face shape and a chin that is not prominent has a child with a man who has a square face and homozygous genes for a prominent chin. What are the chances that the child has a square face with a prominent chin?
E. Dominant: Huntington’s disease Dominant: normal; no cystic fibrosis
Recessive: normal; no Huntington’s Recessive: cystic fibrosis
A man with Huntington’s disease is also a carrier for cystic fibrosis. His wife has cystic fibrosis but does not have Huntington’s disease. If they have a baby, what is the likelihood that the baby will have both Huntington’s disease and cystic fibrosis?
F. X-linked dominant trait: no color blindness
X-linked recessive trait: color blindness
A color-blind man marries a non-color-blind woman who is not a carrier for color blindness. What are the chances that they will have a son who is also color-blind?
What are the chances that they will have a daughter who is a carrier for color blindness?
Omit pedigrees.
Ex
p
e
ri
m
e
n
t
Hu
ma
n
G
e
n
e
t
i
c
s
28
1
©
H
a
nds
-
On
L
a
bs,
I
n
c
.
ww
w
.
L
a
b
P
a
q
.
c
o
m
Human Gen
e
tics
Hands
-
on
l
a
b
s,
i
nc.
V
e
r
sion
42
-
0059
-
00
-
01
PHOTOS: There are no photos to be included with this lab report.
E
x
e
r
cise 1:
g
enotype
t
o
Phenotype
Observations
Experiment
Human Genetics
28
1
©Hands-On Labs, Inc.
www.LabPaq.com
Human Genetics
Hands-on labs, inc. Version 42-
0059-00-01
PHOTOS: There are no photos to be included with this lab report.
Exercise 1: genotype to Phenotype
Observations