HUMAN GENETICS

profileJRAE79
lab_report_-_wk_15_humangenetics2.docx

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