The major phenotype of deficiency of protolithic enzyme alpha-antitrypsin is the destruction of pulmonary alveoli resulting in chronic obstructive pulmonary disease or emphysema. The gene for this enzyme is highly polymorphic, with more than 70 different alleles described. 90% of white Europeans have MM genotype (normal). Two mutant alleles, S and Z, account for most of the disease associated with alpha-antitrypsin deficiency. The flowing table tabulates frequencies of different clinically important genotypes in the French population. Genotype Frequency MM 0.90 MZ 0.04 SS 0.001 SZ 0.0012 ZZ 0.0004 Using the data presented, calculate the allele frequencies for Z and S.
The major phenotype of deficiency of protolithic enzyme alpha-antitrypsin is the destruction of pulmonary alveoli resulting in chronic obstructive pulmonary disease or emphysema. The gene for this enzyme is highly polymorphic, with more than 70 different alleles described. 90% of white Europeans have MM genotype (normal). Two mutant alleles, S and Z, account for most of the disease associated with alpha-antitrypsin deficiency. The flowing table tabulates frequencies of different clinically important genotypes in the French population. Genotype Frequency MM 0.90 MZ 0.04 SS 0.001 SZ 0.0012 ZZ 0.0004 Using the data presented, calculate the allele frequencies for Z and S.
Human Anatomy & Physiology (11th Edition)
11th Edition
ISBN:9780134580999
Author:Elaine N. Marieb, Katja N. Hoehn
Publisher:Elaine N. Marieb, Katja N. Hoehn
Chapter1: The Human Body: An Orientation
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
Transcribed Image Text:The major phenotype of deficiency of protolithic enzyme alpha-antitrypsin is the
destruction of pulmonary alveoli resulting in chronic obstructive pulmonary
disease or emphysema. The gene for this enzyme is highly polymorphic, with
more than 70 different alleles described. 90% of white Europeans have MM
genotype (normal). Two mutant alleles, S and Z, account for most of the disease
associated with alpha-antitrypsin deficiency. The flowing table tabulates
frequencies of different clinically important genotypes in the French population.
Genotype
Frequency
MM
0.90
MZ
0.04
SS
0.001
SZ
0.0012
ZZ
0.0004
Using the data presented, calculate the allele frequencies for Z and S.
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