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Heredity II 2
Heredity II 2
INCOMPLETE DOMINANCE occurs when the combination of two alleles produce a new
intermediate phenotype that is not manifested in either parent.
An interesting case of codominance and multiple allelism is the blood type AB0:
GENOTYPE AA A0 BB B0 AB 00
PHENOTYPE AB 0
A B
Antigen A and B No antigens
A B
Antibodies Anti-B Anti-A No antibodies Anti-A and Anti-B
The information about antigens and antibodies is not necessary to do the exercises, but it
explain why the 0 group is the universal donor, and why we can receive blood from one person
or not.
The X chromosome is bigger than the Y chromosome and it includes more genes.
Some traits are determined by genes that are located in X chromosome but not in the Y
chromosome . These are the cases of haemophilia and colour blindness.
Both disorders are produced by recessive alleles, in front of the normal ones.
In Haemophilia:
XA XA : healthy woman
XA Xa : carrier woman (she is a healthy woman, but she can transmit the disease to her
descendants)
Xa Xa : haemophiliac woman
XA Y : healthy man
Xa Y: haemophiliac man
Example:
A healthy woman whose father is a haemophiliac, has a son with a healthy man. Describe the
possible descendants.
Descendants:
25% healthy women XA XA
25% healthy men XA Y
25% healthy women (carrier) XA Xa
25% haemophilic men Xa Y