Respuesta :
X-linked genes are inherited. The affected girl's father is hemophilic (X-Y), and the mother might be either hemophilic (X-X-) or carrier normal (X+X-).
What are the X-linked genes?
These are the genes located in the X séx chromosome and not in the somatic ones.
Traits coded by these genes are inherited. This is, X-linked genes are transmitted from parents to children through generations.
According to this, X-linked genetic disorder will be inherited as well.
- Men have a high probability of being affected since they only have one copy of the X chromosome.
- In women, the effect of the mutation might be musk in heter0zyg0us state.
Hemophilia is a X-linked recessive genetic disorder.
Let us represent the recessive allele with the symbol -, and the dominant allele with the symbol +.
- X- is the chromosome carrying the recessive allele
- X+ is the chromosome carrying the dominant allele
For the affection to be expressed, the person must be either,
- X-X- ⇒ woman/girl
- X-Y ⇒ man/boy
If the baby girl is found to have inherited the trait from her parents, then her genotype is X-X-. She must have received one X- chromosomes from each parent.
- Her father provided the X chromosome, so he must be hemophilic (X-Y)
- Her mother provided the other X chromosome, but she can be either a carrier (heter0zyg0us, X+X-) or hemophilic (h0m0zyg0us recessive, X-X-).
Options,
Cross 1) affected father x carrier mother
Parentals) X-Y x X+X-
Gametes) X- Y X+ X-
Punnett square) X- Y
X+ X+X- X+Y
X- X-X- X-Y
F1) 1/2 = 50% of the progeny is expected to be healthy (25% X+X- girls + 25% X+Y boys)
1/2 = 50% of the progeny is expected to be hemophilic (25% X-X- girls + 25% X-Y boys)
Cross 2) affected father x affected mother
Parentals) X-Y x X-X-
Gametes) X- Y X- X-
Punnett square) X- Y
X- X-X- X-Y
X- X-X- X-Y
F1) 100% of the progeny is expected to be hemophilic (50% X-X- girls + 50% X-Y boys)
- the phenotype of the father ⇒ hemophilic (X-Y)
- the phenotype of the mother ⇒ normal carrier (X+X-) or hemophilic (X-X-)
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