The scenario will be Son: 25% colorblind daughter: 25% colorblind son: 25% of carrier daughters with normal vision: 25% normal son
<h3>What is color blindness?</h3>
The condition is frequently inherited. Certain eye diseases and medications are also possible causes. Men are more affected than women.
Color blindness is characterized by the inability to distinguish between red and green shades.
A colorblind man's genotype is XcY, and a heterozygous carrier female's genotype is XcX. A cross between XcY and XcX would result in progeny with the following ratio=
Son: 25% colorblind daughter: 25% colorblind son: 25% of carrier daughters with normal vision: 25% normal son.
Thus, the couple is likely to have a son who is half normal and half affected. Similarly, the couple is likely to have 50% normal daughters and 50% colorblind daughters.
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Answer:
The mutation is on chromosome/karyotype 8.
Answer 1: Difference b/w wet and dry earwax genes is due to switch of a single DNA unit i.e. single nucleotide polymorphism.
Answer 2: Earwax is important in many ways mainly it is a biological flypaper as it prevents dust and insects from entering the ear.
Answer 3: Genetics have proved that for those who sweat a lot and have armpit odor have wet earwax.
Answer 4: The wet type earwax is dominant one with honey brown or dark brown color while dry one is recessive.
Answer 5: As wet earwax is dominant trait, according to the given scenario the genotype of parent with wet earwax will be "WW" which when crossed with dry earwax parent will have all the offsprings with wet earwax.
Answer:
The universality of genetic code.
Explanation:
The DNA is a molecule made up from 4 different nucleotides (A, T, C or G). The sequence in which these nucleotides are ordered constitute a code that gives a cell instructions to produce a specific protein. This is called the genetic code.
Every three nucleotides code for a specific amino acid. For example, ACG codes for Arginine, CUC codes for Proline, and so on.
The genetic code is universal. This means that in all living organisms, a particular sequence of three nucleotides will code for the same amino acid. This property guarantees that the human gene that codes for human insulin will also code for human insulin in bacteria.
