I believe the answer would be <span>D.) Abnormal</span>
Answer:
Pleiotropy
Explanation:
Pleiotropy is a genetic condition in which a single gene conditions the expression of multiple phenotype. There are different types of pleiotropy depending on the underlining mechanism
- <em>gene pleiotropy</em>
- <em>developmental pleiotropy</em>
- <em>selectional pleiotropy</em>
- <em>antagonistic pleiotropy </em>
<em>Phenylketonuria is a disease characterized by increased level of amino acid phenylalanine in the blood. It caused by mutation to the gene responsible for breaking down phenylalanine in the blood. Elevated level of phenylalanine causes other issues such as mental problems, urine coloration and reduction in skin pigmentation. This is a clear case of pleiotropy.</em>
Answer:
Kepler
<em>Hope</em><em> this</em><em> helps</em><em> </em><em>:</em><em>)</em>
The answer is c in my opinion
Answer:
Not 100% sure- Hope it helps though
Explanation:
Since codons consist of three base pairs, if, for example, only one or two base pairs are deleted, then the way the DNA is read is shifted at the place of the deletion or insertion. After the place of the mutation, ALL of the amino acids that follow will be different.