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An individual who cannot produce phenylalanine would not be viable so I believe what you are asking about is Phenylketonuria which is a genetic disorder found is infants who cannot properly digest phenylalanine (they can manufacture it).
Hospitals test for this disorder in newborns because it is imperative to place babies that test positive on a strict diet to prevent the mental retardation that is associated with the disorder. Early intervention results in a nearly normal life.
What else can I help you with?
Uuu codes for the amino acid phenylalanine in humans and bacteria Theis is due to which property of the Genetic code?
being gay
Is DNA genetic code or genetic blueprint?
DNA is the genetic code
What is secondary genetic code?
The secondary genetic code is the folding of protein.
Is the genetic code is arbitrary?
why genetic code is arbitraryif yesthen prov ur anser
Why doesn't carbohydrates and lipids need a genetic code?
They just dnt need a code!(genetic)
If an individual has no genetics code for phenylalanine what kind of danger does it pose to him?
An individual who cannot produce phenylalanine would not be viable so I believe what you are asking about is Phenylketonuria which is a genetic disorder found is infants who cannot properly digest phenylalanine (they can manufacture it). Hospitals test for this disorder in newborns because it is imperative to place babies that test positive on a strict diet to prevent the mental retardation that is associated with the disorder. Early intervention results in a nearly normal life.
Uuu codes for the amino acid phenylalanine in humans and bacteria Theis is due to which property of the Genetic code?
being gay
Which term to the genetic code of an individual?
genotype
What is a genetic disorder in which the essential digestive enzyme phenylalanine hydroxylase is missing is known as?
A genetic disorder in which the essential digestive enzyme phenylalanine hydroxylase is missing is known as Phenylketonuria (PKU). This leads to a buildup of phenylalanine in the body, which can be toxic to the brain if not managed properly through a restricted diet low in phenylalanine.
Given these codons use the Genetic Code Wheel provided to determine the amino acids. GCG-UUU a. Aspartic acid-leucine-Serine b. Glycina-Cysteine c. Proline-Valine d. Alanine-phenylalanineGiven these c?
The codons GCG and UUU correspond to alanine and phenylalanine, respectively, according to the Genetic Code Wheel. Therefore, the correct answer is d. Alanine-phenylalanine.
What does poly U code for?
phenylalanine
If human genetic defect that results in the failure to metabolize the amino acid phenylalanine is?
Phenylketonuria (PKU) is a genetic disorder that causes a person to be unable to metabolize the amino acid phenylalanine. This leads to a buildup of phenylalanine in the body, which can be harmful to the brain and nervous system if not managed properly. Individuals with PKU require a strict low-phenylalanine diet to prevent complications.
What are the DNA codons for phenylalanine?
There are two codons that code for the amino acid phenylalanine: UUU and UUC.
Other than UUU what is another codon that codes for Phenylalanine (PHE)?
Another codon that codes for Phenylalanine (PHE) is UUC. Both UUU and UUC specify the same amino acid, demonstrating the redundancy in the genetic code known as degenerate codon usage.
What term describes the specific genetic makeup or code for an individual?
nature
How does PKU impact protein synthesis?
PKU (phenylketonuria) is a genetic disorder that affects the enzyme needed to break down the amino acid phenylalanine. Without this enzyme, phenylalanine can build up to harmful levels in the blood and impair protein synthesis. The excess phenylalanine can also lead to decreased levels of other amino acids, affecting overall protein production in the body.
What is penylketonuria?
Phenylketonuria (PKU) is a rare genetic disorder in which the body cannot process phenylalanine properly. This leads to a buildup of phenylalanine in the body, which can be toxic to the brain and cause intellectual disabilities if not managed through a low-phenylalanine diet. PKU is typically identified through newborn screening tests and requires lifelong dietary management.
