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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.
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.
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 codon codes for amino acids phenylalanine did scientist find?
There are two codons that code for the amino acid phenylalanine: UUU and UUC.
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.
Who was the inventor of the genetic code?
The genetic code was not invented by a single individual. It is a universal system that describes how DNA sequences are translated into proteins. The code was deciphered over time by many scientists, including Marshall Nirenberg, Har Gobind Khorana, and Severo Ochoa.
