In humans,the gene responsible for Phenylketo | vedclass

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(B) The phenomenon where a single gene influences multiple,seemingly unrelated phenotypic traits is known as $Pleiotropy$.In the case of $Phenylketonu

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Pleiotropic gene

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(B) The phenomenon where a single gene influences multiple,seemingly unrelated phenotypic traits is known as $Pleiotropy$.In the case of $Phenylketonuria$ $(PKU)$,the mutation in the gene encoding the enzyme $phenylalanine$ $hydroxylase$ leads to the accumulation of $phenylalanine$.This metabolic defect results in a syndrome characterized by various symptoms,including mental retardation,reduction in hair and skin pigmentation,and other physiological abnormalities.Since one gene is responsible for this wide range of phenotypic effects,it is classified as a $Pleiotropic$ gene.

In humans,the gene responsible for Phenylketonuria produces multiple phenotypic expressions,collectively known as a syndrome. This gene causes mental retardation,broad incisor teeth,skin pigmentation,and excessive sweating. What is this type of gene called?

Similar Questions

Which one of the following is an example of pleiotropy?

Which of the following is associated with multiple phenotypes?

$A$ : Myotonic dystrophy is caused by a recessive mutant pleiotropic gene.
$R$ : Gene mutation leads to more synthesis of fibrillin proteins.

The gene disorder phenylketonuria is an example of

Define the term: Pleiotropy.

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