neither, it is a birth defect
The genotype for a homozygous recessive trait, such as a cleft chin, is represented by two lowercase alleles, typically denoted as "cc." In this case, "c" signifies the recessive allele associated with the cleft chin trait. Therefore, an individual who is homozygous recessive for a cleft chin would have the genotype "cc."
This condition is known as polygenic inheritance. It involves multiple genes contributing to a trait, and the expression of these genes can be influenced by environmental factors. The combination of genetic and environmental influences leads to a wide range of variation in the trait.
A multifactorial trait is a characteristic that is influenced by multiple genetic and environmental factors rather than a single gene. Examples include traits such as height, skin color, and susceptibility to diseases like diabetes. These traits typically show a range of variations within a population due to the interplay of various genes and environmental influences. Understanding multifactorial traits is important in fields like genetics, medicine, and psychology, as they can help explain complex behaviors and health outcomes.
No. There are several genes that can result in clefting with varying degrees of severity. And there are effects from chemicals that can increase the severity.
Multifactorial polygenic threshold theory proposes that complex traits are influenced by both genetic and environmental factors. It suggests that multiple genes contribute to the expression of a trait, and a certain threshold of genetic and environmental factors must be reached to manifest the phenotype. This theory is often used to explain the inheritance of complex traits such as height, intelligence, and susceptibility to diseases.
Huntington's disease is primarily caused by a genetic mutation, specifically an expansion of CAG repeats in the HTT gene located on chromosome 4. This mutation leads to the production of a toxic protein that causes neurodegeneration. While there are some environmental factors that may influence the onset and progression of the disease, it is not considered a multifactorial trait in the same way that conditions like heart disease or diabetes are. Thus, Huntington's disease is fundamentally a chromosomal error rather than a multifactorial condition.
Alzaymrs is ottosomal dominent
Trait that is controlled by many genes and is also influenced by the environment.
Multifactorial trait
The genotype for a homozygous recessive trait, such as a cleft chin, is represented by two lowercase alleles, typically denoted as "cc." In this case, "c" signifies the recessive allele associated with the cleft chin trait. Therefore, an individual who is homozygous recessive for a cleft chin would have the genotype "cc."
About 5-10% of the global population is estimated to have a cleft chin, also known as a "dimple" or "chin cleft." It is a genetic trait caused by a dominant gene.
Both, depending on the genes of the parents. It can also be on genetic and caused by the child's environment in the womb and in very few cases the child's tongue blocks the palate from fully closing
This condition is known as polygenic inheritance. It involves multiple genes contributing to a trait, and the expression of these genes can be influenced by environmental factors. The combination of genetic and environmental influences leads to a wide range of variation in the trait.
The combination Cc has a 50% chance of having a cleft chin trait, while the combination cc will always result in offspring without a cleft chin. Therefore, the ratio of offspring with a cleft chin to offspring without a cleft chin from the cross Cc and cc is 1:1.
Yes, Justin Timberlake has a cleft chin, which is characterized by a noticeable dimple or indentation in the center of the chin. This feature is often considered a distinctive aspect of his appearance and contributes to his recognizable look. Cleft chins are a genetic trait and can vary in prominence among individuals.
All four children in the family will have cleft chins. This is because the parents are homozygous, meaning they have two copies of the gene for cleft chin, and will pass on one copy to each of their children, resulting in all of them inheriting the trait.
One can be born with a cleft chin. Another way one would get a cleft chin, if they wanted it, would be through plastic surgery. A cleft would be bored into the fissure of the chin bone and then one would have a cleft chin.