When the gene is dominant and the traits are autosomal.
In genetics, you can either have a dominant allele (A) or a recessive allele (a). Being homozygous means that you have both of either a dominant or a recessive allele (ie you are either AA or aa). If the trait is a recessive trait, then you need to have it be homozygous recessive in order to express that trait. Hope this was helpful! :-)
A homozygous dominant trait occurs when an individual inherits two identical dominant alleles for a specific gene. The trait is fully expressed, as dominance masks recessive alleles. For example, in pea plants, homozygous dominant (RR) for flower color results in purple flowers, visibly demonstrating the dominant trait without variation. visit our website: www. chocolatekidsplayschool.org/madambakkam/
Marfan syndrome is not sex linked. It is autosomal dominant and found equally in all genders and ethnicities.
The tufted head trait in ducks is typically a dominant gene. This means that if a duck carries the tufted head gene, it is likely to express the trait, even if it also carries a recessive gene for a non-tufted head.
An animal with two homozygous dominant alleles (HH) would exhibit the dominant trait associated with that gene, assuming it is a simple Mendelian trait. This means the animal would show the dominant phenotype controlled by the gene in question.
It is an autosomal recessive trait.
There is two answers, it is autosomal dominant showing incomplete dominace
Huntington's Disease is an Autosomal Dominant Trait, meaning that only one parent needs to pass the disease for the offspring to inherit it.
Alzaymrs is ottosomal dominent
The PTC trait is autosomal dominant so an individual with the trait could be homozygous dominant or heterozygous.
Sickle cell anemia is an autosomal recessive disease. Carriers have sickle cell trait, which confers resistance to malaria.
Down syndrome is neither dominant nor recessive. Actually, it is considered to be an "autosomal" trait. This occurs when there is damage to the chromosome.
0. Unless there is a germline mosaicism or sporadic mutation in the fertilized embryo.
Autosomal dominant traits typically do not skip generations because affected individuals usually have a 50% chance of passing the trait on to their offspring. However, the trait may appear to skip generations if carriers of the trait do not show symptoms or if there is a lack of complete penetrance.
The genotype of a person who is a carrier of an autosomal recessive trait is typically heterozygous, meaning they carry one copy of the recessive allele and one copy of the dominant allele for that trait. This would be represented as Aa, with the lowercase "a" representing the recessive allele.
Autosomal dominant
autosomal dominant