mutated means that when you have a son or a daughter the child doesn't look at all like the parents or you could say. not like any other of its kind
The mutated gene codes for a protein that cause a new trait
protein that is a product of expression of a gene that was mutated.
Someone who has a gene for a recessive genetic disorder but does not exhibit the disorder is referred to as a "carrier." Carriers possess one copy of the mutated gene and one normal gene, which means they can pass the mutated gene to their offspring without showing symptoms of the disorder themselves.
Osteogenesis imperfecta is typically inherited in an autosomal dominant pattern, meaning one copy of the mutated gene is enough to cause the condition. However, in some cases, it can be inherited in an autosomal recessive pattern if both parents are carriers of the mutated gene.
A mutated gene is commonly referred to as a "mutation." Mutations can occur in various forms, such as point mutations, insertions, deletions, or duplications, and they can affect the gene's function. Depending on the nature and impact of the mutation, it may lead to changes in an organism's traits or contribute to genetic disorders.
mutated
A mutated gene is just a gene that doesn't have the correct DNA or alleles.. Depending of the human disorder the gene that is mutated will be different... We use genes throughout our bodies but ALL genes can cause human disorders but there is NO single gene that, when mutated, creates ALL genetic modification...
Most mutations in eukaryotes are recessive because they typically involve changes in a single gene, and the presence of a normal copy of the gene can often mask the effects of the mutated gene. This means that the mutated gene is only expressed when both copies of the gene are mutated, resulting in a recessive trait.
Being heterozygous for a gene means having two different alleles at a particular gene locus. One allele is dominant and the other is recessive. This can result in a combination of traits expressed in an individual.
The mutated gene codes for a protein that cause a new trait
protein that is a product of expression of a gene that was mutated.
The specific sequence of the new mRNA strand produced by a mutated gene will depend on the nature of the mutation. Mutations can cause changes in the coding region of the gene, leading to alterations in the mRNA sequence and potentially affecting the resulting protein or gene function. Further analysis and sequencing of the mutated gene would be required to determine the exact mRNA sequence.
# UV light # carcinogenics # heat # viruses
Huntington's disease is an autosomal dominant genetic disorder, meaning that an individual only needs one copy of the mutated gene from either parent to be affected. Therefore, you cannot be a "carrier" in the traditional sense, as carriers typically refer to autosomal recessive conditions where two copies of a mutated gene are needed to express the disease. However, a person can inherit the mutated gene without showing symptoms until later in life, thus being at risk of developing the disease.
Someone who has a gene for a recessive genetic disorder but does not exhibit the disorder is referred to as a "carrier." Carriers possess one copy of the mutated gene and one normal gene, which means they can pass the mutated gene to their offspring without showing symptoms of the disorder themselves.
The mutated gene codes for a protein that cause a new trait
The mutated gene codes for a protein that cause a new trait