A trait is sex-linked dominant if it appears in every generation and affects both males and females. It is sex-linked recessive if it skips generations, more common in males, and passed from carrier females to affected males. Mendelian inheritance patterns can help determine if a trait is sex-linked dominant or sex-linked recessive.
No, hitchhiker's thumb is not an X-linked trait; it is a result of a genetic variation that is considered to be an autosomal trait. This means it can be inherited from either parent, regardless of the sex of the offspring. The trait is associated with the flexibility of the thumb joint, and its inheritance pattern follows a simple Mendelian trait pattern rather than being linked to the sex chromosomes.
Chromosomes do not have a sex/gender but determine it. In humans, females have two X chromosomes (XX) and males have an X and a Y chromosome (XY).
DiGeorge syndrome is not caused by a single gene mutation, but rather by a deletion of a portion of chromosome 22. It is not inherited in a simple Mendelian pattern like dominant autosomal or sex-linked traits.
Sex linkage refers to genes located on the sex chromosomes (X or Y). If a gene controlling a trait is sex-linked, males and females may show different patterns of inheritance. In a Mendelian cross involving a sex-linked gene, the predicted outcome would be influenced by the sex of the offspring and their respective sex chromosomes (XX for females, XY for males). This can result in different inheritance patterns compared to autosomal genes.
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A sex-linked trait is a trait governed by genes on only one of the two sex chromosomes.
A trait is sex-linked dominant if it appears in every generation and affects both males and females. It is sex-linked recessive if it skips generations, more common in males, and passed from carrier females to affected males. Mendelian inheritance patterns can help determine if a trait is sex-linked dominant or sex-linked recessive.
No, hitchhiker's thumb is not an X-linked trait; it is a result of a genetic variation that is considered to be an autosomal trait. This means it can be inherited from either parent, regardless of the sex of the offspring. The trait is associated with the flexibility of the thumb joint, and its inheritance pattern follows a simple Mendelian trait pattern rather than being linked to the sex chromosomes.
Chromosomes do not have a sex/gender but determine it. In humans, females have two X chromosomes (XX) and males have an X and a Y chromosome (XY).
Its a Sex-Linked Trait, so for girls it would be XCxC or XCXcfor it recessivly for boy (They have the greater chance of getting the trait because its only located on the X chromosome) so for boys its XCY for the trait and XcY for it recessivly
No, myopia is not a sex-linked trait. It is a complex trait influenced by both genetic and environmental factors. While genetics play a role, there is no direct link to sex chromosomes determining the development of myopia.
DiGeorge syndrome is not caused by a single gene mutation, but rather by a deletion of a portion of chromosome 22. It is not inherited in a simple Mendelian pattern like dominant autosomal or sex-linked traits.
Sex linkage refers to genes located on the sex chromosomes (X or Y). If a gene controlling a trait is sex-linked, males and females may show different patterns of inheritance. In a Mendelian cross involving a sex-linked gene, the predicted outcome would be influenced by the sex of the offspring and their respective sex chromosomes (XX for females, XY for males). This can result in different inheritance patterns compared to autosomal genes.
A mutation in a sex cell, such as a sperm or egg cell, can be passed on to offspring and affect future generations. In contrast, a mutation in a non-sex cell will only affect the individual and is not passed on to offspring.
A mutation in a sex cell may be passed on to an offspring. A mutation in a somatic (body) cell cannot be passed on to an offspring, but can potentially cause cancer in the person who has the mutation.
A mutation in a sex cell may be passed on to an offspring. A mutation in a somatic (body) cell cannot be passed on to an offspring, but can potentially cause cancer in the person who has the mutation.