The Y Chromosome.
Chromosome 5.The gene is known as TERT (or, in humans, hTERT) and is the most distal gene on the short arm of chromosome 5 (5p). Its location is 5p15.33. For more detail, see the link below.
He will pass this harmful sex-linked gene on to his daughters. Sons will inherit their Y chromosome from their father, not his X chromosome.
A woman carrying a gene for hemophilia is typically a carrier with one X chromosome carrying the hemophilia gene and one X chromosome carrying the normal gene. When she is mated with a normal male who has one X chromosome and one Y chromosome, there is a 50% chance that the son will inherit the X chromosome carrying the hemophilia gene from the mother. Since males have only one X chromosome, if they inherit the hemophilia gene, they will express the disorder.
XX = female. XY= male because the Y chromosome has SRY gene (Sex-deterimining Region Y). The SRY gene in mammals makes the body produce testis which makes testosterone making the foetus male. For more information, please see the related link below.
When a gene is linked to a chromosome, it means that the gene is physically located on that chromosome. This means that the gene is inherited along with the chromosome it is located on, and may be inherited together with other nearby genes on the same chromosome.
The defective gene in Hurler syndrome is located on chromosome 4. This gene carries instructions for making an enzyme called alpha-L-iduronidase, which is essential for breaking down certain complex molecules in the body. When this gene is mutated, the enzyme is deficient, leading to the accumulation of harmful substances in the cells.
False. A mutation refers to a change in the DNA sequence of a gene or chromosome, not the specific part of a chromosome that carries information about a trait.
Chromosome 5.The gene is known as TERT (or, in humans, hTERT) and is the most distal gene on the short arm of chromosome 5 (5p). Its location is 5p15.33. For more detail, see the link below.
He will pass this harmful sex-linked gene on to his daughters. Sons will inherit their Y chromosome from their father, not his X chromosome.
no. what you described is a gene. a mutation is a change in the DNA which can sometimes change a gene
A gene is a part of the chromosome what is linked to your DNA it carries the proteins which make you, you! Factors that control traits.
A woman carrying a gene for hemophilia is typically a carrier with one X chromosome carrying the hemophilia gene and one X chromosome carrying the normal gene. When she is mated with a normal male who has one X chromosome and one Y chromosome, there is a 50% chance that the son will inherit the X chromosome carrying the hemophilia gene from the mother. Since males have only one X chromosome, if they inherit the hemophilia gene, they will express the disorder.
nucleus → chromosome → gene
In cases where a defective gene is located on the X chromosome, a female can inherit the gene from either parent. If the mother carries one defective X chromosome, she can pass it on to her daughter. Similarly, if the father has the defective gene on his single X chromosome, he will pass it to all his daughters, as they inherit his X chromosome. Therefore, females can receive the defective gene from both maternal and paternal sources.
Smallest to largest: Gene (a place on a chromosome); chromosome (there are 46 in human cells); and DNA (because it accounts for all the genetic material in a cell).
XX = female. XY= male because the Y chromosome has SRY gene (Sex-deterimining Region Y). The SRY gene in mammals makes the body produce testis which makes testosterone making the foetus male. For more information, please see the related link below.
The Y chromosome is the chromosome that determines male sex. It carries the SRY gene that triggers the development of male characteristics during embryogenesis.