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Thalassemia is carried on chromosome 11 and chromosome 16, depending on the type. The alpha-thalassemia gene is located on chromosome 16, while the beta-thalassemia gene is found on chromosome 11. Mutations in these genes affect the production of hemoglobin, leading to the various forms of thalassemia.
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What is the chromosome carried only by the sperm called?
The chromosome carried only by the sperm is called the Y chromosome, which determines the male gender when combined with the X chromosome from the egg during fertilization.
What is the name of genes that are carried on the same chromosome?
Genes that are located on the same chromosome are called linked genes. These genes tend to be inherited together during cell division because they are physically close to each other on the same chromosome.
What chromosome is affected by meckel syndrome?
Meckel Syndrome (type 1)is an autosomal recessive trait carried on chromosome 17.
What mutations does beta-thalassemia have on DNA?
Beta-thalassemia is typically caused by mutations in the HBB gene located on chromosome 11. Common mutations include point mutations, deletions, or insertions in the HBB gene, leading to reduced or absent production of beta-globin chains in hemoglobin. These mutations disrupt the normal structure and function of hemoglobin, resulting in anemia and other symptoms associated with beta-thalassemia.
What role do DNA and chromosomes play in heredity?
according to the chromosome theory of inheritance,genes are carried from parents to their offspring on chromosomes.
What is the chromosome carried only by the sperm called?
The chromosome carried only by the sperm is called the Y chromosome, which determines the male gender when combined with the X chromosome from the egg during fertilization.
What condition is carried on a chromosome other then the sex chromosome?
The gene that causes cystic fibrosis is located on chromosome 7, which is an autosome, not a sex chromosome.
What describes allele that causes color blindness?
It is carried on the X chromosomeIt is carried on the X chromosome
What describes the allels that causes color blindness?
It is carried on the X chromosomeIt is carried on the X chromosome
What kind of conditions is carried on a chromosome other than the sex chromosome?
This would be just a genetic or inherited condition.
What is the name of genes that are carried on the same chromosome?
Genes that are located on the same chromosome are called linked genes. These genes tend to be inherited together during cell division because they are physically close to each other on the same chromosome.
Genetic information is carried from the chromosome to the ribosome by the?
Messenger RNA.
Why is hemophilia considered to be a sex-linked?
It is carried on the X chromosome.
Why is hemophilia considered to be a sex trait?
It is carried on the X chromosome.
What chromosome is affected by meckel syndrome?
Meckel Syndrome (type 1)is an autosomal recessive trait carried on chromosome 17.
What traits like colorblindness that are carried on the x chromosome are what genes?
Traits like colorblindness, hemophilia, and Duchenne muscular dystrophy are carried on the X chromosome. These traits are caused by mutations in specific genes located on the X chromosome, such as the OPN1LW and OPN1MW genes for colorblindness and the F8 and F9 genes for hemophilia.
What mutations does beta-thalassemia have on DNA?
Beta-thalassemia is typically caused by mutations in the HBB gene located on chromosome 11. Common mutations include point mutations, deletions, or insertions in the HBB gene, leading to reduced or absent production of beta-globin chains in hemoglobin. These mutations disrupt the normal structure and function of hemoglobin, resulting in anemia and other symptoms associated with beta-thalassemia.
