What is hemophilia?
The F8 gene produces a protein needed for blood clotting. People with hemophilia bleed longer when they are injured because they are unable to form stable blood clots. Mutations in this gene are responsible for more than 90% of hemophilia cases.
chromosome x,hemophilia,blood clots,mutations,protein
- ID: 15949
- Source: DNALC.DNAi
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15950. What causes hemophilia?
The F8 gene produces a protein needed for blood clotting. People with hemophilia bleed longer when they are injured because they are unable to form stable blood clots. Mutations in this gene are responsible for more than 90% of hemophilia cases.
15901. Hemophilia
The F8 gene produces a protein needed for blood clotting.
15967. What is sickle cell?
Mutations in the HBB gene on chromosome 11 can cause sickle cell.
15968. What causes sickle cell?
Mutations in the HBB gene on chromosome 11 can cause sickle cell.
15940. What is color blindness?
The two genes that produce red and green light-sensitive proteins are located on the X chromosome.
15945. What is Fragile X?
The FMR1 gene produces a protein involved in making cellular connections in the brain.
15936. What is beta-thalassemia?
The HBB gene encodes an important blood protein called beta globin. A person with beta-thalassemia carries a mutation in both copies of the HBB gene, completely halting production of the beta globin protein.
15937. What causes beta-thalassemia?
The HBB gene encodes an important blood protein called beta globin. A person with beta-thalassemia carries a mutation in both copies of the HBB gene, completely halting production of the beta globin protein.
15419. X chromosome: gene for color blindness, Matt Ridley
Matt Ridley talks about X chromosome: gene for color blindness.
15946. What causes Fragile X?
The FMR1 gene produces a protein involved in making cellular connections in the brain. If this gene carries many repeats of the nucleotides CGG at one end, it is deactivated. People with this mutation display mental impairments or retardation. Fragile X s