Autism
Dwarfism
Sickle cell disease is a mutation in the gene that codes for hemoglobin, which causes the hemoglobin and the cell to become elongated and look like a sickle rather than its normal disc shape.
Huntington's disease is passed to offspring because it is a genetic mutation. Chromosome number four contains a gene called IT15 that codes for the amino acid in glutamine in the protein huntingtin. The nucleotide triplet that codes for this (CAG) usually repeats 11-34 times, but in a Huntington's gene it repeats 37-121 times. This "stutter" can lengthen when passed on through heredity, therefore increasing the chance that a person will have the disease.
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Hungtington's disease is a dominant mutation in the gene that codes for the protein 'Huntington' It only affects a single gene, the remainder of the chromosome is unaffected and therefore it is not a chromosomal abnormality
Both a silent and missense mutation is a change in one nucleotide. However, a silent mutation still codes for the same amino acid, but a missense mutation codes for a different amino acid. This means that a silent mutation will have no affect on the resulting protein, but a missense mutation will. Still, it is not guaranteed that a a missense mutation will result in a disfunction of created protein, as long as it is not occurring in the activation site.
The syndrome is caused by a defect (mutation) in a specific gene called the WAS gene that normally codes for the protein named Wiskott-Aldrich Syndrome Protein (WASP).
Yes, as one base change can influence the protein structure that it codes for. For example patients suffering from Sickle Cell Anaemia.
A Missense Mutation.It is a point mutation where the mutations alters the base sequence without changing the resulting function of the subsequent protein. This is usually when the mutation does not change the amino acid which the codon codes for.
The mutated gene codes for a protein that cause a new trait
The mutated gene codes for a protein that cause a new trait
A point mutation causes a change in the amino acid sequence creating a new type of protein. The mutations are categorized functionally as nonsense, missense and silent mutations.
The mutated gene codes for a protein that cause a new trait