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A permanent change in a gene or chromosome results in what?
A permanent change in a gene or chromosome results in a mutation. This alteration can affect the structure and function of proteins, potentially leading to changes in an organism's traits or characteristics. Mutations can be beneficial, harmful, or neutral, and they play a crucial role in evolution and genetic diversity. Depending on the nature of the mutation, it can be inherited or occur spontaneously in somatic cells.
What does klinefelters syndrome come from what type of mutation?
Klinefelter syndrome is caused by the presence of an extra X chromosome in males due to a random error in cell division, known as nondisjunction. This results in a chromosomal mutation where males have an additional X chromosome, leading to physical and developmental differences.
Trisomy-21 results from a mutation to the chromosomes in?
Trisomy-21, also known as Down syndrome, results from an extra copy of chromosome 21. Instead of the usual two copies, individuals with Down syndrome have three copies of chromosome 21. This extra genetic material can lead to various physical and cognitive differences.
What is mutation results in death called?
Deviation causes death/mutation of cell, bro.
Will a point mutation cause the cell to make an incomplete polypeptide if the mutation results in a stop codon?
Yes, a point mutation will cause the cell to make an incompelete polypeptide chain that is non-functional, if the mutation results in a stop codon. This type of a mutation is also called as the Nonsense Mutation.
Is angel-man syndrome sex-linked?
No. However, if the maternal copy of chromosome 15 has a mutation on a specific gene, angelman's results. Also, getting two copies of chromosome 15 from the father results in angelman's (Paternal uniparental disomy).
Which chromosomal mutation results in Alagille syndrome?
Alagille syndrome is typically caused by a deletion or mutation in the JAG1 gene located on chromosome 20. This gene provides instructions for making a protein involved in the development of various organs and tissues, including the liver, heart, and eyes.
Type of mutation that causes Trisomy 18?
Trisomy 18 is caused by a type of mutation called nondisjunction, where an error in cell division results in an extra copy of chromosome 18. This leads to the presence of three copies of chromosome 18 in each cell instead of the normal two copies.
What does klinefelters syndrome come from what type of mutation?
Klinefelter syndrome is caused by the presence of an extra X chromosome in males due to a random error in cell division, known as nondisjunction. This results in a chromosomal mutation where males have an additional X chromosome, leading to physical and developmental differences.
Trisomy-21 results from a mutation to the chromosomes in?
Trisomy-21, also known as Down syndrome, results from an extra copy of chromosome 21. Instead of the usual two copies, individuals with Down syndrome have three copies of chromosome 21. This extra genetic material can lead to various physical and cognitive differences.
Trisomy is a mutation that results in a cell having an extra?
A trisomy is a condition in which a person has three copies of a chromosome instead of the usual two copies. A person can have full trisomy (three copies in every cell) or mosaic trisomy (three copies in some cells but not all).
What is mutation results in death called?
Deviation causes death/mutation of cell, bro.
Will a point mutation cause the cell to make an incomplete polypeptide if the mutation results in a stop codon?
Yes, a point mutation will cause the cell to make an incompelete polypeptide chain that is non-functional, if the mutation results in a stop codon. This type of a mutation is also called as the Nonsense Mutation.
How are the three chromosomal aberrations different from each other how are they similar?
The three chromosomal aberrations - deletion, duplication, and inversion - are different in terms of the changes they cause in the chromosome structure. Deletion involves the loss of a segment of the chromosome, duplication results in the presence of extra copies of a segment, and inversion entails the reversal of a segment within the chromosome. These aberrations are similar in that they can all lead to genetic disorders or abnormalities due to the changes in the chromosome structure they cause.
A point mutation will cause the cell to make an incomplete polypeptide if the mutation results in?
codon
Which mutation results in a single missing letter in the genetic code?
frameshift mutation: deletion
What results in formation of new alleles?
mutation
