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If a nucleotide pair were to be removed from a gene, it would cause a frameshift mutation. This would alter the reading frame of the gene, leading to a change in the amino acid sequence of the protein encoded by that gene. This could potentially result in a nonfunctional or altered protein.
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How do you rank the hereditary components nucleotide gamete chromosome and gene from small to large?
nucleotide, gene, chromosome, gamete
What is the change in a gene at a single nucleotide pair?
A mutation.
Gene mutation in which only 1 condon is affected?
A point mutation, specifically a substitution mutation, is when only one nucleotide base is altered in a gene sequence, affecting one codon. This can result in a change in the amino acid encoded by that codon in the mRNA, impacting the protein produced by the gene.
How many nucleotide pairs in human gene?
3.4 billion
How does the nucleotide sequence of a gene compare to that of an entirely different gene?
The nucleotide sequence of one gene can differ significantly from that of an entirely different gene due to variations in the order of the nucleotides. These differences in sequence are the basis for the diversity of genetic information that allows for functional specialization of genes and the expression of different traits. Genes that code for different proteins or perform distinct functions will have distinct nucleotide sequences.
How would the transcription of eukaryotic gene be affected if a replication error changed the nucleotide sequence of the termination signal for that gene?
Extra long proteins are likely to fold improperly and not function correctly. The overall health of the individual would be destroyed.
How do you rank the hereditary components nucleotide gamete chromosome and gene from small to large?
nucleotide, gene, chromosome, gamete
Smallest bit of genetic information?
A gene, because any smaller and it would just be nucleotides.
A mutation that involves a single nucleotide is called a(an)?
A mutation that involves a single nucleotide is called a point mutation. This type of mutation can include substitutions, insertions, or deletions of a single nucleotide in the DNA sequence.
What is the change in a gene at a single nucleotide pair?
A mutation.
A gene consists of how many nucleotide?
hundreds or thousands
Gene mutation in which only 1 condon is affected?
A point mutation, specifically a substitution mutation, is when only one nucleotide base is altered in a gene sequence, affecting one codon. This can result in a change in the amino acid encoded by that codon in the mRNA, impacting the protein produced by the gene.
How many nucleotide pairs in human gene?
3.4 billion
How does the nucleotide sequence of a gene compare to that of an entirely different gene?
The nucleotide sequence of one gene can differ significantly from that of an entirely different gene due to variations in the order of the nucleotides. These differences in sequence are the basis for the diversity of genetic information that allows for functional specialization of genes and the expression of different traits. Genes that code for different proteins or perform distinct functions will have distinct nucleotide sequences.
What are three main types of gene mutations what happens in each gene?
The three main types of gene mutations are point mutations, insertion mutations, and deletion mutations. Point mutations involve changes to a single nucleotide base. Insertion mutations involve the addition of extra nucleotide bases. Deletion mutations involve the removal of nucleotide bases in a gene sequence.
Which of the following statements does not accurately describe DNA?
A change in the nucleotide sequence of a gene
What is a gene segment called in a DNA molecule?
Nucleotidehttp://en.wikipedia.org/wiki/Nucleotide
