This document defines several key genetics terms: gene, which is a sequence of nucleotides that determines the order of monomers in a polypeptide; allele, which are multiple versions of a single gene that an individual inherits from each parent that can be the same (homozygous) or different (heterozygous); chromosome, which carries genetic information in the form of genes; codon, which is a trinucleotide sequence corresponding to an amino acid; gene mutation, which is a permanent alteration in a gene's DNA sequence; and point mutation, which is a change where one base pair is altered within a gene's DNA sequence.
This document defines several key genetics terms: gene, which is a sequence of nucleotides that determines the order of monomers in a polypeptide; allele, which are multiple versions of a single gene that an individual inherits from each parent that can be the same (homozygous) or different (heterozygous); chromosome, which carries genetic information in the form of genes; codon, which is a trinucleotide sequence corresponding to an amino acid; gene mutation, which is a permanent alteration in a gene's DNA sequence; and point mutation, which is a change where one base pair is altered within a gene's DNA sequence.
This document defines several key genetics terms: gene, which is a sequence of nucleotides that determines the order of monomers in a polypeptide; allele, which are multiple versions of a single gene that an individual inherits from each parent that can be the same (homozygous) or different (heterozygous); chromosome, which carries genetic information in the form of genes; codon, which is a trinucleotide sequence corresponding to an amino acid; gene mutation, which is a permanent alteration in a gene's DNA sequence; and point mutation, which is a change where one base pair is altered within a gene's DNA sequence.
Gene - A distinct sequence of nucleotides forming part of a chromosome, the
order of which determines the order of monomers in a polypeptide Allele - Multiple versions of a single gene. (An individual inherits two alleles for each gene, one from each parent. If the two alleles are the same, the individual is homozygous for that gene. If the alleles are different, the individual is heterozygous). Chromosome - A thread-like structure of nucleic acids and protein found in the nucleus of most living cells, carrying genetic information in the form of genes. Codon - A trinucleotide sequence of DNA or RNA that corresponds to a specific amino acid. Gene mutation - A permanent alteration in the DNA sequence that composes a gene. Point mutation - change within a gene in which one base pair in the DNA sequence is altered.