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QuestionAnswer
alleles An allele is a different version of the same gene that helps determine a trait, like eye color or blood type.
autosomes Autosomes are the chromosomes that carry most of your genes and are not involved in determining your sex.
centromere A centromere is the part of a chromosome that holds the two sister chromatids together and helps them separate during cell division.
chromatid A chromatid is one of the two identical halves of a duplicated chromosome that are joined together at the centromere.
chromosome A chromosome is a tightly packed structure made of DNA that carries genes and instructions for how the body grows and works.
deletion mutation A deletion mutation is a change in DNA where a piece of a chromosome or gene is missing.
DNA DNA is the molecule that carries genetic instructions that tell cells how to grow, develop, and function.
DNA primer A DNA primer is a short piece of DNA that starts the process of copying DNA by giving enzymes a place to begin.
dominant allele A dominant allele is a version of a gene that shows its trait even if only one copy is present.
eukaryotic Eukaryotic describes cells that have a nucleus and other membrane-bound organelles.
familial hypercholesterolemia Familial hypercholesterolemia is an inherited condition that causes very high cholesterol levels, which can increase the risk of heart problems.
frameshift mutation A frameshift mutation is a change in DNA where a letter (base) is added or deleted, shifting how the genetic code is read and usually changing the protein made.
gene A gene is a section of DNA that gives instructions for making a specific trait or protein in your body.
genome A genome is all of the DNA in an organism, including all of its genes.
genotype A genotype is the combination of alleles a person has for a specific gene.
gel electrophoresis Gel electrophoresis is a lab method that separates DNA, RNA, or proteins by size using an electric current.
heterozygous Heterozygous means having two different alleles for the same gene.
homozygous Homozygous means having two identical alleles for the same gene.
homologous chromosomes Homologous chromosomes are pairs of chromosomes that have the same size, shape, and genes, with one coming from each parent.
insertion mutation An insertion mutation is a change in DNA where extra DNA bases are added, which can affect how a protein is made.
karyotype A karyotype is a picture of all the chromosomes in a cell, arranged by size and type.
messenger RNA (mRNA) Messenger RNA (mRNA) is a type of RNA that carries instructions from DNA to make proteins.
mitosis Mitosis is the process where a cell divides to make two identical cells with the same number of chromosomes.
mutation A mutation is a change in DNA that can affect how a gene works or how a trait develops.
nondisjunction Nondisjunction is when chromosomes don’t separate properly during cell division, which can lead to extra or missing chromosomes.
nucleotides Nucleotides are the building blocks of DNA and RNA, made of a sugar, a phosphate, and a base.
pedigree A pedigree is a family tree that shows how a trait or disease is passed down through generations.
point mutation A point mutation is a change in a single DNA base that can affect a gene.
polymerase chain reaction A polymerase chain reaction (PCR) is a lab method that makes many copies of a specific DNA segment.
protein A protein is a molecule made of amino acids that helps your body build tissues, carry out chemical reactions, and do many important jobs.
protein synthesis Protein synthesis is the process where cells make proteins using instructions from DNA.
punnett square A Punnett square is a chart that shows all the possible genetic combinations from two parents.
recessive allele A recessive allele is a version of a gene that only shows its trait if both copies are the same.
restriction enzyme A restriction enzyme is a protein that cuts DNA at specific sequences.
ribonucleic acid (RNA) Ribonucleic acid (RNA) is a molecule that helps carry instructions from DNA and makes proteins in cells.
sex chromosomes Sex chromosomes are the chromosomes that determine whether a person is male or female.
silent mutation A silent mutation is a change in DNA that does not change the protein made.
Created by: user-2003220
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