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SLS Bio 11 Genetics CP

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Term
Definition
Allele   Different form of a gene, they occur during the same locus on homologous chromosomes.  
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Autosome   Any type of chromosomes except for the sex chromosomes.  
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Codominance   A pattern of inheritance when both alleles of a gene are equally expressed.  
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Dihybrid   One individual that is heterozygous for two traits; it shows the phenotype by the dominant alleles but carries the recessive alleles.  
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Dominant allele   An allele that gets its phenotypic effect in the heterozygote; it receives the expression of the recessive allele.  
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Genotype   Genes of a individual of a particular train or trait, designated often by letters such as BB or Aa.  
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Heterozygous   Having two different alleles for a given trait.  
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Homozygous   Having identical alleles for a given trait, free breeding.  
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Monohybrid   Individual for one trait that is heterozygous; the phenotype of the dominant allele but carries the recessive allele.  
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Multiple allele   Inheritance pattern where there are more than two alleles for a particular trait; every individual only has two possible alleles.  
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Phenotype   Different appearance of the organism caused by genotype and environmental influences.  
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Punnet square   Gridlike device that is used to calculate the results of simple genetic crosses.  
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Recessive allele   Hereditary factor that show itself as a phenotype only when it is the genotype.  
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Sex chromosomes   Chromosomes that determine the sex of a human being.  
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Sex-linked trait   Allele that happens on the sex chromosomes but can sometimes control a trait that has nothing to do with sexual characteristics.  
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Test cross   The cross between an individual with dominant phenotype and an individual that has a recessive phenotype. The phenotypic ratio after indicates if the dominant phenotype is homozygous or heterozygous.  
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Apoptosis   Cells that are no longer needed or are a threat to the organism are destroyed.  
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Cell Cycle   Series of events that take place in a cell leading to its division and replication that produces two daughter cells in prokaryotes.  
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Centromere   Part of a chromosome that links sister chromatids during mitosis attaches to spindle fibers.  
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Chromatin   DNA and proteins that forms chromosomes within the nucleus of eukaryotic cells.  
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Chromosomes   Thread-like structures located inside the nucleus, formed of protein and a single molecule.  
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Crossing-over   Process where homologous chromosomes pair up with each other and exchange different segments of their genetic material to form recombined chromosomes.  
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Cytokinesis   Process of cell division, which divides the cytoplasm.  
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Diploid (2n) chromosome number   Cell or organism that has paired chromosomes, one from each parent.  
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Gamete   Organism's reproductive cells they are also called a sex cells.  
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Haploid (n) chromosome number   Half the usual number of chromosomes.  
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Homologous chromosomes   Similar but not identical, each carries the same genes.  
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Meiosis   Process to convert a diploid cell to a haploid gamete.  
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Mitosis   Cell cycle in which chromosomes in a cell nucleus are separated into two identical sets of chromosomes.  
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Nondisjunction   Failure of homologous chromosomes or sister chromatids to separate properly during cell division.  
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Somatic cell   Any cell of the body except sperm and egg cells.  
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Synapsis   Pairing of two homologous chromosomes that occurs during meiosis.  
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