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Science - Genes

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Term
Definition
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.  
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Karyotype   The number and visual appearance of the chromosomes in the cell nuclei of an organism or species  
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Amino Acid Sequence   The order of which amino acid residues, connected by peptide bonds, lie in the chain in peptides and proteins  
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Genotype   The genetic constitution of an individual organism  
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Phenotype   The set of observable characteristics of an individual resulting from the interaction of its genotype with the environment  
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Genetic Mutation   Permanent alteration in the DNA sequence makes up a gene, such that the sequence differs from what is found in most people. Mutations range in size.  
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Mitosis   A type of cell division that results in two daughter cells each having the same number and kind of chromosomes as the parent nucleus, typical of ordinary tissue growth.  
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Meiosis   A type of cell division that results in four daughter cells each with half the number of chromosomes of the parent cell, as in the in the production of gametes and plant spores.  
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Dominant   An allele can be recessive or dominant  
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Recessive   Only shows if the individual has two copies of the recessive allele - eg. allele from blue eyes is recessive  
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Co - Dominant   When two alleles for a trait are equally expressed with neither being recessive or dominant  
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Alleles   Forms of genes  
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Punnet Square   Diagram used to predict an outcome of a particular cross or breeding experiment.  
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Monophybrid Cross   Mating between two individuals who have different alleles  
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Autosomal   One of several ways a trait, disorder or diseased can be passed down though families  
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Mendelian Ratios   Ratio of occurrence of various phenotypes  
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Polygenic Inheritance   Form of inheritance in which a particular trait is produced by the interaction of many genes.  
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