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2 identical alleles for a given gene |
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2 different alleles for a given gene |
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In a heterozygote the allele that decides the phenotype |
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In a heterozygote the allele that has no visible effect on the phenotype |
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Type of inheritance where the phenotype is in between the 2 alleles of a heterozygote |
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The expression of 2 different alleles in a heterozygote |
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The parents differ in one characteristic |
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2 Characteristics are different |
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Discreet unit of hereditary information |
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Alternative form of a gene |
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Genetic makeup of an organism |
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Expressed traits of an organism |
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Mating of an individual genotype and an individual that is homozygous recessive for same characteristic |
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2 chromosomes that pair up in a diploid organism |
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Studying the family tree for the occurrence of inheritable traits |
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Chromosome not directly involved in determining the sex of an organism |
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Chromosome that determines the sex |
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Trait that is tied to a sex chromosome |
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Individual that is heterozygous, doesn't show phenotype for recessive gene but will pass it on. |
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Control of more than one phenotype by one gene |
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More than one gene controlling a characteristic |
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Genes located close together that are inherited together |
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First to study patterns of inheritance without DNA |
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Mendel's law of segregation |
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Sperm/Eggs only carry one allele for a characteristic |
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Law of independent assortment |
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Inheritance of one characteristic has no effect on another |
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Only one allele is expressed |
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Phenotype is mixed between the 2 parents |
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Expression of 2 different genes in a heterozygote |
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Polymer consisting of many nucleotides |
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5 carbon sugar bonded with a phosphate and a nitrogen base |
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Set of rules that gives the information to the protein |
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3 bases that match with the an amino acid |
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Change in the genetic code |
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Base substitution mutation |
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one base is substituted for another |
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Base insertion or deletion mutation |
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A base goes away or a new one is added |
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Thing that causes a mutation |
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Genes in a sack that can infect cells |
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Structure of the DNA molecule |
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Sugar phosphate backbone with bases. 2 strand joined together at bases to form a double helix |
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Why is base complementarity important? |
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It enables the DNA to replicate and for RNA to be transcribed |
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RNA polymerase starts at a promoter then works it's way down the DNA, first unzipping the section then matching up the bases. It stops at a terminator |
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mRNA meets up with tRNA in a ribosome. Then an anti Codon in the tRNA matches with a Codon in mRNA. Then the tRNA finds the corresponding amino acid |
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2 ways mutations are harmful |
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Change the amino acid order making a protein useless
Cause cancer |
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2 ways mutations are helpful |
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Creates diversity
Enables researchers to create different alleles |
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