Biology Final-Genetics-AAHS

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graybeal  on May 19, 2012

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Biology Final-Genetics-AAHS

Incomplete dominance
The heterozygous phenotype is somewhere in between the two homozygous parents.
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Incomplete dominance The heterozygous phenotype is somewhere in between the two homozygous parents.
Co-dominance Both alleles contribute to the phenotype. i.e. Speckled or spotted
Dominance Some genes are dominant and will show in the phenotype even if the organism has a dominant and recessive trait.
Recessive Genes that will only show in the phenotype if there are two of them within the organism
Sex-linked Genes Genes that are located on the chromosomes that determine sex in offspring. Males have only one X gene and so the alleles are shown in them.
Punnett Square Used to predict and compare the genetic variations that will result from a cross
Genes Chemical factors that determine traits
Alleles The different results of a gene
Multiple Alleles More than two alleles exist in a population
Polygenic Traits Traits controlled by two or more genes. i.e. AaBb
DNA The material that contains the information that determines inherited characteristics. Made up of Adenine, Thymine, Cytosine, Guanine.
Proteins Nutrients that help build and maintain body tissues. Organic compounds composed mainly of carbon, hydrogen, oxygen, and nitrogen
Codons Consists of three consecutive nucleotides that specify a single amino acid that is to be added to the polypeptide
Meiosis The number of chromosomes per cell is cut in half. Results in the production of four genetically different haploid cells. Prophase, Metaphase, Anaphase, Telophase, Cytokinesis.
Mitosis Results in the production of two genetically identical diploid cells
Prophase Chromosomes pair with their corresponding homologous chromosome to form a tetrad.
Metaphase Spindle fibers attach to the chromosomes
Anaphase Fibers pull the chromosomes toward opposite end of the cell
Telophase and Cytokinesis Nuclear membranes form. The cell separates into two cells (the process starts again)
Karyotype A picture of chromosomes arranged in order
Human chromosomes humans have 46 of these. Two of those chromosomes determine sex. Males have an XY pair and females have an XX pair
Heterozygous Different
Homozygous The same
Haploid A cell that contains a single set of chromosomes and therefore a single set of genes
Diploid A cell that contains both sets of homologous chromosomes
Mutations Changes in genetic material
Point mutations Changes one or a few nucleotides. Occurs at one place in the DNA sequence
Frame-shift Mutations Change every amino acid that follows the point of the mutation
Substitution Changing a single nucleotide to another
Insertion Placing a extra nucleotide into the base sequence
Deletion A single nucleotide is removed from the base sequence
Chromosomal mutations Changes in the number or structure of chromosomes
Mutations effects Most neutral. But dramatic cases may cause harmful disorders
DNA fingerprinting Analyzes sections of DNA that have little or no known function but vary widely to identify people
Pedigree Chart that shows the relationships within a family tree
Blood Types A, B, AB, O.
Humane Genome Project An ongoing effort to analyze the human DNA sequence. Done by "shotgun sequencing"- sequencing small parts then using computers and markers to put the pieces back together.

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