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DNA that codes for a protein which equals a trait -Genetic factor that helps determine a trait |
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One of 2 or more alternative forms of a gene |
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Material Found in Eukaryotic nucleus that consists of DNA and protein |
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is an organized structure of DNA and protein that is found in cells. A chromosome is a single piece of coiled DNA containing many genes, regulatory elements and other nucleotide sequences. |
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Single copy of Chromosome before replication |
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When chromatids have been replicated -same info -> before cells divide in the X (metaphase) |
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Chromosomes that have same type if info but have different forms of the gene |
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genetic phenomenon by which certain genes are expressed in a parent-of-origin-specific manner. It is an inheritance process independent of the classical Mendelian inheritance. Imprinted genes are either expressed only from the allele inherited from the mother |
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Found when one allele is not dominant over another allele at a locus. Phenotype of the heterozygote is different from the phenotypes of either homozygotes |
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Genes that kill the individual before birth. Heterozygote Recessive individuals don't exist in the population |
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Genes that eventually kill an individual after a long portion of life. Ex. Huntington's Disease |
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Can observe both gene products directly. Ex. ABO Bloodgroups |
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Gene is responsible for more than one seemingly unrelated phenotypic event. Ex. Dwarfism and low muscle tone |
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Interaction among several loci |
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Single Recessive Epistasis |
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Recessive trait at one locus masks the effect of the second locus |
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Single Dominant Epistasis |
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Dominant trait at one locus masks the effect of the second locus |
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Duplicate Recessive Epistasis |
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Recessive trait at either locus masks the expression of the dominant phenotype at the other locus |
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Duplicate Genes with Cumulative Effect |
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Duplicate effects from two loci |
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A type of cytoplasmic inheritance where the maternal cell is infected by a bacterial cell where the infection is passed onto cells offspring. Rare in high level organisms |
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Type of Cytoplasmic Inheritance where organelles (mitochondria and chloroplasts) are inherited strictly from maternal cell |
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Females have the characteristic but not expressed |
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is a mode of inheritance in which a mutation in a gene on the X chromosome causes the phenotype to be expressed (1) in males (who are necessarily hemizygous for the gene mutation because they have only one X chromosome) and (2) in females who are homozygous for the gene mutation |
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An Father with this gene will pass on the disorder to all of his daughters |
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A pattern of inheritance in which an affected individual has one copy of a mutant gene and one normal gene on a pair of autosomal chromosomes. 50/50 chance of passing it on |
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A genetic condition that appears only in individuals who have received two copies of an autosomal gene, one copy from each parent. The gene is on an autosome, a nonsex chromosome. The parents are carriers who have only one copy of the gene and do not exhibit the trait because the gene is recessive to its normal counterpart gene. |
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