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Gene
Section of DNA that carries a code to make a protein
Genome
The complete set of DNA contained within an organisms chromosomes
Alleles
Alternative form of a gene
Chromosomes
Each molecule of DNA is coiled tightly around histone proteins and packaged into thread-like structures
Homologous chromosomes
Each set of 23 chromosomes within a human nucleus
Karyotype
Visual representation of individuals entire genome organised into pairs
Aneuploidy
Incorrect number of total chromosomes caused by addition or loss of an individual chromosome
Polyploidy
Chromosomal abnormality, organism has more than two sets of each chromosome
Dominant alleles
written as a capital letter
Recessive alleles
written as a lowercase letter
Homozygous
Having the same alleles for same genes
Heterozygous
Having different alleles for the same gene
Genotype
Genetic composition of organism
Phenotype
Observable physical traits, result of gene expression
Complete dominance
Only the dominant allele is expressed
Codominance
Both alleles are fully expressed
Incomplete dominance
Neither allele is fully expressed (allele is blended)
Proportionate heritability
phenotype variance that can be explained by genes in population
Epigenetics
Molecular interactions with DNA that modify expression of genes
DNA methylation
Methyl groups attach to certain nucleotides and alter level of gene expression, reducing transcription
Histone modification
Histone modifying enzymes modify how tightly a DNA molecule is wrapped around the histone
Importance of Epigenetics
Help control cell differentiation and provide organism mechanism to respond