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Biology - inheritance
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Biology
Genetics
10th
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20 Terms
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Genome
The entire DNA of an organism
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Gene
A section of a molecule of DNA that codes for a combination of amino acids to make a specific protein
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Homologous chromosomes / autosomes
Chromosomes that have the same genes, in the same location. There are 22 homologous pairs of chromosomes in human nuclei.
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Alleles
Different forms of the same gene
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Dominant
An allele that is always expressed in the phenotype when present in the genotype (regardless of the other allele)
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Recessive
An allele that is seen in the phenotype only if two copies are present in the genotype and there is no dominant allele present
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Homozygous
This describes a genotype in which the two alleles for a particular characteristic are the same
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Heterozygous
This describes a genotype in which the two alleles for a particular characteristic are different
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Phenotype
The visible characteristics of an organism which occur as a result of its genetics and the environment
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Genotype
The DNA an organism has for a certain characteristic
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Monohybrid inheritance
Inheritance of one gene
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Sex chromosomes
The 23rd pair of chromosomes in humans (not homologous), XX in biological females and XY in biological males
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Chromosome
A structure made of a long length of coiled up DNA
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Codominance
When two alleles are both expressed in the same phenotype (e.g. blood group AB)
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Selection pressure
An environmental factor that affects the chance of survival of an organism
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Mutation
A rare, random change to the sequence of bases in DNA
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Uses of mitosis
Growth, repair, cloning, asexual reproduction
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Use of meiosis
To produce gametes, for sexual reproduction
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Continuous variation
A characteristic that changes gradually over a range of values shows continuous variation. Examples include height, weight and handspan.
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Discontinuous variation
A characteristic with a limited number of possible values shows discontinuous variation. Examples include eye colour, blood group and biological sex.