IB Biology Sub-topic D3.2 Definitions

This page contains our IB Biology definitions for sub-topic D3.2. By learning each one of these definitions, you will fully cover the content for IB Biology 'Polygenic inheritance'.
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carrier

An individual that is heterozygous for a genetic disease

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co-dominance

An inherited genotype of two dominant alleles that express a joint phenotype

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continuous variation

The division of characteristics into an infinite number of forms

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discrete variation

The division of characteristics into a finite number of different groups

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dominant allele

An allele who's phenotype is expressed over a recessive allele. Dominant alleles are capitalized (A)

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genotype

The alleles than an organism contains to exhibit a characteristic

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heterozygous

The presence of two different alleles (Aa)

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homozygous

The presence of two of the same alleles (AA or aa)

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linked genes

Genes that are on the same chromosome

locus

A specific position on a chromosome

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mutagen

A substance capable of causing a mutation

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mutation

A random change to the base sequence of a gene

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non-linked genes

Genes that are on different chromosomes

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phenotype

The characteristic physically exhibited by an organism

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polygenic inheritance

The inheritance of multiple genes coding for a single characteristic

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recessive allele

An allele who's phenotype is masked by a dominant allele. Recessive alleles are lowercase (a)

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recombinant

A new combination of linked genes made via recombinatinon during crossing over in prophase I

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segregation

The phenomenon of offspring inheriting one allele from each parent due to the formation of haploid nuclei during meiosis

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sex-linked condition

A condition dependent on the sex of the individual because the allele is present on the X chromosome

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