Unit 4 Genetics

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Last updated 3:48 AM on 2/8/26
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38 Terms

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Alleles

different variants of a gene.

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Alleles map to

the same locus on individual chromosomes.

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Allelic

individual has two variants (Gg) of a gene so, the two genes are..

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Non-Allelic

individual has two copies/identical (GG or gg) of a gene so, the two genes are..

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Wild type

the phenotype of the most common form of a species as it occurs in nature.

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Null allele

a mutant allele with the effect of either the absence of gene product or the absence of gene product function due to a loss-of function mutation; most behave as recessive

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e+/e+; +/+

homozygous color

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e/e

homozygous recessive (ebony)

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e+/e; +/e

heterozygous

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R1 and R2

alternative alleles of gene R (flower colors)

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IA, IB, and IO

alternative alleles of gene I (blood types)

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nine of the 100+ alleles of the white locus in Drosophila

w+, w, wa, wcf, wbl, we, wis, wch, wDZL

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incomplete dominance (partial dominance)

neither one of the two contrasting traits is dominant; the phenotype of heterozygous individuals is an intermediate of the two contrasting traits.

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incomplete penetrance

identical known genotypes yield <<100% penetrance: should have color but some are showing the recessive phenotype (no color).

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variable expressivity

Identical known genotypes with an expressivity effect yield range pf phenotypes. 100% penetrance but all have color that are showing in different ways

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Flies that are homozygous for this show different degrees of eye size reduction.

recessive eyeless mutant allele.

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Complete penetrance

Identical known genotypes yield 100% expected phenotype

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Constant expressivity

Identical known genotypes with no expressivity effect yield 100% expected phenotype.

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Penetrance

the frequency with which individuals of a given genotype manifest at least some degree of the trait

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Expressivity

the degree or range in which a phenotype for a given trait is expressed.

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Pleiotropy

a condition in which a single mutation causes multiple phenotypic effects.

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Marfan syndrome

results from an autosomal dominant mutation in fibrillin.

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Fibrillin

a gene that codes for a connective tissue protein present in many tissues in the body.

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Essential Gene

defined as a gene that is necessary for growth and survival, and its absence results in lethality.

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A (agouti) is an..

essential gene.

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A^Y (yellow) is a โ€ฆ.

dominant, pleiotropic, and recessive lethal mutant allele.

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The inheritance of plumage color patterns in mallard ducks depends on the three alleles of the M locus:

M^r: restricted

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M: mallard (wild type)

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m^d: dusky

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M^r (restricted) is dominant over and .

mallard and dusky

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M (mallard) is dominant over _.

dusky

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Codominance

a mode of inheritance in which the phenotypic effects of two allelic genes are fully and simultaneously expressed in heterozygous individuals.

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Type A (IA) dominant

Erythrocytes (red blood cells) with type A surface antigens and plasma with anti-B antibodies

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Type B (IB) dominant

Erythrocytes (red blood cells) with type A surface antigens and plasma with anti-A antibodies

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Type AB (IA and IB are co-dominant)

Erythrocytes (red blood cells) with type A and type B surface antigens and plasma with neither anti-A not anti-B antibodies.

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Type O (Io recessive-null allele)

Erythrocytes (red blood cells) with neither type A not type B surface antigens, but plasma with both anti-A and anti-B antibodies.

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Epistasis

occurs when the effect of one gene masks or modifies the effect of another, non-allelic gene.

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Complementation

occurs when two parents that exhibit a recessive phenotype can yield offspring that exhibit the dominant phenotype for the character.