Genetics and Non-Mendelian Inheritance Vocabulary

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30 vocabulary flashcards covering basic genetics rules, recombination, trait types, non-Mendelian inheritance, and organellar genetics.

Last updated 12:35 AM on 8/28/26
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30 Terms

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Product rule

Rule stating that the probability of two independent events occurring together is equal to the product of their individual probabilities.

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Sum rule

Rule stating that the probability of occurrence of any one of two mutually exclusive events is the sum of their individual probabilities.

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Homologous recombination

A type of genetic recombination in which nucleotide sequences are exchanged between two similar or identical molecules of DNA.

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Crossing over

The process during meiosis where homologous chromosomes exchange segments of genetic material.

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Quantitative Trait

A phenotypic characteristic that exhibits continuous variation across a spectrum and is influenced by multiple genetic and environmental factors.

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Quantitative Traits

Measurable phenotypes that show continuous variation rather than discrete categories.

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Quantitative Trait Loci

Specific regions of DNA containing genes that contribute to the phenotypic variation of a quantitative trait.

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Quantitative Trait Locus

A single chromosomal region or segment of DNA linked to variation in a quantitative trait.

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Complex Trait

A trait whose phenotypic expression is governed by multiple genetic and environmental factors rather than a single gene.

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Complex Traits

Phenotypes that do not exhibit simple Mendelian inheritance due to polygenic and environmental contributions.

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Non-mendelian Inheritance patterns

Patterns of inheritance that do not segregate according to Mendel's traditional laws of inheritance.

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Non-mendelian Inheritance

The transmission of traits that fail to conform to classical Mendelian principles.

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Epistasis

An interaction between genes where the phenotypic expression of one gene masks or modifies the allele at another locus.

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Epistatic interaction

A genetic relationship in which the phenotypic effect of one gene depends on the presence of modifier genes at another locus.

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Multiple allelism

The condition of having three or more alternative allele forms of a gene present within a population.

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Multiple alleles

Three or more variant forms of a gene that exist at a single locus within a population.

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Codominance

A pattern of inheritance in which two different alleles at a locus are fully and equally expressed in the phenotype.

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Codominant expression

Simultaneous and equal phenotypic expression of both alleles in a heterozygous individual.

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Uniparental inheritance

An inheritance pattern where extranuclear or organellar genes are inherited strictly from one parent.

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Maternal inheritance

A type of uniparental inheritance in which progeny inherit organelles and their genetic material solely from the female parent.

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Mitochondria

Cellular organelles responsible for energy production that contain their own non-nuclear DNA genome.

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Mitochondrial DNA

The circular DNA molecule present inside mitochondria that encodes specific organelle components.

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Chloroplast

A plant cell organelle that carries out photosynthesis and contains its own distinct DNA genome.

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Chloroplast DNA

The circular genetic material found within chloroplasts that encodes photosynthetic and organelle functions.

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mtDNA

Abbreviation for mitochondrial DNA, which is inherited maternally in many eukaryotic organisms.

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cpDNA

Abbreviation for chloroplast DNA, which contains genes essential for chloroplast function and photosynthesis.

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cytoplasmic segregation

The random distribution of cytoplasmically inherited organelles and their genomes to daughter cells during division.

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Cytoplasmic Inheritance

Transmission of genetic information through cytoplasmically located organelles like mitochondria and chloroplasts.

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Organellar Inheritance

Inheritance of genes located in cytoplasmic organelles rather than the cell nucleus.

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Organellar DNA

Extranuclear genetic material contained within organelles such as mitochondria (mtDNA) or chloroplasts (cpDNA).