Anatomy & Physiology II: Heredity II

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A set of vocabulary flashcards covering the concepts of inheritance, genetic expression, and hereditary tools based on the lecture notes.

Last updated 1:11 PM on 5/1/26
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16 Terms

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Simple Dominance Inheritance

Reflects the interaction of dominant and recessive alleles where one allele can mask the expression of another.

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Punnett square

A tool used to represent genetic crosses that helps predict possible gene combinations resulting from the mating.

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Dominant allele

Represented by a capital letter, these alleles usually encode functional proteins and are expressed if at least one is present.

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Recessive allele

Represented by a lowercase letter, these alleles often encode defective proteins or no protein at all and are only expressed when the genotype is homozygous.

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Homozygous

A condition where an individual has two identical alleles for a specific gene (e.g., TTTT or tttt).

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Heterozygous

A condition where an individual has two different alleles for a specific gene (e.g., TtTt).

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Huntington’s disease

A condition caused by a delayed-action dominant gene.

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Multiple-Allele Inheritance

Inheritance involving genes that exhibit more than two allele forms, such as the three alleles (IAI^A, IBI^B, ii) that determine ABO blood types.

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Codominant

A type of inheritance where both alleles are expressed if present, such as alleles IAI^A and IBI^B in the ABO blood grouping.

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Sex-Linked Inheritance

Inherited traits determined by genes on the sex chromosomes, where the X chromosome carries over 2500 genes and the Y carries approximately 80 genes.

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Polygenic Inheritance

A pattern of inheritance where several different genes act in concert to produce a trait, resulting in fine-scale phenotypic variation such as skin color, eye color, and height.

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Phenocopies

Environmentally produced phenotypes that mimic conditions caused by genetic mutations.

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Small RNAs

Includes microRNAs (miRNAs) and short interfering RNAs (siRNAs) that bind to mRNAs and cause them to be destroyed or not translated into proteins.

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Extranuclear (Mitochondrial) Inheritance

The transmission of 37 genes found in human mitochondrial DNA (mtDNAmtDNA) which are transmitted by the mother in the cytoplasm of the egg.

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Pedigrees

Charts used to trace a particular genetic trait through several generations to help predict its future occurrence.

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Carrier Recognition

The process of identifying individuals who carry a recessive gene for a disorder using pedigrees and DNA testing.