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A collection of vocabulary flashcards covering basic genetics, Mendelian laws, Punnett squares, non-Mendelian inheritance patterns, and human genetic disorders based on the lecture notes.
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Genetics
The scientific study of heredity and hereditary variation.
Heredity
The transmission of traits from one generation to the next.
Gregor Mendel
Known as the "Father of Modern Genetics," he performed crossing experiments using different varieties of garden peas.
Hybridization
Also known as crossing, it is the process of transferring pollen from the stamen of one flower to the carpel of another, such as Mendel's work with purple and white flowers.
Pisum sativum
The scientific name for the garden pea used by Mendel due to its short generation time, variety, and ability to self-pollinate.
Locus
The specific location of a DNA sequence of a gene on a chromosome.
Homozygous
Describes an individual carrying identical alleles for a gene.
Heterozygous
Describes an individual carrying two different alleles of a gene.
Genotype
The particular set of alleles that an individual carries.
Phenotype
The observable traits of an individual, such as flower color.
Dominant Allele
An allele (A) whose effect masks that of a recessive (a) allele paired with it.
Hybrids
Heterozygous offspring resulting from a cross between two homozygous parents.
P Generation
The parental generation.
F1 Generation
The first filial generation, resulting from crossing two parents with contrasting traits.
F2 Generation
The second filial generation resulting from crossing two F1 individuals.
Punnett Square
A grid used to predict the genotypic and phenotypic outcome of a cross.
Monohybrid Cross
A cross between individuals that are heterozygous for the same characteristic, usually starting from a cross between two true-breeding varieties.
Law of Segregation
Mendel's First Law of Genetics stating that the paired unit factors (alleles) separate randomly during the formation of gametes so that each gamete receives one or the other with equal likelihood.
Dihybrid Cross
A cross where the parents are heterozygous for two traits, resulting in a phenotypic inheritance pattern of 9:3:3:1 among the F2 offspring.
Law of Independent Assortment
Mendel's Second Law of Genetics stating that during meiosis, members of a pair of genes on homologous chromosomes get distributed into gametes independently of other gene pairs.
Testcross
A method to determine unknown genotypes by crossing an individual with a dominant phenotype with a homozygous recessive individual.
Codominance
An inheritance pattern where both alleles are expressed, such as in AB blood type where both Carbohydrate A and Carbohydrate B are present on red blood cells.
Incomplete Dominance
An inheritance pattern where the heterozygous phenotype is an intermediate between the two homozygous parents, such as pink flowers resulting from red and white snapdragons.
Polygenic Inheritance
The additive effects of two or more genes on a single phenotypic character, resulting in continuous variation like human skin color, height, and eye color.
Sex-linked Gene
A gene located on a sex chromosome; most are found on the X chromosome, including those for red-green colorblindness and hemophilia.
Hemophilia
A sex-linked recessive trait characterized by a long history in the descendants of Queen Victoria.
Albinism
An autosomal recessive disorder characterized by a lack of pigment in skin, hair, and eyes.
Phenylketonuria (PKU)
An autosomal recessive disorder involving the accumulation of phenylalanine in the blood; products with Aspartame often contain a warning for this condition.
Achondroplasia
An autosomal dominant disorder that results in dwarfism.
Huntington's Disease
An autosomal dominant disorder occurring in middle age characterized by uncontrollable movements and cognitive impairments.