An individual who is heterozygous for a recessively inherited disorder and who therefore does not show symptoms of that disorder
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Codon
A three-nucleotide sequence in mRna that specifies a particular amino acid or polypeptide termination signal; basic unit of the genetic code
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Codominant
Expressing two different alleles of a gene in a heterozygote
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Dihybrid cross
A mating of individuals differing at two genetic loci
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DNA
Deoxyribonucleic acid; The genetic material that organisms inherit from their parents
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Dominant Allele
In a heterozygote, the allele that determines the phenotype with respect to a particular gene
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Exons
In eukaryotes, a coding portion of a gene
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F1 Generation
The offspring of two parental individuals (stands for first filial)
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F2 Generation
The offspring of the F1 generation (stands for second filial)
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Genetics
The scientific study of heredity
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Genotype
The genetic makeup of an organism
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Heredity
The transmission of traits from one generation to the next
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Heterozygous
Having two different alleles for a given gene
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Homozygous
Having two identical alleles for a given gene
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Hybrid
The offspring of parents of two different species or of two different varieties of one species
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Incomplete Dominance
A type of inheritance in which the phenotype of a heterozygote is intermediate between the phenotypes of the two types of homozygotes
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Introns
In eukaryotes, a nonexpressed portion of a gene that is excised from the RNA transcript
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Law of independent assortment
A general rule of inheritance, first proposed by Gregor Mendel, that states that when gametes form during meiosis, each pair of alleles for a particular character segregate independently of each other pair
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Law of segregation
A general rule of inheritance, first proposed by Gregor Mendel, that states that the two alleles in a pair segregate into different gametes during meiosis
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Linked genes
Genes located close enough together on a chromosome that they are usually inherited together
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Locus
The particular site where a gene is found on a chromosome
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Messenger RNA (mRNA)
The type of ribonucleic acid that encodes genetic information from DNA and conveys it to ribosomes, where the information is translated into amino acid sequences
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Monohybrid Cross
A mating of individuals differing at one genetic locus
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Mutagen
A chemical or physical agent that interacts with DNA and causes a mutation
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Mutation
A change in the nucleotide sequence of DNA; a major source of genetic diversity
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Nucleotide
An organic monomer consisting of a five-carbon sugar covalently bonded to a nitrogenous base and a phosphate group (building blocks of nucleic acids)
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Pedigree
A family tree representing the occurrence of heritable traits in parents and offspring across a number of generations
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P generation
The parent individuals from which offspring are derived in studies of inheritance. P stands for parental
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Phenotype
The expressed traits of an organism
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Pleiotropy
The control of more that one phenotypic character by a single gene
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Polygenic inheritance
The additive effect of two or more genes on a single phenotypic characteristic
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Punnett Square
A diagram used in the study of inheritance to show the results of random fertilization
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Recessive Allele
In Heterozygotes, the allele that has no noticeable effect on the phenotype
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sex-linked gene
A gene located on a sex chromosome
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Trait
A variant of a character found within a population, such as purple flowers in pea plants
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Transcription
The synthesis of RNA on a DNA Template
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Translation
The synthesis of a polypeptide using the genetic information encoded in an mRNA Molecule