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Genetics
The study of heredity.
Mendel's Experiments
Foundation for genetics established by Johann Mendel before the identification of chromosomes or genes.
Genes
Basic functional units of heredity that can be replicated, expressed, or mutated. They are carried on chromosomes.
Model system
A system with convenient characteristics used to study a specific biological phenomenon.
Continuous variation
The range of small differences seen among individuals in a characteristic, such as human height.
Discontinuous variation
Variation among individuals where each shows one of two or a very few distinguishable traits.
Alleles
Gene variants that arise by mutation and exist at the same relative locations in homologous chromosomes.
Phenotype
Observable traits expressed by an organism.
Genotype
An organism's underlying genetic makeup, consisting of visible and non-expressed alleles.
Law of dominance
In a heterozygote, one trait will conceal the presence of another trait for the same characteristic.
Monohybrid cross
Fertilization between two true-breeding parents differing by only one characteristic.
Punett square
A tool to determine probabilities by predicting potential outcomes of fertilization events.
Law of segregation
Paired unit factors (genes) segregate equally into gametes, giving offspring equal likelihood of inheriting either factor.
Test cross
Crossing a dominant expressing organism with a homozygous recessive organism for the same characteristic.
Law of independent assortment
Genes do not influence each other regarding the sorting of alleles into gametes; combinations are equally likely.
Dihybrid cross
A cross between two true-breeding parents expressing different traits for two characteristics.
Incomplete dominance
When one allele appears in the phenotype of a heterozygote to the exclusion of another.
Codominance
Both alleles for the same characteristic are simultaneously expressed in a heterozygote.
Linked genes
Genes located physically close on the same chromosome that are inherited together.
Linkage
The tendency of genes located close to each other on the same chromosome to be inherited as a pair.