Mendelian Genetics and Gene Concepts
Terms in this set (21)
The idea that genetic material from two parents blends together in offspring, producing a uniform mixture.
Genes retain their separate identities through generations and can be separated again, as shown by Mendel's pea plant experiments.
Organisms that produce offspring identical to themselves when self-pollinated or crossed with the same genotype.
Two alleles for a heritable character separate during gamete formation, so each gamete carries only one allele.
An allele that determines the organism's appearance when present, masking the effect of a recessive allele.
An allele that has no noticeable effect on the organism's appearance when paired with a dominant allele.
Genotype is the genetic makeup; phenotype is the observable physical or physiological traits.
Having two identical alleles for a particular gene (e.g., PP or pp).
Having two different alleles for a particular gene (e.g., Pp).
Crossing an organism with a dominant phenotype but unknown genotype with a homozygous recessive individual to determine the unknown genotype.
Alleles of different genes assort independently during gamete formation, applying to genes on different chromosomes or far apart on the same chromosome.
Heterozygous phenotype is intermediate between the two homozygous phenotypes.
Both alleles are fully expressed in heterozygotes, such as in ABO blood groups.
More than two allelic forms of a gene exist in a population, e.g., ABO blood group alleles.
One gene influences multiple phenotypic traits, such as the sickle-cell gene affecting blood and other organs.
One gene affects the expression of another gene, as seen in Labrador coat color inheritance.
Multiple genes contribute to a single phenotypic character, producing quantitative variation, e.g., human height.
Phenotype can be influenced by environmental factors in addition to genotype, leading to multifactorial traits.
A chart used to track inheritance patterns of traits in humans and other organisms across generations.
Disorders that appear only in individuals homozygous for the recessive allele, e.g., cystic fibrosis and albinism.
Disorders caused by dominant alleles, such as achondroplasia and Huntington's disease.