1/45
Looks like no tags are added yet.
Name | Mastery | Learn | Test | Matching | Spaced | Call with Kai | Chat |
|---|
No analytics yet
Send a link to your students to track their progress
Reductionism
Breaking complex things into simpler parts for better understanding.
Mutation
A process that gives rise to mutants.
Forward Genetics
Starting from a pool of random single-gene mutants and finding mutants with phenotypes of interest.
Mendel's Law of Equal Segregation
One allele for each gene is contributed to the gamete, with an equal chance of contributing either allele.
Monohybrid
Heterozygotes for a single gene.
Dihybrid
Heterozygotes for two genes.
Mitosis
A process where a cell divides to produce two identical daughter cells.
Meiosis
A process during the sexual cycle that produces meiocytes that become gametes.
Alleles
Different versions of the same gene.
Haplosufficiency
One functional allele is enough to produce the wild-type phenotype.
Haploinsufficiency
One functional allele is not enough to produce the wild-type phenotype.
Sex Chromosomes
Chromosomes that determine the sex of an organism.
X-linked Recessive
A trait usually present in males, passed from affected males to daughters as carriers.
X-linked Dominant
Affected males pass the condition to all daughters but no sons.
Y-linked Inheritance
Inheritance of genes located on the Y chromosome, such as the SRY gene determining maleness.
Independent Assortment
The heritability of one gene does not affect the heritability of another.
Recombination
The production of new allelic combinations due to independent assortment or crossing over.
Quantitative Trait Loci (QTL)
Genes that control continuous (quantitative) traits.
Maternal Inheritance
Mitochondrial and chloroplast DNA are inherited from the mother.
Linkage
Genes located on the same chromosome that tend to be inherited together.
Recombination Frequency
The percentage of recombinant offspring, used to measure genetic distance.
Genetic Map Units (cM)
A unit measuring the distance between genes, where 1% recombination equals 1 centimorgan.
Molecular Markers
Sequence variants used to map genes to chromosomal locations.
Chi-square Test
A statistical test used to determine if observed genetic ratios deviate from expected ratios due to chance.
Pedigree Analysis
The study of family inheritance patterns to determine the genetics of a trait.
Autosomal Recessive
A trait that appears in progeny of unaffected parents, often seen in both sexes.
Autosomal Dominant
A rare allele that is dominant, meaning only one copy is needed for the phenotype to appear.
Dimorphisms
Polymorphisms that give rise to alternative common morphs, such as blue vs. brown eyes.
Polygenic Inheritance
Traits controlled by multiple genes rather than a single gene.
Cytoplasmic Segregation
The process where different organelle genotypes segregate as cells divide.
Chiasmata
Physical chromosome conformations that give rise to crossing over during meiosis.
Map Units
A measurement of genetic distance based on recombination frequency.
Double Crossovers
Rare recombination events where two separate crossover events occur within the same chromosome pair.
Reciprocal Cross
A genetic cross where the phenotypes of the male and female parents are switched to test inheritance patterns.
Single Nucleotide Polymorphisms (SNPs)
Genetic variations at a single nucleotide position, used as molecular markers.
Microsatellite Markers
Short tandem repeat sequences used as molecular markers in genetic mapping.
Trihybrid Cross
A cross between individuals heterozygous for three genes, often leading to an 8-class phenotypic ratio.
Segregation Ratios
The expected ratios of offspring phenotypes based on inheritance laws.
Hybrid Vigor
When hybrid offspring show improved traits compared to their purebred parents.
Homozygous
Having two identical alleles for a gene.
Heterozygous
Having two different alleles for a gene.
SRY Gene
A Y-linked gene responsible for male sex determination.
Dominant Mutation
A mutation that produces a phenotype when present in a single copy.
Null Mutation
A mutation that completely inactivates a gene's function.
Centromere
The part of a chromosome that links sister chromatids and is essential during cell division.
Telophase
The final phase of mitosis and meiosis where the nuclear envelope reforms around separated chromosomes.