Looks like no one added any tags here yet for you.
Phenotype
Observable Characteristic
Alleles
Alternate forms of a gene
Independent Assortment
alleles of one gene separate into gametes randomly with respect to alleles of other genes
Gamete
Reproductive cells containing only one copy of each gene
Gene
The heritable entity that determines a trait
Segregation
The separation of the two alleles of a gene into different gametes
Heterozygote
An individual with two different alleles of a gene
Dominant
The allele expressed in the phenotype of the heterozygote
F1
Offspring of the P generation
Testcross
The cross an individual of ambiguous genotype with a homozygous recessive individual
Genotype
The alleles an individual has
Recessive
The allele that does not contribute to the phenotype of the heterozygote
Dihybrid Cross
A cross between individuals both heterozygous for two genes
Homozygote
Having two identical alleles of a given gene
Epistasis
The alleles of one gene mask the effects of alleles of another gene
Modifier Genes
Genes who alleles alter phenotypes produced by the action of other genes
Conditional lethal
A genotype that is lethal in some situations but viable in others (eg. high temp)
Permissive conditon
Environmental condition that allows conditional lethals to live
Reduced penetrance
Less than 100% of the individuals possessing a particular genotype express it in their phenotype
Complex trait
A trait produced by the interaction of alleles of multiple genes and often also the environment
Incomplete dominance
The heterozygote resembles neither homozygote
Codominance
Both parental phenotypes are expressed in the F1 hybrids
Mutation
A heritable change in a gene
Pleiotropy
One gene affects more than one trait
Variable expressivity
Individuals with the same genotype have related phenotypes that vary in intensity
Meiosis
One diploid cell gives rise to four haploid cells
Gametes
Haploid germ cells that unite at fertilization
Karyotype
The array of chromosomes in a given cell
Mitosis
One diploid cell gives rise to two diploid cells
Interphase
The part of the cell cycle during which the chromosomes are not visible
Synapsis
Pairing of homologous chromosomes
Sex Chromsomes
X and Y
Cytokinesis
Division of the cytoplasm
Anaphase
The time during mitosis when sister chromatids seperate
Chromatid
One of the two identical halves of a replicated chromosome
Autosomes
Chromosomes that do not differ between the sexes
Centromeres
The sites of the closest connections between sister chromatids
Centrosomes
Microtubule organizing centers at the spindle points
SRY
Y-linked gene that determines maleness
Dosage compensation
Processes that equalize the dosage of X-linked gene products in the somatic cells of males and females
Sex-linked
The inheritance pattern of genes on X chromosome
Hemizygous
Describe genes present in only one copy such as those on the X in males
Pseudoautosomal regions (PAR1/2)
The tips of X and Y chromosomes
Nondisjunction
Failure of homolog separation in meiosis I or chromatid separation in meiosis II
X-Chromosome inactivation
In XX cells, most genes a random X chromosome are turned off
Klinefelter syndrome
XXY Males
Turner syndrome
XO females
Oogonia
Cells in the ovary that undergo mitosis
Oocytes
Cells in the ovary that undergo meiosis
Spermatid
Haploid cell at the end of meiosis II that will become a sperm
Spermatocytes
Cells in the testes that undergo meiosis to create spermatid
Epistatic
gene that is masking other gene
Hypostatic
gene that is being masked
Additive
Four distinct F2 phenotypes, 9:3:3:1
Recessive Epistasis
Homozygous recessive allele of one gene masks both alleles, 9:3:4
Reciprocal recessive epistasis
When homozygous recessive of either gene masks the dominant allele of the other gene, 9:7
Dominant Epistasis 1
Dominant allele of one gene hides effects of both alleles of the other gene, 12:3:1
Redundancy
Only one Dominant allele of either two genes is necessary to produce phenotype, 15:1
Complementation
Mutations in two different genes. For example aaBB x AAbb, both have no hearing, the child will have hearing because it is heterozygous
Noncomplementation
Mutations in the same gene. For example AAbb x AAbb, both have no hearing, the child will not have hearing.
Penetrance
How many members of a population with a particular genotype, show the expected phenotype
Complete Penetrance
Mendels Studies
Incomplete Penetrance
75% percent of the people with mutant allele get the disease
Expressivity
The degree or intensity a genotype is expressed in phenotype
Modifier Genes
Alter the phenotype produced by alleles of other genes
Permissive
Range of temps that allele is functional
Restrictive
Range of temps that allele is not functional
Conditional lethal
allele is lethal under certain conditions
Discontinuous Trait
Two distinct phenotypes, smooth/wrinkled
Continuous Trait
Trait that has a variation of phenotypes, height/weight
G1
Growing and preparation for S phase
S phase
DNA synthesis and chromosome duplication
G2
Growth and preparation for mitosis
Reductional vs Equational Division
reductional division reduces the number of chromosomes in a cell, while equational division does not
Autosome
Chromosome not involved in sex determination
Sex Chromosome
Chromosome that determine sex of an organism