Term
blending hypothesis (genes) |
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Definition
two traits blend together (yellow + blue = green) |
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Term
particulate hyphothesis (genes) |
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Definition
idea that parents pass down heritable traits |
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Term
why did mendel chose pea plants for his reasearch? (four reasons) |
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Definition
- there are many varieties with distinct heritable features, (characters) and character variants (traits)
- mating of plants can be controlled
- each pea plant has sperm producing organs (stamens) and egg producing organs (carpels)
- Cross pollination can be achieved by dusting one plant with pollen from another
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Term
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Definition
observable heritable feature |
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Term
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Definition
any detectable variant in a genetic character |
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Definition
plants that produce offspring of the same variety when they self pollinate |
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Term
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Definition
the breeding between two contrasting true breeding varieties |
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Term
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Definition
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Term
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Definition
hybrid offspring of P generation |
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Term
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Definition
generation produced when F1 individuals self pollinate |
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Term
what did mendel call what we now call genes? |
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Definition
what mendel called a heritable factor, we now call genes |
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Term
first concept of mendels hypothesis |
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Definition
alternative versions of genes account for vaiations in inherited characters. for example, the gene for flower color exists in two versions, one for purple flower and the other for white flower. |
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Term
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Definition
alternative versions of a gene |
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Term
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Definition
location of a gene. each gene resides at a specific locus on a specific chromosome |
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Term
second concept of mendel's hypothesis |
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Definition
for each character, an organism inherits two alleles, one from each parent |
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Term
third concept of mendel's hypothesis |
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Definition
if the two alleles at a locus differ, then one is dominant and determines the organisms appearance, and the other is recessive and has no noticeable effect on appearance. for example, F1 plants had purple flowers because the alleles for that trait is dominant |
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Term
fourth concept of mendel's hypothesis.
the law of segregation |
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Definition
two alleles for a heritable character seperate during gamete formation and end up in different gametes |
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Term
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Definition
a diagram for predicting the results of a genetic cross between individuals of known genetic makeup |
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Term
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Definition
organism with two identical alleles for a character |
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Term
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Definition
organism has two different alleles for a gene |
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Term
which is true breeding homo or heterozygotes |
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Definition
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Term
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Definition
organisms physical apperance, physical manifestation of a gene |
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Definition
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Term
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Definition
breeding a mystery organism with a homozygous recessive organism. if any offspring display the recessive phenotype, the mystery parent must be heterozygous |
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Term
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Definition
an organism that is heterozygous with respect to a single gene of interest. all the offspring from a cross between parents homozygous for differnt alleles a re monohybrids. for example parents of gneeotype AA and aa produce a monohybrid of genotype Aa. |
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Term
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Definition
a cross between heterozygotes. cross following a single character |
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Term
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Definition
an organism that is heterozygous with respect to two genes of interest. all the offspring from a cross between parents doubly homozygous for different alleles are dihybrids. for example, parents of genotypes AABB and aabb produce a dihybrid of genotype AaBb. |
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Term
law of independent assortment
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Definition
states that each pair of alleles segregates independently of each other pair of allels during gamete formation. genes located near each other on the same chromesome tend to be inherited together |
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Term
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Definition
when phenotypes of the heterozygote and the dominant homozygote are identical |
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Term
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Definition
the phenotype of F1 hybrids is somewhere between teh phenotypes of the parental varieties |
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Term
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Definition
two dominant alleles affect teh phenotype in seperate, distinguishable ways. both show up |
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Term
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Definition
fatal disease that caused by dysfunctional enzyme making the brain accumlate lots of lipids
recessive at organism level, incompletely dominant at biochemical level and codominant at the molecular level |
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Term
dominant alleles are not necessarily more commin in populations than recessive ones. why is that? |
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Definition
natural selection picks out good traits |
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Term
what are teh four phenotypes of blood? |
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Definition
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Term
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Definition
ability for single gene to have multiple effects |
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Term
name two diseases that pleiotropic alleles are responsible for |
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Definition
cystic fibrosis, sickle cell |
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Term
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Definition
when a gene at one locus alters teh phenotypic expression of a gene at a second locus |
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Term
name an example of epistasis |
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Definition
a mouse has a gene that determines pigment color, B for black and b for brown. another gene determines whether the pigment is deposisted into the hair, C, for color and c for no color |
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Term
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Definition
heritbale feature that varies continuously over a range rather than in an either or fasion |
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Term
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Definition
an additve ffect of two or more genes on a single phenotypic character. |
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Definition
phenotypic range of a genotype influenced by the environment. for example gydrangea flower of the same genotype range from blue-violet to pink depending on soil acidity. |
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Term
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Definition
reffering to phenotypic character tha is influenced by multiple genes and environmental factors |
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Term
why aren't humans good subjects for genetic research? |
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Definition
- generation time is too long
- parents produce relatively few offspring
- breeding experiements are unacceptable
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Term
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Definition
family tree that describes the interrleationships of parents and children across generations |
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Term
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Definition
heterozygous individuals who carry recessive allele but are phenotypically normal |
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Term
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Definition
mating between close relatives, which increases chance of mating between two carriers of the same rare allele that can cause diseases |
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Term
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Definition
common lethel disease resulting in defective or abesnt chloride transport channels in plasma membranes. mucus build up in internal organs |
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Term
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Definition
disease caused by substitution of an amino acid in the hemoglobin protein in red blood cells |
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Term
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Definition
dwarfism caused by rare domint allele |
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Term
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Definition
degenerative disease of the nervous system |
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Term
what do genetic counselors do? |
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Definition
provide information to prospective parents concerned about a family history for a specific disease |
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Term
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Definition
when the liquid that bathes teh fetus is removed and tested |
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Term
chorionic villus sampling |
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Definition
CVS is when a sample fo the placenta is removed and tested. |
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Term
two other examples of fetal testing |
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Definition
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Term
what's the difference between dominant and recessive? |
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Definition
dominant shows up in the phenotype and recessive is usually not seen |
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Term
what's the difference between heterozygous and homozygous |
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Definition
heterozygous contains two different alleles for a trait and homozygous contains two of the same allele for a trait |
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Term
what's the difference between a genotype and a phenotype? |
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Definition
genotypes are unseen parts of the genetic makeup and phenotypes are the seen results of the genotype |
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Term
what's are teh differences among complete dominance, incomplete dominance, and codominance |
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Definition
complete has only one phenotype show up, incomplete has an interemediate between two phenotypes show up and codominance shows multiple phenotypes showing up |
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Term
explain how carrier recognition, fetal testing and newborn screening can be used in genetic screening and counseling |
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Definition
parents will be able to see if there are any gene related problems with the child |
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