chapter 9 Flashcards

1
Q

early mistake notion that hereditary info combined like fluids

A

blending inheritance

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2
Q

australian munk who worked with pea plants , cross pollinated,

A

gregor mendell

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3
Q

observable traits of an organism

A

pheotype

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4
Q

actual set of alleles passed by an organism

A

genotype

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5
Q

2 copies of the same allele

A

homozygous

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6
Q

2 different alleles for different versions of the same trait

A

heterozygous

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7
Q

allele that masks the effect of another allele

A

dominant

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8
Q

allele that are masked

A

recessive

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9
Q

presence of at least one dominant allele that determines phenotype

A

simple dominance

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10
Q

cross between individuals that are both heterozygous

A

monohybrid cross

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11
Q

cross between individuals that are both heterozygous

A

dihybrid cross

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12
Q

condition in which both alleles are expressed fully in heterozygous individuals

A

codominance

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13
Q

condition which heterozygous individuals have intermediate phenotype

A

incomplete dominance

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14
Q

interactions between multiple genes determines phenotype also known as polygenic inheritance

A

epistasis

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15
Q

what effects phenotype besides genetic make up?

A

enviroment

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16
Q

colorless outer layer of corn

A

pericarp

17
Q

layer just inside pericarp, may be colored of corn

A

aleurone

18
Q

tissue used as nutrient supply for corn embryo

A

endosperm

19
Q

chart showing relationship and presence of traits

A

pedigree

20
Q

various disorders that are controlled by single gene effects effect how many people?

A

1/200

21
Q

result from a dominant allele on an autosomal (non-sex chromosome)

A

autosomal dominant

22
Q

autosomal dominant: form of dwarfism result of mutant FGFR-3- gene, homozygous dominant individuals die before birth

A

achondroplasia

23
Q

autosomal dominant: absence of an iris, mostly blind,

A

aniridia

24
Q

autosomal dominant: result of mutant gene on chromosome 4, symptoms late in life, neurodegenerative disorder, jerk movement, impaired memory, dementia, anxiety depression

A

huntingtons disease

25
Q

autosomal dominant: mutant gene for connective tissue, individuals are tall and lanky, heart problems, dislocation of retna, osteoarthritis, spinal issues

A

marfan syndrome

26
Q

autosomal dominant: caused by gene coding for protein subunit , results in abnormal nucleus leading to accumulated DNA damage, premature aging, ONLY the result of a mutation not inherited!

A

hutchinson-gillford progeria

27
Q

disorders that are only observed in individuals that have two copies of a recessive allele

A

autosomal recessive

28
Q

autosomal recessive: absence of pigment, skin cancer risk,

A

albinism

29
Q

autosomal recessive: due to mutant recessive allele of CFTR gene, results in accumulation of thick mucus, normal bacterial infections

A

cystic fibrosis

30
Q

autosomal recessive: results in nonfunctional liver enzyme that breaks down phenylalanine to tyosine, toxin to the brain,

A

phenyletonouria (PKU)

31
Q

autosomal recessive: due to recessive allele of HEXA gene, codes for a enzyme that breaks down a particular kind of lysosome, wont break them down, accumulate in nerve cells, results in seizure, blind,def, paralysis, and death by 5

A

tay-sachs disease

32
Q

heterozygous individuals (Aa) have advantage over dominant (AA) , ofter resistant to other diseases

A

heterozygous advantage

33
Q

traits encoded by genes on sex chromosomes, specifically the X chromosome

A

x-linked recessive traits