Unit 8 - Genetics Flashcards

1
Q

nondisjunction

A

when chromosomes don’t separate properly during meiosis, too many or too few in each cell

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2
Q

trisomy

A

having an extra chromosome in zygote cell (3 instead of 2)

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3
Q

organisms with extra chromosomes usually ____, organisms missing chromosomes usually _____

A

survive, die

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4
Q

polyploidy

A

too many chromosomes

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5
Q

what does polyploidy cause in animal cells

A

death

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6
Q

what does polyploidy cause in plants

A

doesn’t do anything, common in plants

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7
Q

deletion

A

large section removed

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8
Q

duplication

A

section is duplicated

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9
Q

inversion

A

sections flip order

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10
Q

reciprocal translocation

A

part of one chromosome exchanged with another

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11
Q

ABCD – ACD

A

deletion

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12
Q

ABCD – ABCBCD

A

duplication

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13
Q

ABCD – ACBD

A

inversion

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14
Q

ABCD – MNOD
MNOP–ABCP

A

reciprocal translocation

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15
Q

genetics

A

study of how traits are passed from one gen to the next, specifically how genes affect that

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16
Q

heredity

A

passing of characteristics from parent to offspring

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17
Q

gene

A

section of DNA found on chromosome

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18
Q

traits

A

characteristic of an individual

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19
Q

Gregor mendel

A

Austrian monk that studied pea plants to determine how traits are passed, “father of modern genetics”

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20
Q

principle of dominance

A

dominant and recessive traits

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21
Q

segregation

A

traits for tallness and shortness seperated during formation of gametes

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22
Q

homo dominant:hetero:homo recessive

A

genotypic ratio

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23
Q

dominant:recessive

A

phenotypic ratio

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24
Q

shows two types of gametes from each parent in punnet square w/ 4 boxes, one trait

A

monohybrid cross

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25
punnet square that shows two traits in 16 boxes
dihybrid cross
26
mendelian inheritance
dominant or reessive, homo and hetero
27
one allele not completely dominant over another, phenotype is between homo phenotypes
incomplete dominance
28
red and white flower crossed, pink result
incomplete dominance
29
heterozygote shows phenotypes of both alleles
codominance
30
white and black chicken crossed, offspring has black and white feathers
codominance
31
gene with more than two alleles
multiple alleles
32
eye color, each person has two alleles in a diploid cell for eye color, many eye color alleles in the human population
multiple alleles
33
blood genotype AA or AO, phenotype?
A
34
blood genotype BB or BO, phenotype?
B
35
blood genotype AB, phenotype?
AB
36
blood genotype OO, phenotype?
O
37
traits controlled by two or more genes
polygenic traits
38
skin color controlled by more than four genes
polygenic trait
39
ability of a gene to affect an organism in multiple ways (many phenotypes)
pleitropy
40
sickle-cell disease, causes many symptoms
pleitropy
41
gene at one location alters expression of a gene in another location
epistasis
42
BB/Bb/bb determines coat color but CC/Cc/cc determines pigment
epistasis
43
chromosome pairs 1-22
autosomes
44
chromosomes that determine sex
sex chromosomes, pair 23
45
XX (male or female)
female
46
XY (male or female)
male
47
gene is only found on X chromosome
sex-linked traits
48
male pattern baldness, colorblindness, hemophilia
sex-linked traits
49
someone who carries a sex-linked trait but is not affected by it
carrier, usually women
50
women can only have a sex-linked disease if...
father has it and mother is carrier or has it
51
what is trisomy 21?
down syndrome
52
most genetic disorders are in (recessive/dominant) alleles
recessive
53
condition that causes formation of thick mucus in lungs and digestive tract
cystic fibrosis
54
about how many white Americans carry cystic fibrosis
1 in 20
55
condition that causes fat to accumulate in central nervous system
tay-sachs disease
56
who normally has tay-sachs disease
Jews from eastern europe
57
is cystic fibrosis caused by recessive or dominant alleles
recessive
58
is tay-sachs disease caused by recessive or dominant alleles
recessive
59
is tay-sachs disease lethal
yes
60
condition where the body can't digest the amino acid phenylalanine to amino acid tyrosine
phenylketonuria (PKU)
61
what does phenylketonuria cause
damage to the central nervous system, sometimes retardation in infants if not found
62
condition that causes breakdown of parts of the brain
huntington's disease
63
when does onset huntington's disease happen
30-50 yrs of age
64
diagram of how traits are inherited
pedigree
65
heterozygous person who "carries" a recessive trait and may pass it onto their children but it doesn't affect them
carrier