Lec 10 Flashcards

0
Q

two recombinant chromosomes

A

outer 2 same, middle different

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1
Q
  • calculated by using recombination frequencies
  • meausred in map unites
  • calcualte distnaces along chromosome, using number of base pairs
A

genetic maps

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2
Q

two non recombinant

A

all same

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3
Q

most numerous phenotype

A

nonrecombinant

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4
Q

least numerous

A

double crossover

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5
Q

Lod scores

A

estimates gene distance

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6
Q

genetic markers

A

easy to identifiy

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7
Q

loss of both members of a pair of homologus chromosomes

A

nullisomy

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8
Q

loss of a single chromosome

A

monosomy 2n-1

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9
Q

gain single choromosme

A

trisomy 2n+1

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10
Q

change in number of individual chromosomes

A

anueploidy

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11
Q

tetra

A

2n+2

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12
Q

double trisomy

A

2n+2

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13
Q

double monomy

A

2n-1-1

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14
Q

double terasomy

A

2n+2+2

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15
Q

X inactivation is an example of what?

A

dosage compensaiton

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16
Q

down syndrom

A

trisomy 21

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17
Q

familal down syndrom

A

45 chromosomes part of 21 goes elsewhere example of robertsonian translocation

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18
Q

nail

A

autosomeal dominant trait.. LMX1B

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19
Q

Trisomy 10 Edward Syndrom

A

mental retardation
deaht in year
low set of ears, deformed feet

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20
Q

trisomy 13

A

patau
mr
cleft lip extra fingers big forhead death

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21
Q

trisomy 8

A

normal life

mr

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22
Q

chromosems inherted from same parent

A

uniparental disomy
cystic fibrosis
prader willi

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23
Q

nondisjuction in mitosis region o ftissue is different

A

turners

mosaicism

24
number of sets of chromosmes is different more common in plants
polyploidy
25
extra sets of chromosomes from 2 or MORE species
allopolyploidy
26
extra sets of choromosomes from species
autopolyploidy
27
paracenric
do NOT include chromosome
28
pericentric
DO include chromosome
29
may break gene forme inverstion loop
inversion
30
crossing over of inversion causese
normal non recom 2 non viable one non para
31
a specific set of linked genes non random association btw alles linkage disequilbirum
haplotype
32
method used for postiiioning gnes on chromosomes -mutation will form cell line cancer tumor
somatic cell hybridizaiton
33
Jimison weed
12 trisomimc mutaions each for different pair of choromosmes does nOT effect nuclotie abnormal gene dosage
34
ajacent 1 and 2 segregation
non viable gametes
35
alternate seg
viable gametes
36
seg translocation
large amount of genes are moved
37
translocation
movement of genetic material btw non homologous chromosomes
38
reciprical translocaiton
movement bt nonhomologous chormoosmes | more common than non
39
nonreciprical
momemnt from one to another without exchagne
40
cri du chat snydrom
deletion of shrot arm of chrom 5... child is heterozygous fro deletion results in small head, wide eyes, round face, mR, distinct cry
41
wolf hirschhorn
``` dletion of short arm of 4, small head high forehead wide nose cleft lip and palate sever MR ```
42
Tandem duplication
duplication region is immediatley adjacent
43
displaced duplicaiton
located some displacement from duplicaiton
44
reverse duplication
inversted
45
Inhertiance pattern of bar mutions
unequal cross over, bc they are not well lined up
46
deletion effects
imbalance of gene product, expression of normally recessive gene duplicaiton may cause evolution... could be bad
47
psudodomminat
is recessive but bc of deletion appear domoninat bc both parents do not have gene
48
haplosuficiency
single copy not sufficent to create wild type
49
band rich in A-T base pairs
G band
50
difference in amoounts of CG and AT
Q band
51
centromeric heterochromati
C bnad
52
R band
rich in CG
53
autoploidy
3n
54
of observed double cross over =
coefficentX nubmer of expected
55
coefficent of coincendince
of observed double crossovers/ number of expected double crossoovers
56
inference =
1- coefficent
57
expected number od couclbe crossover
gene one cross overX gene one cross overX total number