Genne Flashcards

(38 cards)

1
Q

Chromosone Theory of Heredity

A

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2
Q

Sex chromosomes

A

a chromosome which determines the sex, of two kinds

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3
Q

autosome

A

any chromosome that is not a sex chromosne

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4
Q

X chromosone

A

a sex chromosone

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5
Q

Y Chromosone

A

a sex chromosne

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6
Q

Mutation

A

permanent change to a genetic sequence

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7
Q

Chromosonal mutation

A

A chromosome mutation causes changes in the structure or number of chromosomes in a cell

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8
Q

nondisjunction

A

abnormal distribution of chromosomes in the daughter nuclei due to failed splitting of homologous paird

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9
Q

point mutation

A

a mutation affecting a very small amount of nucleotiudes in a gene sequence

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10
Q

substitution

A

type of point mutation where a nucelotide is replaced with a different one resulting in an altered sequence during trranslation

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11
Q

insertion

A

Insertion of one or more nuceletides in a gene sequence

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12
Q

deletion

A

where part of a chromosome or gene sequence is deleted missing

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13
Q

frameshift mutation

A

genetic mutation where by insertion of deletion a sequence is changed the way its read

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14
Q

incomplete dominance

A

where one allele does not completely dominate the other and results in a new phenotype

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15
Q

codominance

A

on a heterozyugote resulting in offspring that’s phenotype is neither dominant nor recessive

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16
Q

polygenic inheritance

A

a single trait that is influenced by two or more allele (hair color)

17
Q

multiple allele inheritance

18
Q

translocation

A

chromosomal segment is moved from one position to another

19
Q

duplication

A

duplication of a region of DNA that contains a gene.

20
Q

Downsyndrome

A

An extra copy of chromosome 21

21
Q

Klinefelters Syndrome

A

Boy is born with an extra x chromosne

22
Q

Turners Syndrome

A

Where women only have one x chromosne

23
Q

Amniocentesis

A

screen for developmental abnormalities in a fetus.

24
Q

karyotype

A

The number and visual appearance of the chromosomes oiin the cell

25
hemophilia
Where blood cannot clot well (inherited)
26
sicklecell anemia
inherited abnormal hemoglobin
27
Duchenne Muscular Dystrophy
mutattion if the DMD gene that is inherited. encodes the muscle protein, dystrophin
28
cystic fibrosis
heredity dfisorder which production of abnormally thick mucus, leading to the blockage of the pancreatic ducts, intestines, and bronchi and often resulting in respiratory infection
29
Tay-Sachs Disease
an inherited metabolic disorder in which certain lipids accumulate in the brain, causing spasticity and death in childhood.
30
polydactyly
a condition in which a person or animal has more than five fingers or toes on one, or on each, hand or foot. Iherited
31
mutagen
a chemical substance which causes genetic mutation
32
inbreeding
bred from closely related people over decades
33
hybridization
mating organisms of different varieties or species to create a hybrid
34
Huntington's disease
a hereditary disease marked by degeneration of the brain cells and causing chorea and progressive dementia.
35
monosomy
having only one chromosone
36
trisomy
having an extra chromosone
37
somatic mutation
Alterations in DNA that occur after conception
38
germ mutation
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