Genetics Flashcards

(47 cards)

1
Q

The study of genes, which are the units of inheritance

A

Genetics

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2
Q

The carrier of genetic information; single, double-stranded DNA molecule

A

Chromosomes

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3
Q

Two molecules of double-stranded DNA joined in the center by a centromere

A

Chromatid

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4
Q

An ordinary chromosome; one that does not determine sex of the individual

A

Autosome

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5
Q

A chromosome that is causally associated with the sex of an individual

A

Sex chromosomes

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6
Q

Chromosomes of the same kind

A

Homologous chromosomes

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7
Q

The position of a gene on its chromosome; the position of a gene on the genetic map

A

Locus

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8
Q

The region or regions of a chromosome with which the spindle fibers become associated during mitosis and meiosis

A

Centromere

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9
Q

DNA sequences at the tips of chromosomes that protect the tips of chromosomes from erosion and from sticking to each other

A

Telomere

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10
Q

The number of chromosomes in gamates

A

Gametic number

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11
Q

The number of chromosomes in ordinary body cells of an organism

A

Somatic number

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12
Q

The copying of a specific sequence of DNA to produce the corresponding sequence of RNA (mRNA)

A

Transcription

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13
Q

The assembly of a new protein molecule using its amino acid building blocks, as specified by mRNA

A

Translation

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14
Q

Sequence of events in which a body cell duplicates its contents and divides in two

A

Cell cycle

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15
Q

Somatic cells contain two sets of chromosomes are called

A

diploid cells

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16
Q

Phase of cell division that the cell is not dividing

  • replicate its DNA
  • consists of three phases, G1, S, and G2
A

Interphase

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17
Q

consists of nuclear division (mitosis) and cytoplasmic division (cytokinesis) to form two identical cells

A

Mitotic phase

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18
Q

Nuclear division

A

Mitosis

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19
Q

The chromatin fibers change into chromosomes

20
Q

Microtubules align the centromeres of the chromatid pairs at the metaphase plate

21
Q

The chromatid pairs split at the centromere and move to opposite poles of the cell

22
Q

Two identical nuclei are formed around the identical sets of chromosomes now in their chromatic form

23
Q

Cytoplasmic division

24
Q

Reproductive cell division

25
Look alike, paired. chromosomes
Homologous chromosomes
26
Homologous chromosomes pair
Tetrads
27
During Meiosis prophase 1, chromatids of homologous chromosomes form chiasmata wherein matching regions break and then reconnect to the other chromosome
Crossing over
28
Reductive division
Meiosis 1
29
Two haploid cells with replicated sister chromatids go to form four haploid cells with single, unreplicated molecules of DNAs
Meiosis 2
30
One chromosomes in each pair came from the mother, and the other from the father
Homologous chromosomes
31
Each pair of homologous chromosomes
Homologous pair
32
Human karyotype composed of
22 pairs of autosomes | 1 pair of sex chromosomes
33
Alternative forms of gene that code for the same trait and are at the same location on homologous chromosomes are called
alleles
34
Same alleles
Homozygous
35
Different alleles
Heterozygous
36
Genetic makeup of individual
Genotype
37
Physical or outward appearance
Phenotype
38
An allele that dominates or masks the presence of another allele and is fully expressed
Dominant allele
39
An allele whose presence is completely masked
Recessive allele
40
Agglutination occurs when the red cell antigens correspond to the antibodies in the antisera
Forward typing
41
Most common cause of dwarfism
Achondroplasia
42
The probability of combining different alleles
Punnett square
43
When an individual is born with chromosomes added or missing
Aneuploidy
44
Missing 1 chromosome
Monosomy
45
Have an additional chromosomes
Trisomy
46
The most common cause of hemolytic disease of the new born with the major antigen Rh or D
Erythroblastosis fetalis
47
The failure of chromosome pairs to separate properly during cell division
Nondisjunction