Genetics Questions

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17 Terms

1
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where are chromosomes found in a cell?

in the nucleus.

2
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what are homologous chromosomes?

pairs of chromosomes similar in size, location & banding pattern.

3
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how many chromosomes do humans have?

46 chromosomes (23 pairs).

4
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what are sex chromosomes in females and males?

females: XX

males: XY

5
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what is a karyotype?

a picture of all chromosomes arranged from largest to smallest in pairs.

6
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what can a karyotype show besides chromosome number?

the sex of an individual and chromosomal abnormalities.

7
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what are the parts of a DNA nucleotide?

deoxyribose sugar, phosphate group & nitrogen base.

8
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Which Nitrogen bases pair together?

A (adenine) pairs with T (thymine)

C (cytosine) pairs with G (guanine )

9
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what does a codon code for?

a specific amino acid.

10
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what is the function of mitosis?

to produce two genetically identical diploid daughter cells for growth and repair.

11
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what is the outcome of meiosis?

four genetically different haploid gametes.

12
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define mutation.

a change in the DNA sequence.

13
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name two types of mutations.

point mutation & frame shift mutations.

14
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what is a chromosomal mutation?

a change in chromosome structure, affecting many genes.

15
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what are 5 examples of chromosome mutations?

duplication, deletion, inversion, insertion & translocation.

16
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what is the difference between dominant and recessive traits?

dominant traits require 1 allele to show.

recessive traits require 2 alleles to show.

17
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what is co-dominance?

both alleles are fully expressed (eg. AB blood type).