Genetics and Key Science Skills Flashcards

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1
Q

Genome

A

All of the genetic material in an individual or cell

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2
Q

Allele

A

A variation of a gene at a particular gene locus

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3
Q

Gene

A

The hereditary unit, which is a section of DNA occupying a specific location on a chromosome. It determines a characteristic of an organism by directing the formation of a protein.

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4
Q

Genotype

A

The allele combination of an individual

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5
Q

Phenotype

A

The physical, behavioural or physiological characteristics of an organism which are a result of the combination of the genotype and environment.

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6
Q

Homozygous

A

Having identical alleles at the same gene locus on homologous chromosomes. Sometimes referred to as ‘purebred’.

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7
Q

Heterozygous

A

Having different alleles at the same gene locus on homologous chromosomes. Sometimes referred to as ‘hybrid’.

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8
Q

Carrier

A

An individual that has inherited a copy of a recessive allele for a particular trait, but does not display the trait due to the presence of a dominant allele.

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9
Q

Dominant (allele)

A

An allele that is expressed in the heterozygous genotype

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10
Q

Recessive (allele)

A

An allele that is only expressed when the genotype is homozygous for that allele

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11
Q

Punnett Square

A

A table that shows the possible genotypes of offspring given the genotypes of the two parents

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12
Q

F1 generation

A

The offspring of the parent generation

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13
Q

F2 generation

A

The offspring of the F1 generation

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14
Q

Monohybrid Cross

A

Determination of the possible genotypes and phenotypes of offspring at a particular gene locus

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15
Q

Dihybrid Cross

A

Determination of the possible genotypes and phenotypes of offspring at two gene loci

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16
Q

Co-dominance

A

Two alleles from the genotype are both fully expressed in the phenotype of a heterozygote

17
Q

Polygenic

A

The observed phenotype is the result of contributions from two or more genes, and does not follow Mendelian genetics

18
Q

Multifactorial

A

The observed phenotype is the result of contributions from one or more genes plus environmental factors.

19
Q

Sex-linked trait

A

A trait that occurs as a result of a gene on a sex chromosome. This may be on the X-chromosome (X-linked) or the Y-chromosome (Y-linked)

20
Q

Test cross

A

A cross performed between an individual showing a dominant phenotype with a homozygous recessive individual, to determine the genotype of the individual with the dominant phenotype

21
Q

Pedigree

A

A chart showing the relationship between family members and whether they show an inherited trait

22
Q

Gene linkage

A

When two genes are located on the same chromosome. This will result in ‘parental’ combinations of alleles which are inherited more often than ‘recombinant’ combinations

23
Q

Phenotype ratio of a monohybrid cross when both parents are heterozygous

A

3:1

24
Q

Phenotype ratio of a monohybrid test cross if the individual with the dominant trait is heterozygous

A

1:1

25
Q

Phenotype ratio of a dihybrid cross where both parents are double heterozygotes

A

9:3:3:1

26
Q

Phenotype ratio of a dihybrid test cross if the parent with dominant phenotypes is a double heterozygote (no gene linkage)

A

1:1:1:1

27
Q

Phenotype ratio of a dihybrid test cross where the parent with dominant phenotypes is a double heterozygote and there is gene linkage (assume crossing over occurs)

A

many:many:few:few

28
Q

Evidence for a recessive inheritance pattern

A

An affected individual has two unaffected parents, for example….

29
Q

Evidence that shows a dominant inheritance pattern is likely (but not definitive)

A

All affected individuals have an affected parent

30
Q

Evidence that shows a recessive trait is X-linked

A

An affected mother passes the trait onto all sons

31
Q

Evidence that a dominant trait is X-linked

A

An affected father passes the trait onto all daughters

32
Q

Evidence that a recessive trait is autosomal

A

An affected mother has an unaffected son

33
Q

Evidence that a dominant trait is autosomal

A

An affected father has an unaffected daughter