Mono hybrid inheritance Flashcards

1
Q

Define Inheritance

A

the passing on of genetic information from one generation to the next.

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2
Q

Define trait

A

a distingushing quality or characteristic

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3
Q

Define Gene

A

genetic information which is transferred from a parent to offspring in the chromosomes

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4
Q

Define allele

A

Is one of the possible form of a gene

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5
Q

define heterozygous

A

When an organism has two different alleles for a certain characteristic

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6
Q

Define homozygous

A

When an organism has two identical alleles

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7
Q

Define dominant

A

Traits that are always expressed (visible in the organism )

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8
Q

Define reccesive

A

Traits that are only seen when they are the only ones present ( the trait is marked )

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9
Q

Define phenotype

A

the set of observable characteristics of an individual

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10
Q

Define Genotype

A

the genetic make up of an organism

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11
Q

Define punnet square

A

A diagram that is used to predict an outcome of a particular cross

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12
Q

Define Monhybrid

A

The offspring of individuals that differ with respect to a particular gene

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13
Q

Define Co Dominance

A

The dominant gene does not completely suppress the reccessive gene, allowing both genes to be diaplayed at the same time without any blending

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14
Q

Define incomplete dominance

A

When a cross between an organism with two different phenotypes produce offspring with a third phenotype that is a blending of the parent

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15
Q

Define sex linked disease

A

Are genetic disorders that through one of the sex chromosomes X or Y

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16
Q

Define Haemophilia

A

A genetic disorder where blood clotting is impaired, leading to prolonged bleeding. The gene for hemophilia is located on the X chromosome, so it primarily affects males who inherit the affected X chromosome from their carrier mothers.

17
Q

Complete dominance

A

When the dominant allele completely covers up the recessive allele

18
Q

who are more likely to carry sex linked diseases

A

Since males have only one X chromosome (XY), they are more likely to manifest sex-linked disorders if they inherit the affected allele.

19
Q

Describe red color blindness

A

red-green color blindness, are caused by mutations in genes located on the X chromosome. This condition is more prevalent in males.

20
Q

Describe fragile X Syndrome

A

The most common inherited cause of intellectual disability, caused by a mutation in the FMR1 gene on the X chromosome. It affects both males and females, but males typically have more severe symptoms.

21
Q

Cleft palate

A

The roof of the mouth (palate) is formed between the sixth and ninth weeks of pregnancy. A cleft palate happens if the tissue that makes up the roof of the mouth does not join together completely during pregnancy.