Patterns of Inheritance Flashcards

1
Q

Genetic composition.

A

Genotype

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2
Q

Observable characteristics.

A

Phenotype

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3
Q

Variations of a gene.

A

Alleles

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4
Q

Follow a simple pattern of inheritance as defined by Mendel’s laws of dominance. —> Establishes that dominant traits will be expressed over recessive traits.

A

Autosomal Alleles

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5
Q

Lead to expression of the allele whether the individual has 1 or 2 copies of the allele.

A

Autosomal Dominant Alleles

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6
Q

Are only expressed when the individual is homozygous for the allele.
Individuals with 1 copy of the recessive trait are carriers and could pass the recessive allele on to future generations.

A

Autosomal Recessive Alleles

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7
Q

A characteristic pattern of inheritance exhibited by genes located on a sex chromosome (X or Y).

A

Sex-Linked Alleles

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8
Q

Can give rise to a variety of phenotypes because of gene interactions and interactions between genes and their environment.

A

Complex/Multifactoral Traits

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9
Q

Organized profile of an organism’s chromosomes.
A way to characterize the chromosomes located in the nucleus of a eukaryotic cell. —> By number, relative size, shape, and appearance of chromosomes.

A

Karyotype

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10
Q

The identical copies of each chromosome that the centromere joins.

A

Sister Chromatids

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11
Q

The location where the sister chromatids are closest together.

A

Centromeres

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12
Q

An image of chromosomes arranged by size (and other characteristics).
Image of chromosomes from a cell.

A

Karyogram

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13
Q

An organism with the appropriate number of chromosomes for the species.

A

Euploid

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14
Q

An organism with more or less than the appropriate number of chromosomes for the species.

A

Aneuploid

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15
Q

To prevent significant impacts of having an “extra” chromosome, one of the X chromosomes is inactivated (in females).

A

X-Inactivation

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16
Q

Inactive X-chromosome.

A

Barr Bodies

17
Q

Family tree.

18
Q

The 1st identified individual who exhibits an inherited disease or disorder.

A

Propositus

19
Q

If 1 or both alleles are mutated, the individual will exhibit the disorder.
Heterozygous individual with the disorder have a 50% chance of passing on the mutated allele.
Homozygous individual with the mutated allele will pass the mutated allele on to EVERY child.
No carriers for a dominant disorder. —> All individuals with a mutated allele will exhibit the disorder.

A

Autosomal Dominant Disorder

20
Q

Only indictable who exhibit the disorder have 1 or 2 copies of the recessive allele without a dominant allele to mask it.
ex. Sons inherit only 1 X chromosome (from their mothers) so if a mother exhibits this (indicating that both X chromosomes are affected) then 100% of her sons will inherit a mutated X chromosome and exhibit this because they don’t have another X chromosome to mask it.
Family members with only 1 copy of the recessive allele are said to be carriers.

A

Sex-Linked Recessive Disorder

21
Q

A family tree showing which members have the genes for a certain trait.

22
Q

Traits carried on a chromosome other than X or Y.

A

Autosomal Traits

23
Q

Traits that appear on the X or Y chromosome.

A

Sex-Linked Traits

24
Q

Trait that is on the X chromosome.
Shows up more often in males because if they inherit 1 X chromosome that has the trait, they are automatically affected while females are only affected if they inherit an X from each parent that carries the allele for the trait.

A

X-Linked Trait

25
Genetic sequencing method used to determine the genetic sequences of long strands of DNA. DNA is randomly broken up into many small fragments and each fragment is sequenced. Then, a computer program reassembles the DNA fragments. Bioinformatics develop ways to collect, organize, and interpret this data digitally. *Helpful in the diagnosis/management of infectious diseases, cancers, and many biological disorders.*
Shotgun Sequencing
26
The science of collecting and analyzing complex biological data such as genetic codes.
Bioinformatics
27
The rearrangement and exchange of genetic information from different sources. *Essential for organisms because it helps create new genetic types, which form the basis of evolution
Genetic Recombination
28
Choosing to breed organisms that will result in the offspring with desired characteristics. *Hybridization to make offspring that exemplify the best traits of each parent.*
Selective Breeding
29
Selective breeding that occurs when individuals with similar characteristics continue to be bred to keep a caretaking set of traits. —> This makes inbred organisms genetically similar and there’s a high probability that members of the population will receive mutated alleles that lead to disorders.
Inbreeding
30
Have both their original DNA and the genes of other organisms.
Transgenic Organisms
31
Scientists can use a single cell to produce new cells, tissues, or even full organisms. *The nucleus of an egg cell is removed and fused with a donor nucleus, and the resulting embryo can be implanted in the uterus of a surrogate mother.*
Cloning