Mendelian Genetics Flashcards

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1
Q

what are alleles

A
  • each variation of a gene, which encodes for a slightly different protein
  • are in pairs and represented by 2 letters
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2
Q

what is a phenotype

A

the physical appearance due to a specific gene

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3
Q

what is a genotype

A

genes(alleles) possessed by indivudals

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4
Q

what is homozygous

A

an individual who has 2 identical alleles of a gene

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5
Q

what is heterozygous

A

an individual who has 2 different alleles of a gene

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6
Q

what is a dominant allele

A

A ‘strong’ allele which dominates over the other, causing that phenotype to emerge

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7
Q

what is a recessive allele

A

A ‘weak’ allele which is dominated by the dominant allele, thus its phenotype not being present

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8
Q

what are co-dominant alleles

A

alleles which are equally strong, thus creating mixtures of the phenotype of each allele in an individual

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9
Q

what is a locus

A

the physical position of a gene on a chromosome

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10
Q

what is a carrier

A

an individual who has a recessive allele that does not affect their phenotype, yet still has that allele present

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11
Q

what is a punnet grid +use

A
  • it is a diagram that shows all the possible combinations of alleles for a particular trait
  • used to predict the outcome of genetic crosses (inheritance)
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12
Q

who was Mendel

A
  • austrian priest who investigated inheritance
  • used pea plants to experiment
  • not first person to do this work, first person to count and quantify genetic crosses
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13
Q

what are mono-hyrbrid crosses

A

crossing pure bred individuals with a different allele for a specific trait

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14
Q

what is a di-hybrid cross

A

a cross between two individuals that differ with two traits

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15
Q

What is Mendel’s third law (law of independent assortment)

A
  • genes do not influence each other with regard to sorting alleles into gametes
  • Genes which are located on different chromosomes segregate independently from one another during gamete formation

-ALLELES OF GENES ON NON-HOMOLOGOUS CHROMOSOMES ASSORT INDEPDENTLY DURING MEIOSIS

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16
Q

what are linked genes

A

genes that are located very close to one another on the same chromosome

-don’t follow Mendel’s second law, crossing over less likely to occur

17
Q

what is Mendel’s first law (law of dominance)

A

In a cross of parents that are pure for contrasting traits, only one form of the trait will appear in the next generation. Offspring that are hybrid for a trait will have only the dominant trait in the phenotype.

18
Q

what is Mendel’s second law (law of segregation)

A

During the formation of gametes (eggs or sperm), the two alleles responsible for a trait separate from each other. Alleles for a trait are then “recombined” at fertilization, producing the genotype for the traits of the offspring.

19
Q

what is an example of co-dominance + both multiple alleles

A

blood type

20
Q

what are autosomal sex chromosomes

A

22 pairs of autosomes, 1 pair of sex chromosomes
-sex chromosomes control male (XY) and female (XX)
-

21
Q

what determines the sex of the offspring, the genetic makeup of the sperm or the genetic makeup of the egg

A

the genetic makeup of the sperm (X or Y) determine the gender

22
Q

what is sex-linkage

A
  • genes carried by sex chromosomes

- sex-linkage is the assosiation of a trait with gender (gene controls traits on a sex chromosome)

23
Q

where do males and females recieve x-linked genes from

A
  • male from mom (1copy): one allele for a particular trait

- female from both parents (2 copies)

24
Q

what are the symbols for sex-linked genes

A
  • XA=normal allele

- Xa= recessive allele

25
Q

what are heterozygous females with X-linked disorders called

A

carriers

26
Q

what are examples of sex-linkage disorders

A
  • hemophilia

- color blindness

27
Q

what is hemophilia

A
  • sex linked
  • woman is carrier
  • recessive
  • 50% of sons inherit disease, 50% of daughters carriers
  • daughters of sons will be carriers, sons unaffected (only girls receive X-chromosome)
28
Q

what is color blindness

A

-inability to see certain colors
-common: inability to see red and green
-x-linked disorder
-ressive
-males usually have it
-

29
Q

what are autosomal disorders

A
  • disorders which affect males and females equally
  • dominant and recessive types
  • takes only 1 copy of gene to cause disorder
  • if child inherits diesease, at least one parent has it
30
Q

example of autosomal disorder

A

-cystic fibrosis

31
Q

what is a pedigree

A

-a chart of genetic history of family over generations

32
Q

why is a pedigree chart used

A
  • to deduce is trait is dominant or recessive, inherited, sexlinked or autosomal
  • to deduce the genotype of indivudals
  • to deduce the probability of a child having a condition
33
Q

tips to read a pedigree chart

A
  • if most males have it, its X-linked
  • if its a 50/50 ratio of male and women; autosomal
  • if the disorder is autosomal dominant, one of the parents must have disorder
  • if autosomal recessive, none of the parents has to have the disorder to be heterozygous