Non-Mendelian Genetics: Non-Mendelian Genetics and Heredity Flashcards

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1
Q

Codominance

A

two dominant alleles are expressed at the same time

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2
Q

Incomplete Dominance

A

no allele is completely dominant. BLENDING of phenotypes occurs to make a 3rd phenotype.

–> Only assume heterozygous genotype represents blending if told so. Otherwise, always assume the heterozygous genotype shows for the same dominant phenotype as homozygous dominant.

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3
Q

Sex-linked Traits

A

traits found on a sex chromosome (X or Y), usually refers to X traits (because only males have Y)

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4
Q

Sex-linked Traits

Relationships between Parents and Children

A
  • Fathers cannot pass sex-linked traits to their sons because males receive their X-chromosome from their mothers.
  • Mothers can pass sex-linked alleles to both sons and daughters.
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5
Q

Sex-Linked Traits

Relationships between X and Y Chromosomes

A
  • Most X-linked genes have no homologous loci on the Y chromosome.
  • Most genes on the Y chromosome not only have no X counterparts, but they encode traits found only in males
  • The X chromosome is larger than the Y chromosome, therefore there are more traits present on the X chromosome.
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6
Q

Pedigrees

A

tracks a specific trait within family history, squares represent males, circles represent females, unshaded (white) are unaffected, and shaded (black) are affected.

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7
Q

Autosomal Recessive Pedigrees

A

recognized because the trait skips a generation but is still equally shown in both genders.

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8
Q

Sex-linked Recessive Pedigrees

A

recognized by the trait skipping a generation and recognition that the trait is much more common in males. Specifically with this pattern, any affected female must have an affected father.

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9
Q

Pedigrees

Complicated Information about Pedigrees

A
  • If the trait is identified as autosomal dominant, all unaffected individuals must be homozygous recessive
  • All affected individuals must have at least one dominant allele
  • People who marry into the families can either be identified as homozygous recessive or known with only one dominant trait (the other trait is unknown).
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10
Q

Carriers

A

FEMALES who has inherited a recessive allele of a gene that is linked to a genetic condition. However, she doesn’t show traits or symptoms of the condition because her second allele for that gene is normal.

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