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KEY CONCEPT The chromosomes on which genes are located can affect the expression of traits.
Two copies of each autosomal gene affect phenotype. Mendel studied autosomal gene traits, like hair texture.
(dominant) Mendel’s rules of inheritance apply to autosomal genetic disorders. ,[object Object]
Disorders caused by dominant alleles are uncommon.,[object Object]
[object Object]
All of a male’s sex-linked genes are expressed.
Males have no second copies of sex-linked genes.,[object Object]
Expression of sex-linked genes is similar to autosomal genes in females.
X chromosome inactivation randomly “turns off” one X chromosome. ,[object Object]
Phenotype can depend on interactions of alleles. In incomplete dominance, neither allele is completely dominant nor completely recessive. Heterozygous phenotype is intermediate between the two homozygous phenotypes Homozygous parental phenotypes not seen in F1 offspring
Codominant alleles will both be completely expressed. ,[object Object]
The ABO blood types result from codominant alleles.
Many genes have more than two alleles.,[object Object]
[object Object],[object Object]
 The sex of sea turtles   depends on both genes   and the environment
 Height is an example of a   phenotype strongly affected   by the environment.,[object Object]
Mutant Wild type Gene linkage was explained through fruit flies.  Morgan found that linked traits are on the same chromosome. Chromosomes, not genes, assort independently during meiosis.
Linked genes are not inherited together every time. ,[object Object],[object Object]
[object Object]
gene A and gene B cross over 6.0 percent of the time
gene B and gene C cross over 12.5 percent of the time
gene A and gene C cross over 18.5 percent of the time,[object Object]
Human genetics follows the patterns seen in other organisms.  The basic principles of genetics are the same in all sexually reproducing organisms. Inheritance of many humantraits is complex. Single-gene traits areimportant in understandinghuman genetics.
Y X Females can carry sex-linked genetic disorders.  Males (XY) express all of their sex linked genes. Expression of the disorder depends on which parent carries the allele and the sex of the child.

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Unit 7 Chromosomes And Phenotype

  • 1. KEY CONCEPT The chromosomes on which genes are located can affect the expression of traits.
  • 2. Two copies of each autosomal gene affect phenotype. Mendel studied autosomal gene traits, like hair texture.
  • 3.
  • 4.
  • 5.
  • 6. All of a male’s sex-linked genes are expressed.
  • 7.
  • 8. Expression of sex-linked genes is similar to autosomal genes in females.
  • 9.
  • 10. Phenotype can depend on interactions of alleles. In incomplete dominance, neither allele is completely dominant nor completely recessive. Heterozygous phenotype is intermediate between the two homozygous phenotypes Homozygous parental phenotypes not seen in F1 offspring
  • 11.
  • 12. The ABO blood types result from codominant alleles.
  • 13.
  • 14.
  • 15. The sex of sea turtles depends on both genes and the environment
  • 16.
  • 17. Mutant Wild type Gene linkage was explained through fruit flies. Morgan found that linked traits are on the same chromosome. Chromosomes, not genes, assort independently during meiosis.
  • 18.
  • 19.
  • 20. gene A and gene B cross over 6.0 percent of the time
  • 21. gene B and gene C cross over 12.5 percent of the time
  • 22.
  • 23. Human genetics follows the patterns seen in other organisms. The basic principles of genetics are the same in all sexually reproducing organisms. Inheritance of many humantraits is complex. Single-gene traits areimportant in understandinghuman genetics.
  • 24. Y X Females can carry sex-linked genetic disorders. Males (XY) express all of their sex linked genes. Expression of the disorder depends on which parent carries the allele and the sex of the child.
  • 25. A pedigree is a chart for tracing genes in a family. Phenotypes are used to infer genotypes on a pedigree. Autosomal genes show different patterns on a pedigree than sex-linked genes.
  • 26.
  • 27.
  • 28. deletion of part of a chromosome or loss of a chromosome
  • 29. large changes in chromosomes
  • 30. extra chromosomes or duplication of part of a chromosome