1. Humans have 23 pairs of chromosomes. One pair of chromosomes is related to the sex of an individual, these chromosomes are called sex chromosomes

2. The other 22 pairs of chromosomes are called autosomes (1-22)

4. Genes that are located on the X chromosome are called sex-linked genes. Traits determined by sex-linked genes are called sex-linked traits (c = colorblind, C = normal) Ex. Color blindness female X c X c male X c Y

5. Sex linked traits are recessive, this means both x chromosomes must have the gene in order for the trait to be expressed.

6. If only one x chromosome is present (in males)and has the sex linked gene, then the trait will be expressed

7. A carrier is a person that has the trait on only one chromosome and does not express the trait. Carriers of sex linked traits are always women. (C= normal, c= colorblind) Ex. Color blind carrier X C X c

9. A colorblind male marries a normal female. What are the offspring genotypes and phenotypes? (C = normal, c = colorblind) X c Y X C

10. A normal male (not colorblind) marries a carrier. What are the offspring genotypes and phenotypes? X C Y X C X c

11. A normal male (not colorblind) marries a colorblind female. What are the offspring genotypes and phenotypes? X C Y X c

12. Hemophilia is characterized by uncontrolled bleeding It is a sex linked disorder caused by errors in the DNA that codes for the proteins involved in clotting

13. Linked Genes Some traits seem to be inherited together. –Example Gray bodied fruit flies also have long wings. Genes that tend to be inherited together are on the same chromosome and called Linked Genes.

14. Mutations Germ-Cell Mutations are changes in your sex cells. They do not affect the person, but can be passed on. Somatic- Cell Mutations are changes to your body cells and can affect you.

15. Mutations A Chromosome Mutation is a change in the structure of a chromosome or the loss or gain of a chromosome. Four main types of mutation. –Deletion –Inversion –Translocation –Duplication

16. Mutations Deletion: The loss of a piece of a chromosome due to breakage. Inversion: a chromosomal segment breaks off flips around backwards and reattaches.

17. Mutations Translocation: A piece of a chromosome breaks off and reattaches to a non homologous chromosome. Duplication: A certain section of the chromosome gets copied twice.

18. Mutations Another mutation that can occur is when sister chromatids fail to separate correctly during meiosis. This is called Non- disjunction.

19. Chromosome Map Scientists are able to locate individual genes on a chromosome. Due to chromosome mapping scientists are able to tell if certain genes are damaged and the resulting disorder.

20. Pedigrees Some Mutations are inherited. Scientists can use Pedigrees to show how a trait is inherited over generations.