Pedigree Charts The family tree of genetics Pedigree Charts I II III.

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Presentation transcript:

Pedigree Charts The family tree of genetics

Pedigree Charts I II III

Overview I. What is a pedigree? a. Definition b. Uses II. Constructing a pedigree a. Symbols b. Connecting the symbols III. Interpreting a pedigree

What is a Pedigree?  A pedigree is a chart of the genetic history of family over several generations.  Scientists or a genetic counselor would find out about your family history and make this chart to analyze.

Constructing a Pedigree  Male  Female

Connecting Pedigree Symbols  Fraternal twins  Identical twins Examples of connected symbols:

Connecting Pedigree Symbols  Married Couple  Siblings Examples of connected symbols:

Example  What does a pedigree chart look like?

Symbols in a Pedigree Chart  Affected  X-linked  Autosomal carrier  Deceased

Interpreting a Pedigree Chart 1. Determine if the pedigree chart shows an autosomal or X-linked disease. –If most of the males in the pedigree are affected the disorder is X-linked –If it is a 50/50 ratio between men and women the disorder is autosomal.

Example of Pedigree Charts  Is it Autosomal or X-linked?

Answer  Autosomal

Interpreting a Pedigree Chart 2. Determine whether the disorder is dominant or recessive. –If the disorder is dominant, one of the parents must have the disorder. –If the disorder is recessive, neither parent has to have the disorder because they can be heterozygous.

Example of Pedigree Charts  Dominant or Recessive?

Answer  Dominant

Example of Pedigree Charts  Dominant or Recessive?

Answer  Recessive

Summary  Pedigrees are family trees that explain your genetic history.  Pedigrees are used to find out the probability of a child having a disorder in a particular family.  To begin to interpret a pedigree, determine if the disease or condition is autosomal or X-linked and dominant or recessive.

Pedigree Chart -Cystic Fibrosis

Human Genetics

Karyotype

Chromosome Number  Different # for different species  Full set = 2N=Diploid  N=  # pairs  1 pair from mother  1 pair from father  Humans= 23 pairs or  46 total Homologous Chromosomes are the sets of each pair

Autosomes & Sex Chromosomes Autosomes = # for all traits except sex Sex chromosomes= Pair # 23 XX(female) or XY(male)

Down Syndrome= 3 of #21

Klinefelter’s = XXY