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SPONGE 4. What is the difference between incomplete dominance and codominance ? (7.2) Give an example of each. In incomplete dominance , neither allele is completely dominant nor completely recessive. +. =. Codominant alleles will both be completely expressed. +. =.
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SPONGE 4 What is the difference between incomplete dominance and codominance? (7.2) • Give an example of each
In incomplete dominance, neither allele is completely dominant nor completely recessive. + = Codominant alleles will both be completely expressed. + = The flower will show both red and white
7.4 Human Genetics and Pedigrees 2.1 Atoms, Ions, and Molecules Set up Cornell Notes on pg. 91 • Topic: 7.4 Human Genetics and Pedigrees • Essential Questions: • Don’t forget to add it to your T.O.Contents!
KEY CONCEPT A combination of methods is used to study human genetics.
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. • Ex: widow’s peak Widow’s peak
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.
A pedigree is a chart for tracing genes in a family. • Phenotypes are used to infer genotypes • Autosomal genes show different patterns on a pedigree than sex-linked genes. Widow’s peak No Widow’s peak
Boxes = males Circles = females Shaded = they show the trait White = does not show trait Half shaded = carrier
How many females are in this family? • How many carriers? • How many children were in generation two? • How many offspring in generation three are affected by the trait? Generation 1 Generation 2 Generation 3 Generation 4
Sponge 6 • How many females are in this family? 11 • How many carriers? 7 • How many children were in generation two? 5 • How many offspring in generation three are affected by the trait? 2 Generation 1 Generation 2 Generation 3 Generation 4
If the phenotype is more common in males, the gene is likely sex-linked (meaning the trait is on the X chromosome). Ex: Color blindness males females
Please draw a pedigree chart: Mary and Joe were married in 1912. Joe had a Widow’s Peak (Ww) which is dominant, while Mary did not have a Widow’s Peak (ww) They had two children: A son named Pete who had a Widow’s Peak and a girl named Isabel who did not have a Widow’s Peak. Pete married a woman who was homozygous for a Widow’s Peak (WW), but their daughter Isabel never married. Pete and his wife had three boys. Do his boys have Widow’s Peaks?
Joe Mary Ww ww Isabel Pete Ww WW ww
X Y • A karyotype is a picture of all chromosomes in a cell.
Karyotypes can show changes in chromosomes. • deletion of part of a chromosome or loss of a chromosome • large changes in chromosomes • extra chromosomes or duplication of part of a chromosome
In down syndrome a person has an extra copy of chromosome 21. • In Klinefelter’s syndrome a male has an extra X (XXY).