Pedigree Used to show how a particular trait is passed from one generation to the next in a family.

Slides:



Advertisements
Similar presentations
Human Inheritance Notes Ch Part II
Advertisements

14.1 Human Chromosomes What makes us human? What makes us different from other animals such as a chimpanzee? About 1% of our DNA differs from a chimp.
6.2 Human Genetic Disorders
 What’s a “mutagen”?  What does a mutation do to DNA?  If a mutation affects a gene, then what might happen to the protein sequence?
Human Genetic Disorders
Chapter 12: Patterns of Heredity & Human Genetics
6-2 Human Genetic Disorders
Human Genetics.
List at least 3 genetic conditions you know of. Why do you think they are genetic conditions?
Human Genetics Chapter 14 in the Textbook.
INHERITED GENETIC DISORDERS
Pedigree definition  Pedigree: a family history that shows how a trait is inherited over several generations  Pedigrees are usually used when parents.
This type of genetic disorder requires both parents to “donate” a defective gene.
Chapter 12.  Humans have 46 chromosomes  44 are autosomes  22 pairs of homologous chromosomes  2 are sex chromosomes: X and Y  Females have two X.
SEX DETERMINATION The sex of an individual is determined by the sex chromosomes contributed to the zygote by the sperm and the egg.
Chapter 14 Human Chromosomes Karyotype: a picture of the chromosomes from a single cell. Used to determine the sex, or possible genetic disorders of.
Wake-up 1.A woman carrying hemophilia marries a man who is a hemophiliac. What percentage of their children will have hemophilia? 1.Cross a man heterozygous.
Genetic Disorders.
You already know… - A chromosome is a structure that carries genetic information Each cell normally has 23 pairs of chromosomes: 1 pair of sex chromosomes.
Human Heredity  This section explains what scientists know about human chromosomes, as well as the inheritance of certain human traits and disorders.
Human Genetics: Patterns of Inheritance for Human Traits.
Human Genetic Disorders
Tracing the Inheritance of the Human Y Chromosome
ABO Blood Groups and Genetic Disorders
Genetics Part 3 Modes of Inheritance
Genetic Disorders  Caused by mutations inherited from a parent  mutations are mistakes that are present in the DNA of virtually all body cells. VideoclipVideoclip.
Thursday 2/2 How many copies of the chromosome for skin color do you have? Why do you have that many? What is similar and what is different about the.
Human Inheritance. Review – What is Heredity? Heredity is the passing of traits from parents to offspring Genes are passed from parents to offspring (**Remember.
Genetics. Color Blindness w Occurs more frequently in men w sex-linked (X) w affects light receptors in the eye red/green complete.
Simple Inheritance, Pedigrees, & Karyotypes Pedigrees Similar to family trees graphicA graphic representation of genetic inheritance.
Genetics. Color Blindness w Occurs more frequently in men w sex-linked (X) w affects light receptors in the eye red/green complete.
End Show Slide 1 of 43 Copyright Pearson Prentice Hall 14–1 Human Heredity 14-1 Human Heredity.
Section 4: Complex Patterns of Heredity
Human Genetics: Patterns of Inheritance for Human Traits.
Human Heredity Chapter 14-1, 14-2, 14-3.
Pedigree definition  Pedigree: a family history that shows how a trait is inherited over several generations  Pedigrees are usually used when parents.
Do Now Incomplete or Codominance? Human Genetics: Patterns of Inheritance for Human Traits.
Human Genetics Genetics of sex Women & men are very different, but just a few genes create that difference In mammals = 2 sex chromosomes –X & Y –2 X.
Pedigrees.
What determines are phenotypes? Autosomes- chromosomes 1-44, pairs 1-22 Sex chromosomes- 23 rd pair of chromosomes – Females have two copies of a large.
Chapter 7 Extending Mendelian Genetics. Karyotype = picture of all chromos in cell They can show a change in chromos whether autosomal or sex-linked.
Human Genetic Disorders
Genetic Diseases & Disorders Biology Huntington’s disease-- lethal genetic disorder resulting in a breakdown in areas of the brain. Onset occurs between.
Today’s Agenda…  Bellringer: Life Science Multiple Choice Questions  Discuss homework from last night  Notes on Human Genetic Disorders.
Karyotypes and Pedigrees Inheritance of Genetic Traits.
GENETIC MUTATIONS. DNA and Mutations Mutations are any changes that take place in DNA: Can change the genetic code, and be replicated when forming new.
Human Genetic Disorders Notes. What causes genetic disorders? Mutations, or changes in a person’s DNA.
Welcome 2/10-11/16 1. Turn in Quick Lab and Dihybrid Cross 2. Other Mendelian Genetics and Disorders Notes 3. Practice Non-Mendelian Genetics.
11.1 Basic Patterns of Human Inheritance Complex Inheritance and Human Heredity Chapter 11 Recessive Genetic Disorders  A recessive trait is expressed.
Common Genetic Disorders. Cystic Fibrosis Recessive Facts: mucus in lungs & digestive tract is very thick ; caused by point mutation Symptoms: makes breathing.
Section 2 Human Genetic Disorders. 1 st three terms…also in next 3 slides! Genetic disorder - an abnormal condition that a person inherits through genes.
Chapter 14 Human Heredity. Human Chromosomes A picture of chromosomes arranged in this way (previous page) is know as a karyotype. This karyotype is.
Genetic Diseases & Disorders Biology Genetics Diseases outline Dominant 1. Huntington’s Recessive 1. Cystic fibrosis 2. Sickle-cell anemia 3. Tay-Sachs.
The Human Genome Chapter 14 – Human Heredity Human Chromosomes.
Basic Patterns of Human Inheritance Complex Inheritance and Human Heredity Section 1 Recessive Genetic Disorders  A recessive trait is expressed when.
Genetic Disorders Cystic Fibrosis
HUMAN TRAITS. PEDIGREE * CHART OF RELATIONSHIPS WITH A FAMILY; DETERMINES GENOTYPES OF TRAITS OF MEMBERS.
Genetic disorders. SICKLE CELL ANEMIA CODOMINANT RBC appear sickle-shaped and reduced ability to carry oxygen The 11th pair of chromosomes contains a.
Inherited Genetic Disorders & Pedigrees
The Human Genome Chapter 14.
ABO Blood Groups and Genetic Disorders
Human Genetics By Diana Bivens.
Genetic Disorders.
Human Heredity.
The Human Genome Chapter 14.
INHERITED GENETIC DISORDERS
Genetic Disorders.
GENETIC DISORDERS.
Presentation transcript:

Pedigree Used to show how a particular trait is passed from one generation to the next in a family

Allelic Disorders - genetic disorders are USUALLY recessive

Albinism Many forms, many genes code for it Lack of pigment in skin, hair, and eyes. Approx. 1 in 17,000 people Health Impacts 1.Eye problems 2.Severe sensitivity to sunburn.

Cystic Fibrosis Gene mutation on chromosome 7 Health: build up of mucus in the lungs, pneumonia One of the first disorders to be actively studied for gene therapy.

Sickle Cell Anemia Codominant disorder found in African Americans. Red blood cells are mishapen. Characterized by extreme pain in legs and arms because the cells get stuck in capillaries.

Tay-Sachs Fatal genetic disorder from a buildup of fatty substances in tissues and nerve cells in brain. Infants develop normally then deteriorate to become blind, deaf, unable to swallow leading to muscle atrophy and paralysis. Persons with Tay-Sachs also have "cherry-red" spots in their eyes. Both parents must carry the mutated gene in order to have an affected child.

Huntington’s Disease Results in a loss of muscle control and mental function. The symptoms usually do not appear until after 30 years old. Approximately 1 in 10,000 births Gene on chromosome 4

Huntington’s Disease

Color Blindness Recessive gene located on the X chromosome. Sex-Linked disorder Cannot distinguish red/green Does color blindness affect more men or women? MEN Why? Men only have one X chromosome, thus only one copy of the color blind gene.

Hemophilia A disorder in which a person’s blood does not clot properly. Gene found on X chromosome. 1 in 10,000 males born are afflicted.

Pedigree Chart and Symbols