Heredity in Deafness Rachel Malinowski Christine Keogh Jon Bordogna Melissa Snyder.

Slides:



Advertisements
Similar presentations
Genetics. Cells-Nucleus-Chromosomes- DNA- Genes They are all found in a cell. They are all located in the body.
Advertisements

Medical Mystery Patient X. Symptoms 0 Patient’s Symptoms: 0 Possible Diseases/Disorders: 0 Final Diagnosis:
Chromosome Disorders. Classification of genetic disorders  Single-gene disorders (2%)  Chromosome disorders (
Vocabulary Review Ch 12 Inheritance Patterns and Human Genetics.
Genetics Jeopardy Mendel’s WorkProbability and Heredity The Cell and Inheritance The DNA Connection Miscellaneous
Introduction to Human Genetics. Facts Humans have 46 chromosomes or 23 pairs of chromosomes 2 types of chromosomes: –Autosomes: chromosomes that determine.
Mutations Section 12–4 This section describes and compares gene mutations and chromosomal mutations.
DNA – Chromosomes - Genes. DNA DNA: the chemical inside the nucleus of a cell that carries the genetic instructions for making living organisms. The material.
Single-gene Disorders. Classification of genetic disorders  Single-gene disorders (2%)  Chromosome disorders (
Mutations and other genetic issues
Chapter 4, Section 2 Human Genetic Disorders
 What is genetics?  Genetics is the study of heredity, the process in which a parent passes certain genes onto their children. What does that mean?
12.4 MUTATIONS I. Kinds of Mutations
C HAPTER 6: G ENETIC DISEASES. I NTRODUCTION Cystic fibrosis:
Inheritance Patterns and Human Genetics. Sex Chromosomes and Autosomes Sex Chromosomes contain genes that determine the gender of an individual. Many.
Let’s think about it… What are autosomes? What are sex chromosomes?
DNA and Genetics Jeopardy Review Game. $2 $5 $10 $20 $1 $2 $5 $10 $20 $1 $2 $5 $10 $20 $1 $2 $5 $10 $20 $1 $2 $5 $10 $20 $1 Transcription &Translation.
Genetics Chapter Twelve: The Code of Life 12.1 The Role of DNA in Heredity 12.2 DNA and Technology.
Chapter 11 DNA and GENES. DNA: The Molecule of Heredity DNA, the genetic material of organisms, is composed of four kinds nucleotides. A DNA molecule.
12-4 Mutations Objective: Contrast gene mutations & chromosomal mutations Are all mutations bad?
Heredity and Variation SOL Review. Which of these is NOT the result of genetic mutations? A. Downs syndrome B. sickle - cell anemia C. green eyes.
Mutations Learning Targets: Describe different gene mutations.
Genetics. Genetics is the study of the inheritance of Characteristics Which of the following do you think are characteristics? Hair colour Eye Colour.
Human Heredity. A karyotype is a picture of chromosomes Of the 46 human chromosomes, they are arranged in 23 pairs 22 of the pairs are called body chromosomes.
Genetic Disorders. Caused by a harmful mutation (physical change of gene) Mutation originally occurs in gamete and is passed to future generations (inherited)
Genetics Jeopardy Terms Central Dogma MutationsStructuresMolecular.
How Does DNA Control Traits? Lesson 3 pg. A52 Ms. Lourdes Martinez 6th Grade.
Heredity and Genetics (2:39) Click here to launch video Click here to download print activity.
Chromosomes, DNA, and Genes EQ: Can I describe the relationship among genes, chromosomes, and inherited traits?
Chapter 2 Your Heredity.  Chromosomes  Where heredity information is stored  Gene  The basic unit of heredity  Dominant gene  The more influential.
Slide 1 of 24 VIII MUTATIONS Mutations Types of Mutations:
End Show Slide 1 of 24 Copyright Pearson Prentice Hall 12-4 Mutations Outline 12–4: Mutations.
Similarities Cells-Nucleus- Chromosomes- DNA- genes Cells-Nucleus-Chromosomes- DNA- genes They are all located in cells.
Mutations (p. 307) Mutations are changes in the genetic material. Mutations may be genetic mutations or chromosomal mutations.
4.12 DNA and Mutations. Quick DNA Review Base pairing Base pairing.
DNA AND GENETICS Chapter 12 Lesson 3. Essential Questions What is DNA? What is the role of RNA in protein production? How do changes in the sequence of.
Objective: To discuss different mutations Gene mutation Mutations: change in genetic material Gene Mutation: change is on one or a few nucleotides.
Genetics Test Review Mrs. Callan Biology 2017.
GENES, MUTATIONS & DISEASES:
MUTATIONS Where, when, why, and how?.
T. Trimpe Genetics Challenge #4 T. Trimpe
Genetics and Heredity.
Down Syndrome By Todd Martorano.
12.4 Mutations Changes in the genetic material
MUTATIONS.
Mutations Changes in the genetic material Gene Mutations
what are autosomes? What are sex chromosomes?
Heredity and Genetic Mutations
Genes and Traits review
Kinds of Mutations Point Mutation Occur at a single point in the DNA
Name of the disorder.
Unit 2.2 RELATIONSHIP BETWEEN DNA, CHROMOSOMES AND GENES
Mutations Chapter 9.
Genetics – The study of Inheritance
Human Genetic Disorders
Topic #3: Types of Mutations
HUMAN HEREDITY.
MUTATIONS.
Gene and Chromosomal Mutations
Autosomal dominant inheritance: the basics
The role of DNA in heredity
MUTATIONS.
S3: HEREDITY E6: KARYOTYPES
Mutation Notes.
Objective: Explain the main types of mutations
Definition Here Vocabulary Word Here Definition Here
Mutations.
CHAPTER 11 GENETICS Genetics is the study of how traits or characteristics are inherited. Inherited characteristics are controlled by genes and are passed.
Inheritance & Variance Traits Vocabulary
Copyright Pearson Prentice Hall
Presentation transcript:

Heredity in Deafness Rachel Malinowski Christine Keogh Jon Bordogna Melissa Snyder

Facts n 1 in 2,000 children are born deaf n Deafness can occur by itself or as part of a syndrome n Over 28 million Americans are deaf n Deafness is caused by over 100 genetic disorders n Recessive inheritance is most common form of genetic deafness, accounting for approx. 80% of inherited deafness

Causes n Multi-gene trait--no obvious difference between deafness caused by different genes, so finding the genes involved is very difficult. Some Examples Are….

–chromosome 5q31 n single nucleotide substitution leading to a four- base pair insertion in messenger RNA and a frameshift. –Mutation: 1555(12s rRNA)7445(tRNA serine) n Mitochondrial DNA, only inherited from mother. n Changes in Mitochondrial DNA deafness explains 1% of genetic deafness. –Gene KCNQ1 and KCNQ4 n prevents secretion of potassium into the fluid that surrounds sensory cells of the ear. –Dominant Autosomal Deafness (DFNA) n Appears late in life, develops slowly

Autosomal Dominant - 5q I II III