HUMAN TRAITS. PEDIGREE * CHART OF RELATIONSHIPS WITH A FAMILY; DETERMINES GENOTYPES OF TRAITS OF MEMBERS.

Slides:



Advertisements
Similar presentations
Section 1: Basic Patterns of Human Inheritance
Advertisements

Chapter 12 Patterns of Heredity and Human Genetics
Notes: Types of Inheritance
 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?
Chapter 12: Patterns of Heredity & Human Genetics
Human Heredity.
 FOLLOWING PATTERNS OF INHERITANCE. Humans cannot undergo breeding experiments for use in genetic studies – ethical implications.
Human Genetics Chapter 14 in the Textbook.
Human Heredity Section 14–1
BIOLOGY BINGO GENETICS. HemophiliaDominant Color-blindnessCarrier Cystic fibrosisPKU Tay-sachsHuman blood Klinfelters syndromeGenetics Sickle cell anemiaAlleles.
Section 2 Human Genetics Chapter 12 Objectives Analyze pedigrees to determine how genetic traits and genetic disorders are inherited. Summarize the different.
This type of genetic disorder requires both parents to “donate” a defective gene.
Genetic Disorders.
Human Genetics Review – What is a GENE? A gene is the unit that controls traits Genes are passed from parents to offspring Genes are located on our chromosomes.
Human Genetics Chapter 12.
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.
Simple Inheritance, Pedigrees, & Karyotypes Pedigrees Similar to family trees graphicA graphic representation of genetic inheritance.
End Show Slide 1 of 43 Copyright Pearson Prentice Hall 14–1 Human Heredity 14-1 Human Heredity.
Pedigree Used to show how a particular trait is passed from one generation to the next in a family.
Jumpstart 12/5 1. Gametes: For each of the genotypes presented below, determine all of the possible haploid gametes. For each of the genotypes presented.
 Genetic Family Tree  Maps only one trait at a time.
Human Heredity Chapter 14-1, 14-2, 14-3.
Testcross Dominant phenotype with unknown genotype Recessive phenotype
Human Genome Biology Ch 14.
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.
Human Genetic Disorders Two Types: Autosomal Recessive Disorder – Most common type, only shows in the phenotype when genotype is homozygous recessive.
Genetic Disorders By: Tanner and Jack.
Mendel and Human Traits. Mendelian Inheritance Heterozygous and Homozygous Dominant have the same phenotype Homozygous recessive will have a different.
Pedigrees.
Chapter 7 Extending Mendelian Genetics. Karyotype = picture of all chromos in cell They can show a change in chromos whether autosomal or sex-linked.
Patterns of Heredity and Human Genetics.  Pedigree – made up of a set of symbols that identify males and females, the individuals affected by a trait.
PEDIGREES (12.3) * a chart that shows how a trait and the genes that control it are inherited within a family. Symbols: female male mate/ marriage offspring.
Pedigrees & Pattern of Gene Inheritance. Target #19- I can describe the layout & purpose of a pedigree Many human disorders are genetic in origin  Genetic.
11.1 Basic Patterns of Human Inheritance Complex Inheritance and Human Heredity Chapter 11 Recessive Genetic Disorders  A recessive trait is expressed.
Basic Patterns of Human Inheritance Copyright © McGraw-Hill Education Recessive Genetic Disorders A recessive trait is expressed when the individual is.
Chapter 14 Human Heredity. Human Chromosomes A picture of chromosomes arranged in this way (previous page) is know as a karyotype. This karyotype is.
The Human Genome Chapter 14 – Human Heredity Human Chromosomes.
Sex-Linked Traits. Inheritance of Traits  X-linked Disorders - occur mainly in males because the mother usually donates the recessive allele and males.
Genetic Disorders Cystic Fibrosis
GENETICS REVIEW QUESTIONS WITH ANSWERS. 1. The passing on of traits from parent to offspring is called…… ?? 2. The gamete that contains genes contributed.
1 Chapter 12 College Prep Biology Patterns of Heredity & Human Genetics.
Chapter Seven: Extending Mendelian Genetics
Heredity and Genetics Chapter 12.1.
Basic Patterns of Inheritance
Human Genetics By Diana Bivens.
Human Heredity.
Genetics.
Mendelian Inheritance of Human Traits
Section Objectives: Interpret a pedigree.
Chapter 14.1 Human Heredity.
How can human traits be traced through generations?
GENETICS AND HEREDITY.
Sexually reproducing organisms have two of each chromosome.
& Human Heredity January 6th/7th, 2008
Additional Punnette Squares
14.1 – Human Heredity.
Human Genetics.
Simple Dominant Traits
Pedigree tips for autosomal genetic diseases Determine whether the trait of interest is dominant (A) or recessive (a) Label the genotypes.
Complex Inheritance and Human Heredity
GENETIC DISORDERS.
Chapter 10 assessment.
Methods of inheritance
Human Genetics.
Patterns of Heredity and Human Genetics
Chapter 14 The Human Genome.
Types of Inheritances I Pp , 244
Complex Patterns of Inheritance
Presentation transcript:

HUMAN TRAITS

PEDIGREE * CHART OF RELATIONSHIPS WITH A FAMILY; DETERMINES GENOTYPES OF TRAITS OF MEMBERS

Autosomal Recessive Diseases Inheritance when 2 parents who share a recessive gene for a disease pass this gene to an offspring. Usually, parents are heterozygous for this trait & are unaware of their potential for passing on this disease. Examples: Tay-Sachs Disease, Albinism, Cystic Fibrosis, PKU

RECESSIVE ALLELE DISORDERS 1. ALBINISM (aa) = NO SKIN PIGMENT

2. CYSTIC FIBROSIS – EXCESS LUNG MUCUS

3. PKU –HIGH PHENYLALANINE (AMINO ACID) IN TISSUES.

4. TAY-SACHS – HIGH LIPIDS IN BRAIN

AUTOSOMAL DOMINANT DISORDERS *the inheritance of a single copy of a defective gene that “over-rides” normal gene !

1. HUNTINGTON’S DISEASE – NEUROLOGICAL

CO-DOMINANT DISORDERS 1. SICKLE-CELL DISORDER – RED BLOOD CELLS