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.

Slides:



Advertisements
Similar presentations
CH 14.1 Human Heredity.
Advertisements

Two copies of each autosomal gene affect phenotype.
6.2 Human Genetic Disorders
Introduction to Human Genetics. Facts Humans have 46 chromosomes or 23 pairs of chromosomes 2 types of chromosomes: –Autosomes: chromosomes that determine.
Human Heredity.
Human genetic disorders
Human Genetics EQ: How can genetic patterns be analyzed to determine dominant or recessive inheritance patterns?
Human Heredity Section 14–1
Heredity Chapter 29. Genetics Terminology Chromosome Homologous Chromosome Autosomal chromosomes Sex chromosomes Gene.
The Human Genome Chapter 14 Donna Howell Biology I Blacksburg High School.
Human Genetics Chapter 12.
Human Heredity Sections 14-1 and 14-2 Objectives: 7.2 Interpreting inheritance patterns shown in graphs and charts 8.5 Relating genetic disorders and disease.
Chapters 13 and 14 Genetic Engineering, The Human Genome.
Chapter 7 PowerPoint by Jacob Rondinella.
Human Heredity 11.3 Human Chromosomes Humans have 46 chromosomes Occurs in 23 pairs 22 pairs are autosomes 2 of the 46 are sex-determining chromosomes.
End Show Slide 1 of 43 Copyright Pearson Prentice Hall 14–1 Human Heredity 14-1 Human Heredity.
A. albinism B. cystic fibrosis C. galactosemia D. Tay-Sachs 1. Identify the disease characterized by the absence of melanin. Complex Inheritance and Human.
Human Heredity Chapter 14-1, 14-2, 14-3.
What is genetics? 01. Genetics is the study of inherited traits.
Chapter 14 - The Human Genome
Chromosomal Disorders. Non-disjunction During meiosis, chromosomes are supposed to be divided evenly and into gametes. During meiosis, chromosomes are.
Ch 6, Sec 2 Human genetic disorders
Human Genome Biology Ch 14.
Human Genome. Karyotype – a picture of a cell’s chromosomes group in homologous pairs Humans have 46 chromosomes Two of these are sex chromosomes (XX.
JUST DISORDERS. What disorder is it? Mutation in the blood clotting protein makes person unable to stop bleeding after an injury _______________ Mutation.
Genetic Disorders & Chromosomal Mutations Chapter 12.
Mendelian Inheritance
Genetic Disorders. Caused by a harmful mutation (physical change of gene) Mutation originally occurs in gamete and is passed to future generations (inherited)
The Human Genome Ch. 14. Human Chromosomes Karyotype = how chromosomes are arranged in pairs Humans have 46 chromosomes or 23 pairs The 23 rd pair are.
Ch. 14: Human Heredity Essential questions: How is blood type inherited? How is blood type inherited? What is a sex-linked trait? What is a sex-linked.
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 disorders can be due to any of the following factors: A. Monogenetic Disorders: Caused by a mutation in a single gene 1. Autosomal recessive alleles:
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.
11.1 Basic Patterns of Human Inheritance Complex Inheritance and Human Heredity Chapter 11 Recessive Genetic Disorders  A recessive trait is expressed.
Ch. 14 The Human Genome.
Chap 6 notes Human Inheritance. Karyotype Shows all 46 human chromosomes 23 pairs Chromosomes 1-22 are autosomes (regular chromosomes) The last set of.
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.
1 Chapter 14- Human Genome Students know why approximately half of an individual ’ s DNA sequence comes from each parent. Students know the role of chromosomes.
HUMAN TRAITS. PEDIGREE * CHART OF RELATIONSHIPS WITH A FAMILY; DETERMINES GENOTYPES OF TRAITS OF MEMBERS.
Lesson Overview Lesson Overview Human Chromosomes Objectives 14.1 Human Chromosomes - -Identify the types of human chromosomes in a karotype. -Describe.
Human Genetics.
A picture of chromosomes in ordered pairs
Chapter 14: Human Heredity
Human Genetic Disorders
Chapter Seven: Extending Mendelian Genetics
Human Heredity.
Chapter 14 Human Genetics.
Human Genetics EQ: How can genetic patterns be analyzed to determine dominant or recessive inheritance patterns?
When Something Goes Wrong…
Mendelian Inheritance of Human Traits
Chapter 14 Human Heredity.
Human Genetics Human Genetics.
Chapter 14- Human Genome Students know why approximately half of an individual’s DNA sequence comes from each parent. Students know the role of chromosomes.
Pedigree Notes.
Pedigree Notes.
Karyotypes.
The Human Genome Ch. 14.
Unit 6 “Complex Inheritance”
Human Heredity.
14.1 – Human Heredity.
Copyright Pearson Prentice Hall
Pedigree tips for autosomal genetic diseases Determine whether the trait of interest is dominant (A) or recessive (a) Label the genotypes.
S3: HEREDITY E6: KARYOTYPES
Patterns of Heredity & Human Genetics
Key Concepts What are two major causes of genetic disorders in humans?
Human Inheritance Test Review
Methods of inheritance
Genetic Disorders & Chromosomal Mutations
Presentation transcript:

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 (called autosomes) One of the pairs are the sex chromosomes (x and/or y)

A pedigree chart can be used to represent heredity in a family

Dominant Disorders Huntington's

Codominant Disorders Sickle Cell

Recessive Disorders Albinism Cystic fibrosis – chromosome 7 recessive allele PKU (phenylketonuria) Tay-Sachs

Down Syndrome Person has an extra copy of chromosome 21 (3 copies)

Blood Typing Blood type is controlled by a single gene with three alleles