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Chapter 14: Human Heredity
Lab Biology CP
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Chapter 14: Human Heredity
14.1 Human Chromosomes 14.2 Human Genetic Disorders 14.3 Studying the Human Genome
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14.1 Human Chromosomes
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What is a genome? A full set of genetic information that an organism carries in its DNA
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Types of Human Chromosomes
Sex chromosomes: pair 23 Autosomes: pairs 1-22 Male: XY Female: XX
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Karotypes Shows the complete diploid set of chromosomes grouped together in pairs, arranged in order of decreasing size
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Normal Male
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Transmission of Human Traits
1. Dominant & Recessive Alleles MC1R gene: helps determine skin and hair color 2. Codominant Alleles and Multiple Alleles Example: blood type 3. Sex-Linked Inheritance Example: color blindness
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Pedigree
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14.2 Human Genetic Disorders
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From Molecule to Phenotype
A small change in DNA sequence can change proteins by altering their amino acid sequences, which may directly affect one’s phenotype.
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Disorders Caused by Individual Genes
Sickle Cell Disease Cystic Fibrosis Huntington’s Disease
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Cystic Fibrosis
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Chromosomal Disorders
Caused by an extra or missing chromosomes Example: Trisomy 21 (Down’s Syndrome) Extra 21st chromosome
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Trisomy 21 Karyotype
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14.3 Studying the Human Genome
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Techniques used to study DNA
Cutting DNA with restriction enzymes Separating DNA fragments by gel electrophoresis Reading DNA with dye-labeled nucleotides
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Cutting DNA
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Reading DNA
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Separating DNA
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The Human Genome Project
Human Genome mapped by the U.S. and other countries February 2001 completed Took 13 years to complete Sequenced all 3 billion base pairs
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