Genetics test review
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This document contains multiple genetics questions about inheritance patterns in humans and other organisms. It asks the reader to determine expected phenotypic and genotypic ratios from given crosses, identify parental genotypes, and assign alleles to explain observed inheritance patterns. It also contains basic questions about genetics concepts like the number of chromosomes per cell and the definition of a gene.
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This document summarizes key concepts about heredity and genetics covered in Chapter 5, including:
1) Heredity is the passing of traits from parents to offspring through alleles contained in DNA. Gregor Mendel studied heredity through pea plant experiments.
2) Mendel discovered dominant and recessive traits and that recessive traits can reappear through cross-breeding.
3) Punnett squares are used to determine the probability of traits being passed down based on parental genotypes.
4) Other concepts covered include incomplete dominance, multiple alleles, polygenic inheritance, mutations, sex determination, and genetic engineering techniques.
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The document discusses genes, DNA, RNA, heredity, and reproduction. It defines a gene as the unit of heredity that contains DNA instructions for an organism's traits. DNA encodes genetic instructions and is made up of nucleic acids alongside proteins and carbohydrates. RNA also contains genetic codes and has various biological roles. Heredity is the passing of traits from parents to offspring via sexual or asexual reproduction. The two types of reproduction are sexual, which combines genetic material from two parents, and asexual, which involves one parent. Genes hold the codes to build and maintain organisms and are passed down through reproduction.
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The document discusses inheritance patterns and genetic disorders. It provides examples of experiments studying inheritance in pea plants. Mendel's experiments on pea plants showed that offspring inherit traits from parents through alleles and that some alleles are dominant while others are recessive. The document also summarizes several genetic disorders and their inheritance patterns such as diabetes, cancer, heart disease, and PKU. It describes the genetic and environmental factors that influence these conditions.
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The document discusses Gregor Mendel and the foundations of classical genetics. It describes how Mendel studied inheritance patterns in peas in the 1860s. He found that traits are passed through discrete factors (now known as genes) and that some traits are dominant while others are recessive. His work established the laws of segregation and independent assortment. He demonstrated that alleles separate and are transmitted independently, allowing for prediction of inheritance patterns.
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The document discusses genetics and patterns of inheritance. It defines genetics as the study of heredity and how traits are passed from parents to offspring through mechanisms like meiosis and fertilization. It also defines heredity, variation, and mutation. The document then discusses Gregor Mendel's experiments with pea plants in the 1860s, where he studied inheritance of traits like seed shape, pod shape, and flower color. His experiments led to the formulation of Mendel's laws of inheritance - the law of dominance, the law of segregation, and the law of independent assortment.
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This document discusses several patterns of inheritance including:
1. Dominant and recessive genes and how they determine traits like coat color in mice.
2. Lethal alleles that cause death in homozygous dominant genotypes.
3. Incomplete dominance and codominance where both alleles are partially or fully expressed.
4. Sex linkage and how traits on the X chromosome are inherited differently between males and females.
It also discusses environmental influences on gene expression and abnormal chromosome numbers leading to conditions like Down syndrome.
Human genetic inheritance patterns
The document discusses 5 patterns of human inheritance: complete dominance, incomplete dominance, co-dominance, sex-linked traits, and polygenic traits. It provides examples for each pattern including Mendelian genetics (BB, Bb, bb), blending of traits in flowers, expression of both parental alleles in horses, traits on the X/Y chromosomes, and traits influenced by multiple gene pairs like hair/eye color. The document also describes how karyotypes and pedigree charts are used to study inheritance in families by examining chromosomes and mapping genetic traits through generations.
Recommended
Mendelian - Heredity
About Gregor Mendel's Theory and its application in Science and Health for Grade9 students who are studying Science 9
Chapter 5- Heredity
This document summarizes key concepts about heredity and genetics covered in Chapter 5, including:
1) Heredity is the passing of traits from parents to offspring through alleles contained in DNA. Gregor Mendel studied heredity through pea plant experiments.
2) Mendel discovered dominant and recessive traits and that recessive traits can reappear through cross-breeding.
3) Punnett squares are used to determine the probability of traits being passed down based on parental genotypes.
4) Other concepts covered include incomplete dominance, multiple alleles, polygenic inheritance, mutations, sex determination, and genetic engineering techniques.
Genes and inheritance
The document discusses genes, DNA, RNA, heredity, and reproduction. It defines a gene as the unit of heredity that contains DNA instructions for an organism's traits. DNA encodes genetic instructions and is made up of nucleic acids alongside proteins and carbohydrates. RNA also contains genetic codes and has various biological roles. Heredity is the passing of traits from parents to offspring via sexual or asexual reproduction. The two types of reproduction are sexual, which combines genetic material from two parents, and asexual, which involves one parent. Genes hold the codes to build and maintain organisms and are passed down through reproduction.
Inheritance patterns new
The document discusses inheritance patterns and genetic disorders. It provides examples of experiments studying inheritance in pea plants. Mendel's experiments on pea plants showed that offspring inherit traits from parents through alleles and that some alleles are dominant while others are recessive. The document also summarizes several genetic disorders and their inheritance patterns such as diabetes, cancer, heart disease, and PKU. It describes the genetic and environmental factors that influence these conditions.
Classical Genetics Lecture
The document discusses Gregor Mendel and the foundations of classical genetics. It describes how Mendel studied inheritance patterns in peas in the 1860s. He found that traits are passed through discrete factors (now known as genes) and that some traits are dominant while others are recessive. His work established the laws of segregation and independent assortment. He demonstrated that alleles separate and are transmitted independently, allowing for prediction of inheritance patterns.
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The document discusses genetics and patterns of inheritance. It defines genetics as the study of heredity and how traits are passed from parents to offspring through mechanisms like meiosis and fertilization. It also defines heredity, variation, and mutation. The document then discusses Gregor Mendel's experiments with pea plants in the 1860s, where he studied inheritance of traits like seed shape, pod shape, and flower color. His experiments led to the formulation of Mendel's laws of inheritance - the law of dominance, the law of segregation, and the law of independent assortment.
Patterns of Inheritance
This document discusses several patterns of inheritance including:
1. Dominant and recessive genes and how they determine traits like coat color in mice.
2. Lethal alleles that cause death in homozygous dominant genotypes.
3. Incomplete dominance and codominance where both alleles are partially or fully expressed.
4. Sex linkage and how traits on the X chromosome are inherited differently between males and females.
It also discusses environmental influences on gene expression and abnormal chromosome numbers leading to conditions like Down syndrome.
Human genetic inheritance patterns
The document discusses 5 patterns of human inheritance: complete dominance, incomplete dominance, co-dominance, sex-linked traits, and polygenic traits. It provides examples for each pattern including Mendelian genetics (BB, Bb, bb), blending of traits in flowers, expression of both parental alleles in horses, traits on the X/Y chromosomes, and traits influenced by multiple gene pairs like hair/eye color. The document also describes how karyotypes and pedigree charts are used to study inheritance in families by examining chromosomes and mapping genetic traits through generations.
Pattern of inheritance 01
This document defines key genetic terms and summarizes Mendel's laws of inheritance. It explains that genes determine traits which are passed from parents to offspring. Mendel discovered the laws of dominance, segregation, and independent assortment through his pea plant experiments. The document also outlines different patterns of inheritance such as dominant-recessive, incomplete dominance, co-dominance, sex-linked, and polygenic inheritance. Polygenic traits like skin color are influenced by multiple genes resulting in a continuum of phenotypes.
Human genetics
This document discusses basic concepts in human genetics including genes, chromosomes, DNA, alleles, dominant and recessive traits, and genetic disorders. It covers key topics like the human genome, inheritance from parents, genetic testing methods like amniocentesis and chorionic villus sampling, influences on prenatal development, and genetic counseling.
10. patterns of inheritance
Gregor Mendel's pea plant experiments in the mid-19th century laid the groundwork for genetics by demonstrating that traits are passed from parents to offspring via discrete units of inheritance called genes. The document defines genetic terminology like alleles, genotypes, phenotypes, dominant/recessive traits, and describes Mendel's laws of segregation and independent assortment. It also discusses sex-linked inheritance and variations like incomplete dominance and polygenic traits. Common human genetic disorders are reviewed including examples like sickle cell disease, cystic fibrosis, and Duchenne muscular dystrophy.
1. Genetics and heredity
Genetics is the study of genes, heredity, and variation in living organisms. Genes hold the information to build and maintain an organism. Genes are found within each cell of the body, located on structures called chromosomes within the nucleus. Humans have 23 pairs of chromosomes, with one set inherited from each parent, containing the genes that determine traits like eye color. Differences in genes between individuals result in biological diversity.
Heredity and genetics
Heredity is the passing on of characteristics from one generation to the next. It is the reason why offspring look like their parents. It also explains why cats always give birth to kittens and never puppies. The process of heredity occurs among all living things including animals, plants, bacteria, protists and fungi. The study of heredity is called genetics and scientists that study heredity are called geneticists.
Through heredity, living things inherit traits from their parents. Traits are physical characteristics. You resemble your parents because you inherited your hair and skin color, nose shape, height, and other traits from them.
Cells are the basic unit of structure and function of all living things. Tiny biochemical structures inside each cell called genes carry traits from one generation to the next. Genes are made of a chemical called DNA (deoxyribonucleic acid). Genes are strung together to form long chains of DNA in structures known as chromosomes. Genes are like blueprints for building a house, except that they carry the plans for building cells, tissues, organs, and bodies. They have the instructions for making the thousands of chemical building blocks in the body. These building blocks are called proteins. Proteins are made of smaller units called amino acids. Differences in genes cause the building of different amino acids and proteins. These differences cause individuals to have different traits such as hair color or blood types.
A gene gives only the potential for the development of a trait. How this potential is achieved depends partly on the interaction of the gene with other genes. But it also depends partly on the environment. For example, a person may have a genetic tendency toward being overweight. But the person's actual weight will depend on such environmental factors as how what kinds of food the person eats and how much exercise that person does.
Genetics and inheritance
This document provides an overview of genetics and inheritance concepts taught in Campbell & Reece's chapters 14 and 15. It summarizes Mendel's experiments with pea plants which established the basic principles of heredity, including dominant and recessive traits, genotypes and phenotypes, monohybrid and dihybrid crosses. It also covers sex determination, sex-linked inheritance, degrees of dominance, and polygenic inheritance. Mendel's work laid the foundation for genetics as a scientific field.
Classical genetics
Here are the answers to the seatwork:
1. AA - Homozygous
2. Rr - Heterozygous
3. aaBB - Two pairs that are homozygous
4. MmNN - Two pairs that are heterozygous
5. PpQq - Two pairs that are heterozygous
6. SSrr - Two pairs that are heterozygous
7. GG - Homozygous
8. LLll - Two pairs that are heterozygous
9. CCrr - Two pairs that are heterozygous
10. Jj - Heterozygous
Understanding Inheritance
The document discusses the concepts of inheritance, genes, alleles, genotypes, phenotypes, and patterns of inheritance. It explains that chromosomes contain genes which control traits, and that offspring inherit genes from both parents. Genotypes are an organism's combination of alleles, while phenotypes are the observable traits. Dominant and recessive alleles can interact in different inheritance patterns like incomplete dominance, codominance, multiple alleles, and polygenic inheritance. An organism's environment and multiple genes can also influence phenotypes. Some disorders are caused by recessive or sex-linked genes.
Patterns of Inheritance
This document discusses patterns of inheritance and genetics terminology. It defines key terms like allele, genotype, phenotype, dominant and recessive traits. It explains Mendel's laws of segregation and independent assortment. It provides examples of monohybrid and dihybrid crosses using Punnett squares. It also discusses exceptions to Mendel's laws like incomplete dominance and codominance. Finally, it covers sex-linked inheritance and examples of X-linked disorders.
Non mendelian inheritance
This document discusses several non-Mendelian inheritance patterns including incomplete dominance, co-dominance, multiple alleles, cytoplasmic inheritance, and genomic imprinting. It provides examples like red and white snapdragon crosses that produce pink flowers to illustrate intermediate inheritance. Dosage compensation and genomic imprinting modify nuclear genes or chromosomes during early development.
7. Patterns of Inheritance
This document provides an outline for a lecture on patterns of inheritance. It covers the topics of genetics and human genetics, Mendel's laws of inheritance, Mendelian traits in humans, and monogenous diseases. The objectives are for students to understand general genetics concepts, key genetic terms, patterns of inheritance, Mendel's laws, and how they apply to inherited human traits and diseases. Example monogenetic diseases and Mendelian traits in humans are also listed.
Heredity and traits
The document discusses heredity and traits. It explains that heredity is the passing of traits from parents to children through genes. Traits are physical or behavioral characteristics that are inherited. Examples given include eye color, hair color, handedness. The document provides several links to websites that further explain heredity and how traits are passed down from generation to generation through chromosomes from each parent combining to form the child's DNA.
Mendel law
Gregor Mendel conducted experiments with pea plants to establish the basic laws of inheritance. He found that traits from parents separate and recombine in predictable ways when passed to offspring. Mendel determined that traits are determined by discrete factors, now known as genes, which are inherited independently of each other. His work established the fundamental rules of genetics and heredity.
Genetics dentistry inheritance patterns or modes of inheritance
This document discusses different patterns of inheritance for genetic traits and disorders, including autosomal dominant, autosomal recessive, and sex-linked inheritance. It provides examples of pedigrees that illustrate each pattern of inheritance and describes key characteristics such as whether a trait is expressed in the heterozygous or homozygous state, risks of inheriting a trait, and the frequency of traits being passed down through generations. The document also discusses concepts like pseudodominance, locus heterogeneity, and how pedigree analysis is used to determine a trait's mode of inheritance.
Genetics
Gregor Mendel studied traits in garden peas and established the principles of heredity through quantitative experiments. He found that traits like seed shape, color, and flower position were inherited based on dominant and recessive alleles. Mendel's work laid the foundation for genetics and showed that heritable traits are passed from parents to offspring via discrete units now known as genes. Genetics further studies how heredity works, including patterns of inheritance, mutations, chromosomal abnormalities, and genetic testing techniques like amniocentesis.
Chpt. 11.2 complex inheritance leftovers
Sickle-cell anemia is an autosomal recessive trait common in those with African and Mediterranean ancestry. It causes abnormally shaped red blood cells, impaired blood flow, tissue damage, and health issues. Sex is determined by the 23rd pair of chromosomes - females have XX and males have XY. The X chromosome carries many genes needed for development in both sexes. To compensate for having two X chromosomes, females inactivate one randomly. Sex-linked traits are on the X chromosome and are always expressed if recessive in females. Muscular dystrophy is an X-linked recessive disease. Polygenic traits like skin and eye color are influenced by two or more genes and result in a range of intermediate phenotypes.
Modes of inheritance
This document discusses different modes of inheritance for genetic diseases. It covers single gene disorders like sickle cell anemia and chromosomal disorders like Down syndrome. It explains Mendel's laws of inheritance including segregation and independent assortment. The major patterns of inheritance are autosomal dominant, autosomal recessive, X-linked dominant, X-linked recessive and mitochondrial. Characteristics of each pattern are provided along with examples. Multifactorial inheritance involving multiple gene loci is also described. The role of genetics and lifestyle in disease development is highlighted.
Non-Mendellian genetics
This document discusses several non-Mendelian patterns of inheritance including lack of dominance where the heterozygous phenotype differs from the homozygous phenotypes, multiple alleles where a single gene can have more than two alleles, pleiotropy where a single gene influences multiple traits, lethal genes which cause death, sex-linked inheritance determined by genes on sex chromosomes, gene interactions between two or more genes, complementary genes which act together to determine a trait, epistasis where one gene inhibits another, polygenic inheritance where multiple genes influence a trait, and pedigree analysis to trace traits within a family.
Lab 6 inheritance of traits fall 2014
This document provides information about genetics and inheritance for a dragon genetics lab. It defines key terms like heredity, traits, alleles, and dominant and recessive genes. It summarizes Gregor Mendel's pioneering work in genetics, including his laws of segregation and independent assortment. The document discusses inheritance patterns for autosomal and sex-linked genes, as well as complex inheritance like incomplete dominance and environmental influences. The goal is for students to understand basic genetics concepts and how they are demonstrated in a model organism.
1. In a given plant, the yellow seed color allele (Y) is dominant to .pdf
1. In a given plant, the yellow seed color allele (Y) is dominant to green seed color (y). Give the
genotypic and phenotypic ratios for the following crosses? a. homozygous yellow x green b.
heterozygous yellow x green c. heterozygous yellow x heterozygous yellow d. green x green 2. If
two animals heterozygous for a single pair of genes are mated and have 276 offspring, how many
would be expected to have the dominant genotype? 3. Two long-winged fies are mated. The
offspring included 90 with long wings and 32 with short wings. Which phenotype is recessive?
4. A blood test reveals that a couple both have the sickle-cell trat. What is the probability of their
producing a child with sickle-cell anemia? 5. A blood type A woman has a type B child. She
accuses a type O man of being the father. Knowing genetics you are asked to give an opinion; do
so. 6. Assume that human eye color is controlled by a single pair of alleles. A blue-eyed man,
both of whose parents were bom brown-eyed, marries a brown-eyed woman whose father was
blue-eyed and whose mother was brown-eyed. They have a blue-eyed child. Which are the
genotypes of all individuals mentioned? 7. A red fruit, tall tomato plant RrTt, is crossed with a
yellow-fruited dwarf plant ritt. What genotypes and phenotypes would be expected in the
offispring? 8. What genotype and phenotype would be expected in the offspring if the cross in
the previous problem had been RrTt x RrTt ?.
Mendelian Genetics.pptx
This document discusses Gregor Mendel and the principles of inheritance through Mendelian genetics. It covers key terms like genotype, phenotype, alleles, dominant/recessive genes, and Mendel's laws of inheritance including segregation, independent assortment, and complete dominance. It provides examples of inheritance patterns in traits like eye color, hair color, plant height and flower color. It also presents genetics problems involving setting up punnett squares and determining genotype and phenotype ratios in offspring.
Genetics-and-Heredity-Intro-
Genetics is the science of heredity, or how traits are passed from parents to offspring. Traits are determined by genes located on chromosomes. Gregor Mendel's experiments with pea plants in the 1800s laid the foundations for genetics by demonstrating that traits are inherited in predictable patterns depending on whether genes are dominant or recessive. The basic principles of inheritance that Mendel discovered include that each parent contributes half of the offspring's genes, and that dominant traits mask recessive traits. Genetic inheritance can be represented using Punnett squares to predict offspring genotypes and phenotypes.
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Pattern of inheritance 01
This document defines key genetic terms and summarizes Mendel's laws of inheritance. It explains that genes determine traits which are passed from parents to offspring. Mendel discovered the laws of dominance, segregation, and independent assortment through his pea plant experiments. The document also outlines different patterns of inheritance such as dominant-recessive, incomplete dominance, co-dominance, sex-linked, and polygenic inheritance. Polygenic traits like skin color are influenced by multiple genes resulting in a continuum of phenotypes.
Human genetics
This document discusses basic concepts in human genetics including genes, chromosomes, DNA, alleles, dominant and recessive traits, and genetic disorders. It covers key topics like the human genome, inheritance from parents, genetic testing methods like amniocentesis and chorionic villus sampling, influences on prenatal development, and genetic counseling.
10. patterns of inheritance
Gregor Mendel's pea plant experiments in the mid-19th century laid the groundwork for genetics by demonstrating that traits are passed from parents to offspring via discrete units of inheritance called genes. The document defines genetic terminology like alleles, genotypes, phenotypes, dominant/recessive traits, and describes Mendel's laws of segregation and independent assortment. It also discusses sex-linked inheritance and variations like incomplete dominance and polygenic traits. Common human genetic disorders are reviewed including examples like sickle cell disease, cystic fibrosis, and Duchenne muscular dystrophy.
1. Genetics and heredity
Genetics is the study of genes, heredity, and variation in living organisms. Genes hold the information to build and maintain an organism. Genes are found within each cell of the body, located on structures called chromosomes within the nucleus. Humans have 23 pairs of chromosomes, with one set inherited from each parent, containing the genes that determine traits like eye color. Differences in genes between individuals result in biological diversity.
Heredity and genetics
Heredity is the passing on of characteristics from one generation to the next. It is the reason why offspring look like their parents. It also explains why cats always give birth to kittens and never puppies. The process of heredity occurs among all living things including animals, plants, bacteria, protists and fungi. The study of heredity is called genetics and scientists that study heredity are called geneticists.
Through heredity, living things inherit traits from their parents. Traits are physical characteristics. You resemble your parents because you inherited your hair and skin color, nose shape, height, and other traits from them.
Cells are the basic unit of structure and function of all living things. Tiny biochemical structures inside each cell called genes carry traits from one generation to the next. Genes are made of a chemical called DNA (deoxyribonucleic acid). Genes are strung together to form long chains of DNA in structures known as chromosomes. Genes are like blueprints for building a house, except that they carry the plans for building cells, tissues, organs, and bodies. They have the instructions for making the thousands of chemical building blocks in the body. These building blocks are called proteins. Proteins are made of smaller units called amino acids. Differences in genes cause the building of different amino acids and proteins. These differences cause individuals to have different traits such as hair color or blood types.
A gene gives only the potential for the development of a trait. How this potential is achieved depends partly on the interaction of the gene with other genes. But it also depends partly on the environment. For example, a person may have a genetic tendency toward being overweight. But the person's actual weight will depend on such environmental factors as how what kinds of food the person eats and how much exercise that person does.
Genetics and inheritance
This document provides an overview of genetics and inheritance concepts taught in Campbell & Reece's chapters 14 and 15. It summarizes Mendel's experiments with pea plants which established the basic principles of heredity, including dominant and recessive traits, genotypes and phenotypes, monohybrid and dihybrid crosses. It also covers sex determination, sex-linked inheritance, degrees of dominance, and polygenic inheritance. Mendel's work laid the foundation for genetics as a scientific field.
Classical genetics
Here are the answers to the seatwork:
1. AA - Homozygous
2. Rr - Heterozygous
3. aaBB - Two pairs that are homozygous
4. MmNN - Two pairs that are heterozygous
5. PpQq - Two pairs that are heterozygous
6. SSrr - Two pairs that are heterozygous
7. GG - Homozygous
8. LLll - Two pairs that are heterozygous
9. CCrr - Two pairs that are heterozygous
10. Jj - Heterozygous
Understanding Inheritance
The document discusses the concepts of inheritance, genes, alleles, genotypes, phenotypes, and patterns of inheritance. It explains that chromosomes contain genes which control traits, and that offspring inherit genes from both parents. Genotypes are an organism's combination of alleles, while phenotypes are the observable traits. Dominant and recessive alleles can interact in different inheritance patterns like incomplete dominance, codominance, multiple alleles, and polygenic inheritance. An organism's environment and multiple genes can also influence phenotypes. Some disorders are caused by recessive or sex-linked genes.
Patterns of Inheritance
This document discusses patterns of inheritance and genetics terminology. It defines key terms like allele, genotype, phenotype, dominant and recessive traits. It explains Mendel's laws of segregation and independent assortment. It provides examples of monohybrid and dihybrid crosses using Punnett squares. It also discusses exceptions to Mendel's laws like incomplete dominance and codominance. Finally, it covers sex-linked inheritance and examples of X-linked disorders.
Non mendelian inheritance
This document discusses several non-Mendelian inheritance patterns including incomplete dominance, co-dominance, multiple alleles, cytoplasmic inheritance, and genomic imprinting. It provides examples like red and white snapdragon crosses that produce pink flowers to illustrate intermediate inheritance. Dosage compensation and genomic imprinting modify nuclear genes or chromosomes during early development.
7. Patterns of Inheritance
This document provides an outline for a lecture on patterns of inheritance. It covers the topics of genetics and human genetics, Mendel's laws of inheritance, Mendelian traits in humans, and monogenous diseases. The objectives are for students to understand general genetics concepts, key genetic terms, patterns of inheritance, Mendel's laws, and how they apply to inherited human traits and diseases. Example monogenetic diseases and Mendelian traits in humans are also listed.
Heredity and traits
The document discusses heredity and traits. It explains that heredity is the passing of traits from parents to children through genes. Traits are physical or behavioral characteristics that are inherited. Examples given include eye color, hair color, handedness. The document provides several links to websites that further explain heredity and how traits are passed down from generation to generation through chromosomes from each parent combining to form the child's DNA.
Mendel law
Gregor Mendel conducted experiments with pea plants to establish the basic laws of inheritance. He found that traits from parents separate and recombine in predictable ways when passed to offspring. Mendel determined that traits are determined by discrete factors, now known as genes, which are inherited independently of each other. His work established the fundamental rules of genetics and heredity.
Genetics dentistry inheritance patterns or modes of inheritance
This document discusses different patterns of inheritance for genetic traits and disorders, including autosomal dominant, autosomal recessive, and sex-linked inheritance. It provides examples of pedigrees that illustrate each pattern of inheritance and describes key characteristics such as whether a trait is expressed in the heterozygous or homozygous state, risks of inheriting a trait, and the frequency of traits being passed down through generations. The document also discusses concepts like pseudodominance, locus heterogeneity, and how pedigree analysis is used to determine a trait's mode of inheritance.
Genetics
Gregor Mendel studied traits in garden peas and established the principles of heredity through quantitative experiments. He found that traits like seed shape, color, and flower position were inherited based on dominant and recessive alleles. Mendel's work laid the foundation for genetics and showed that heritable traits are passed from parents to offspring via discrete units now known as genes. Genetics further studies how heredity works, including patterns of inheritance, mutations, chromosomal abnormalities, and genetic testing techniques like amniocentesis.
Chpt. 11.2 complex inheritance leftovers
Sickle-cell anemia is an autosomal recessive trait common in those with African and Mediterranean ancestry. It causes abnormally shaped red blood cells, impaired blood flow, tissue damage, and health issues. Sex is determined by the 23rd pair of chromosomes - females have XX and males have XY. The X chromosome carries many genes needed for development in both sexes. To compensate for having two X chromosomes, females inactivate one randomly. Sex-linked traits are on the X chromosome and are always expressed if recessive in females. Muscular dystrophy is an X-linked recessive disease. Polygenic traits like skin and eye color are influenced by two or more genes and result in a range of intermediate phenotypes.
Modes of inheritance
This document discusses different modes of inheritance for genetic diseases. It covers single gene disorders like sickle cell anemia and chromosomal disorders like Down syndrome. It explains Mendel's laws of inheritance including segregation and independent assortment. The major patterns of inheritance are autosomal dominant, autosomal recessive, X-linked dominant, X-linked recessive and mitochondrial. Characteristics of each pattern are provided along with examples. Multifactorial inheritance involving multiple gene loci is also described. The role of genetics and lifestyle in disease development is highlighted.
Non-Mendellian genetics
This document discusses several non-Mendelian patterns of inheritance including lack of dominance where the heterozygous phenotype differs from the homozygous phenotypes, multiple alleles where a single gene can have more than two alleles, pleiotropy where a single gene influences multiple traits, lethal genes which cause death, sex-linked inheritance determined by genes on sex chromosomes, gene interactions between two or more genes, complementary genes which act together to determine a trait, epistasis where one gene inhibits another, polygenic inheritance where multiple genes influence a trait, and pedigree analysis to trace traits within a family.
Lab 6 inheritance of traits fall 2014
This document provides information about genetics and inheritance for a dragon genetics lab. It defines key terms like heredity, traits, alleles, and dominant and recessive genes. It summarizes Gregor Mendel's pioneering work in genetics, including his laws of segregation and independent assortment. The document discusses inheritance patterns for autosomal and sex-linked genes, as well as complex inheritance like incomplete dominance and environmental influences. The goal is for students to understand basic genetics concepts and how they are demonstrated in a model organism.
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Genetics dentistry inheritance patterns or modes of inheritance
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Similar to Genetics test review
1. In a given plant, the yellow seed color allele (Y) is dominant to .pdf
1. In a given plant, the yellow seed color allele (Y) is dominant to green seed color (y). Give the
genotypic and phenotypic ratios for the following crosses? a. homozygous yellow x green b.
heterozygous yellow x green c. heterozygous yellow x heterozygous yellow d. green x green 2. If
two animals heterozygous for a single pair of genes are mated and have 276 offspring, how many
would be expected to have the dominant genotype? 3. Two long-winged fies are mated. The
offspring included 90 with long wings and 32 with short wings. Which phenotype is recessive?
4. A blood test reveals that a couple both have the sickle-cell trat. What is the probability of their
producing a child with sickle-cell anemia? 5. A blood type A woman has a type B child. She
accuses a type O man of being the father. Knowing genetics you are asked to give an opinion; do
so. 6. Assume that human eye color is controlled by a single pair of alleles. A blue-eyed man,
both of whose parents were bom brown-eyed, marries a brown-eyed woman whose father was
blue-eyed and whose mother was brown-eyed. They have a blue-eyed child. Which are the
genotypes of all individuals mentioned? 7. A red fruit, tall tomato plant RrTt, is crossed with a
yellow-fruited dwarf plant ritt. What genotypes and phenotypes would be expected in the
offispring? 8. What genotype and phenotype would be expected in the offspring if the cross in
the previous problem had been RrTt x RrTt ?.
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This document discusses Gregor Mendel and the principles of inheritance through Mendelian genetics. It covers key terms like genotype, phenotype, alleles, dominant/recessive genes, and Mendel's laws of inheritance including segregation, independent assortment, and complete dominance. It provides examples of inheritance patterns in traits like eye color, hair color, plant height and flower color. It also presents genetics problems involving setting up punnett squares and determining genotype and phenotype ratios in offspring.
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Genetics is the science of heredity, or how traits are passed from parents to offspring. Traits are determined by genes located on chromosomes. Gregor Mendel's experiments with pea plants in the 1800s laid the foundations for genetics by demonstrating that traits are inherited in predictable patterns depending on whether genes are dominant or recessive. The basic principles of inheritance that Mendel discovered include that each parent contributes half of the offspring's genes, and that dominant traits mask recessive traits. Genetic inheritance can be represented using Punnett squares to predict offspring genotypes and phenotypes.
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This document provides information about genetics and Mendelian inheritance. It begins with an introduction to important figures in the history of genetics like Gregor Mendel. It then discusses the three main theories of inheritance pre-Mendel and the history of genetics including Mendel's experiments and laws of inheritance. The rest of the document details various genetics concepts like linkage, crossing over, aneuploidy and their relationships to chromosomes and inheritance patterns.
Getting into genes slideshare copy
This document provides an overview of DNA and genetics. It contains 3 key points:
1) DNA is the blueprint that controls characteristics of organisms. It is located in the nucleus of cells in the form of chromosomes which contain genes.
2) Humans have 23 pairs of chromosomes, or 46 total chromosomes in each cell. The 23rd pair determines gender - XX for females and XY for males.
3) Experiments can be done to extract and work with DNA, such as from strawberries, to learn more about its structure and role in heredity.
Chapter 3 The New GeneticsAlma Villanueva, MACalifornia S.docx
Chapter 3:
The New Genetics
Alma Villanueva, MA
California State University, Los Angeles
Overview
Genetic Code
The Beginning of Life
Male & Female
Twins
Genotype & Phenotype
Disorders
Genetic Counseling
Genetic Code
Cells
Basic unit of life
Trillions!
Nucleus
Chromosomes
Thread– like structures made up of DNA & protein
23 pairs
DNA (Deoxyribonucleic acid)
2 strands twisted in a double helix
Chemical composition of molecules that contain the genes
Contains all of the information required to build/maintain the cell
3
Genes
Small section of the chromosome
18,000 – 23,000 genes
Each gene provides a unique recipe to make a protein
4 bases
Code for your traits
A - adenine
T - thymine
C - cytosine
G – guanine
Only 4 possible pairs
A-T; T-A; C-G; G-C
http://mybrainnotes.com/brain-dna-behavior.html
4
Allele
A variation of a gene
Example: the gene for eye color has several variations (alleles); an allele for blue eye color or an allele for brown eyes
Everyone inherits alleles from sperm & ovum
Genetic diversity
Distinguishes each person
Allows the human species to adapt to pressures of the environment
Genome
Full set of genes with instructions to make a living organism
Genomes exist for each species
Video about Genes
5
The Beginning of Life
Two Parents, Millions of Gametes
Gamete
Reproductive cell
Sperm or Ovum
Each contains 23 pairs
Zygote
Cell formed with union of Sperm & Ovum
Produce a new individual with 23 chromosomes from each parent
Conception
http://predictingbabygender.info/tag/intercourse-timing/
Matching genes
Genotype
Organism’s entire genetic inheritance, or genetic potential.
Homozygous (same zygote)
Two genes of one pair that are exactly the same in every letter of their code
Heterozygous
Two genes of one pair that differ in some way
Usually not an issue
Male of Female?
Humans usually possess
46 chromosomes
44 autosomes and 2 sex chromosomes
SEX chromosome = 23rd pair
Female – XX
Male – XY
Mother’s contain X
Father’s may have X or Y
X chrom. Is larger & more genes
Y contain SRY,
making male hormones & organs
It's a girl!
Uncertain Sex
“ambiguous genitals,” = child's sex is not abundantly clear
a quick analysis of the chromosomes is needed, to make sure there are exactly 46 and to see whether the 23rd pair is XY or XX
shown here a baby boy (left) and girl (right).
Too Many Boys?
Is sex selection the parents’ right or a social wrong?
Preference for boys in many areas of world
Ways to prevent female birth
Inactivating X sperm before conception
In vitro fertilization (IVF)
Aborting XX fetuses
My Strength, My Daughter
slogan these girls in New Delhi are shouting at a demonstration against abortion of female fetuses in India
The current sex ratio of children in India suggests that this campaign has not convinced every couple.
New Cells
Within hours of conception
23 pairs of chromosomes carrying all the genes duplicate, forming two complete sets of the genome
Two sets.
Chapter 3 The New GeneticsAlma Villanueva, MACalifornia S.docx
Chapter 3:
The New Genetics
Alma Villanueva, MA
California State University, Los Angeles
Overview
Genetic Code
The Beginning of Life
Male & Female
Twins
Genotype & Phenotype
Disorders
Genetic Counseling
Genetic Code
Cells
Basic unit of life
Trillions!
Nucleus
Chromosomes
Thread– like structures made up of DNA & protein
23 pairs
DNA (Deoxyribonucleic acid)
2 strands twisted in a double helix
Chemical composition of molecules that contain the genes
Contains all of the information required to build/maintain the cell
3
Genes
Small section of the chromosome
18,000 – 23,000 genes
Each gene provides a unique recipe to make a protein
4 bases
Code for your traits
A - adenine
T - thymine
C - cytosine
G – guanine
Only 4 possible pairs
A-T; T-A; C-G; G-C
http://mybrainnotes.com/brain-dna-behavior.html
4
Allele
A variation of a gene
Example: the gene for eye color has several variations (alleles); an allele for blue eye color or an allele for brown eyes
Everyone inherits alleles from sperm & ovum
Genetic diversity
Distinguishes each person
Allows the human species to adapt to pressures of the environment
Genome
Full set of genes with instructions to make a living organism
Genomes exist for each species
Video about Genes
5
The Beginning of Life
Two Parents, Millions of Gametes
Gamete
Reproductive cell
Sperm or Ovum
Each contains 23 pairs
Zygote
Cell formed with union of Sperm & Ovum
Produce a new individual with 23 chromosomes from each parent
Conception
http://predictingbabygender.info/tag/intercourse-timing/
Matching genes
Genotype
Organism’s entire genetic inheritance, or genetic potential.
Homozygous (same zygote)
Two genes of one pair that are exactly the same in every letter of their code
Heterozygous
Two genes of one pair that differ in some way
Usually not an issue
Male of Female?
Humans usually possess
46 chromosomes
44 autosomes and 2 sex chromosomes
SEX chromosome = 23rd pair
Female – XX
Male – XY
Mother’s contain X
Father’s may have X or Y
X chrom. Is larger & more genes
Y contain SRY,
making male hormones & organs
It's a girl!
Uncertain Sex
“ambiguous genitals,” = child's sex is not abundantly clear
a quick analysis of the chromosomes is needed, to make sure there are exactly 46 and to see whether the 23rd pair is XY or XX
shown here a baby boy (left) and girl (right).
Too Many Boys?
Is sex selection the parents’ right or a social wrong?
Preference for boys in many areas of world
Ways to prevent female birth
Inactivating X sperm before conception
In vitro fertilization (IVF)
Aborting XX fetuses
My Strength, My Daughter
slogan these girls in New Delhi are shouting at a demonstration against abortion of female fetuses in India
The current sex ratio of children in India suggests that this campaign has not convinced every couple.
New Cells
Within hours of conception
23 pairs of chromosomes carrying all the genes duplicate, forming two complete sets of the genome
Two sets ...
Unit 4 genetics and inheritance(2)
This document provides an overview of genetics and inheritance concepts including:
- Mendel discovered the basic principles of heredity through pea plant experiments including dominant and recessive traits.
- Genetic crosses can be used to determine the likelihood of offspring inheriting certain traits based on the parents' genotypes.
- Additional concepts covered include independent assortment, polygenic inheritance, sex determination, and sex-linked inheritance.
genetics and inheritance
This document provides an overview of genetics and inheritance concepts including:
- Mendel discovered the basic principles of heredity through pea plant experiments and developed the laws of segregation and independent assortment.
- Genetic crosses can be used to determine the possible outcomes and traits of offspring. Monohybrid and dihybrid crosses examine one or two trait pairs.
- Genes exist in alleles that are dominant or recessive and determine an organism's genotype and phenotype. Sex is determined by X and Y chromosomes.
Geneticsand heredity
Gregor Mendel was an Austrian monk who is considered the father of genetics. In the mid-1800s, he conducted experiments breeding pea plants and discovered the basic principles of heredity. He found that traits are passed from parents to offspring through discrete factors that we now call genes. Mendel's work laid the foundation for modern genetics and showed that inheritance follows specific biological rules.
Dr. hajare balaji b [genetics}
introduction of genetics by DR. Hajare Balaji
genetic basis of inheritance
moleculae basis of inheritance
chromosomal basis of inheritance
Human Inheritance & Genetic Disorders
This document discusses human genetics and genetic disorders. It explains that genes located on chromosomes control human traits and can cause disorders if mutated or in an abnormal number. Some examples of genetic disorders mentioned are cystic fibrosis caused by a recessive gene mutation, sickle cell anemia caused by a codominant allele, and Down syndrome caused by an extra 21st chromosome. Pedigrees and karyotypes are tools that can be used to study genetics and identify genetic disorders in families.
Chapter 14: Mendel and Genes
KEY CONCEPTS
14.1 Mendel used the scientific approach to identify two laws of inheritance
14.2 Probability laws govern Mendelian inheritance
14.3 Inheritance patterns are often more complex than predicted by simple Mendelian genetics
14.4 Many human traits follow Mendelian patterns of
inheritance
Chapter14genes 151125145851-lva1-app6891
Mendel's laws of segregation and independent assortment govern inheritance. When crossing two heterozygotes with different alleles at the same locus, DaDb and DcDd, the alleles will segregate and assort independently. This results in offspring genotypes in a 1:2:1:2:1:2:1:1 ratio.
Chapter14genes 151125145851-lva1-app6891
Mendel's laws of segregation and independent assortment govern inheritance patterns. When Mendel crossed two heterozygotes with different alleles at the same locus (DaDb x DcDd), he would expect the following genotype proportions in the offspring:
1) 9% DaDa, DbDb, DcDc, DdDd (homozygotes)
2) 24% DaDb, DaDc, DaDd, DbDc, DbDd, DcDd (heterozygotes)
3) 43% DaDc, DaDd, DbDc, DbDd (other heterozygotes)
The alleles assort independently during gamete formation, allowing for all possible combinations in a 9:
Genetics review sheet
This document provides a genetics review with 12 questions covering key topics in Mendelian and non-Mendelian genetics. It asks students to define important genetic terms like gene and allele. It also asks students to solve Punnett squares involving traits like tongue rolling, nose and ear size in trolls, and flower color in roses. The review covers non-Mendelian inheritance patterns like incomplete dominance and codominance. It also addresses sex-linked traits and asks students to solve genetics problems involving traits like colorblindness. Finally, it provides pedigree problems for students to analyze inheritance patterns.
DNA Genes and Chromosomes.pptx
Here are definitions for the requested concepts:
A. Sex linked traits: Traits that are determined by genes located on the X or Y chromosomes. Examples include color blindness and hemophilia.
B. Sex limited traits: Traits that are expressed in one sex but not the other. Examples include lactation in females and beard growth in males.
C. Sex influenced traits: Traits whose expression depends on the sex of the individual, but can be expressed in both sexes. Examples include height and athletic ability which tend to be more pronounced in one sex.
Similar to Genetics test review (20)
1. In a given plant, the yellow seed color allele (Y) is dominant to .pdf
1. In a given plant, the yellow seed color allele (Y) is dominant to .pdf
Chapter 3 The New GeneticsAlma Villanueva, MACalifornia S.docx
Chapter 3 The New GeneticsAlma Villanueva, MACalifornia S.docx
Chapter 3 The New GeneticsAlma Villanueva, MACalifornia S.docx
Chapter 3 The New GeneticsAlma Villanueva, MACalifornia S.docx
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Transcription notes
Protein is made from amino acids that interact through bonding and folding. Proteins control traits like hair and skin color through the amount of melanin present. Blood carries oxygen using the protein hemoglobin. DNA contains genes and remains in the nucleus, while messenger RNA (mRNA) acts as an intermediary, traveling between the nucleus and cytoplasm to create proteins. Transcription involves DNA unzipping and mRNA being built from the DNA template. Translation occurs when mRNA leaves the nucleus and attaches to ribosomes to recruit transfer RNA (tRNA) and amino acids to build a protein chain.
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