Chapter 27 Human Genetics. Karyotype The arrangement of all the chromosomes found in a cell. Includes: 23 rd pair Female sex chromosomes X X Female =

Slides:



Advertisements
Similar presentations
Human Heredity.
Advertisements

Human Heredity.
Complex Inheritance of Human Traits
Genetic Mutations & Pedigrees
Patterns of Heredity and Human Genetics
Chromosomes and Inheritance
#4- skip HW # 68- Practice with Punnett Squares – worksheet Warm up
Chapter 12 Section 3-Complex Inheritance of Human Traits.
Patterns of Heredity and Human Genetics
Karyotypes and Sex-Linked Traits
Genetics Chapter 29. Essential Must Know Terminology Chromosome Homologous (homologs) chromosomes – Autosomes – Sex chromosomes – Karyotype Gene Alleles.
Genetics Chapter 29. Essential Must Know Terminology Chromosome: structure of DNA seen in cell division – Homologous chromosomes Autosomes: 22 homologs.
Continuing Genetics DOMINANCE Unit 5: Mendelian Genetics
Chapter 12: Patterns of Heredity & Human Genetics
Standard Biology Chapter 27 Human Genetics
Chapter 11 Human Heredity.
Chapter 12 PATTERNS OF HEREDITY AND HUMAN GENETICS.
Chapter 12.  Humans have 46 chromosomes  44 are autosomes  22 pairs of homologous chromosomes  2 are sex chromosomes: X and Y  Females have two X.
Making a Pedigree Pedigree – a graphic representation of genetic inheritance Geneticists often need to map the inheritance of genetic traits from generation.
Human Heredity Who and What and Why of Humans? New Flash…….. It has been discovered that having a glowing “red nose” is a recessive sex-linked trait.
Human Genetics Chapter 12.
Tracing the Inheritance of the Human Y Chromosome
Unit 4--Genetics Chapter 14 Human Heredity. 1) Autosomes –all the chromosomes except the sex chromosomes (in humans, there are 22 pair) 2) Sex chromosomes.
Complex Inheritance and Human Heredity Chapter 11.
Human Inheritance Chapter 14 sec. 1 and 2. Pedigree Analysis Pedigree = a family record that shows how a trait is inherited over several generations.
Human Genetics Chapter 7 1. The Role of Chromosomes A. Chromosome number 1.Each human sperm/egg has 23 chromosomes 2.Each human body cell has 23 pairs.
Variations to Inheritance Exceptions to Mendel’s Laws.
Two copies of each autosomal gene affect phenotype (physical). Mendel studied autosomal gene traits, like hair texture. Autosome – chromosome with genes.
Other Types of Inheritance Epistasis – one gene affects the expression of another gene – Example: albinism – gene for color and a gene for how MUCH color.
Ch.11 – Complex Inheritance & Human Heredity 11.2 – Complex Patterns of Inheritance Sometimes inheritance does not follow Mendel’s rules (Non-Mendelian.
Chromosomes and Human Inheritance - Patterns of Inheritance.
Applied Biology Genetics Notes. Genetics Introduction Genetics is the study of heredity Heredity explains why you look like your parents or siblings (similar.
Pedigree definition  Pedigree: a family history that shows how a trait is inherited over several generations  Pedigrees are usually used when parents.
Unit 7: Complex Inheritance Click to begin Which of the following genotypes represents Type O blood? A.) I A I A B.) I A i C.) I A I B D.) ii L D.)
MORE GENETICS VOCABULARY & EXAMPLES
COMPLEX INHERITANCE OF HUMAN TRAITS
Complex Inheritance Patterns. 1.Incomplete Dominance – phenotype of heterozygous is intermediate of the 2 homozygous phenotypes -results in the blending.
WARM UP # 1/31 Unscramble the words from this chapter Bonus – 1 st 3 people who show me get EC slips! 1. D M E N L E 2. L A L E L 3. M E H C O S R O O.
AP Biology Beyond Mendel’s Laws of Inheritance.
REVIEW GENETICS- the study of heredity. Inheritance Traits are specific characteristics inherited from parents Genes are the factors that determine traits.
What determines are phenotypes? Autosomes- chromosomes 1-44, pairs 1-22 Sex chromosomes- 23 rd pair of chromosomes – Females have two copies of a large.
Chromosomes and Human Inheritance
Chapter 14 – Human Genome.
Complex Patterns of Inheritance
Chapter 14 Human Genetics Human Chromosomes Genome = the full set of genetic information that an organism carries in its DNA Karyotype = the complete.
Human Genetic Disorders Every cell in the human body has 46 chromosomes except for gametes, egg sperm cells, which contain 23 or the haploid number. Human.
27.2 Human Traits Survey Complete Dominance Incomplete Dominance X-Linked Traits.
Human Genetics Inheritance in humans Male/female Multiple Alleles Inherited diseases Twins Sex-linked traits.
Chapter 12 When Heredity Rules are Different. Complex Patterns of Heredity Most traits are not simply dominant or recessive Incomplete dominance: when.
Chapter 4 Part 2- Genetics Since Mendel Life Science.
Two copies of each autosomal gene affect phenotype (physical). Mendel studied autosomal gene traits, like hair texture. Autosome – chromosome with genes.
Chapter 14 Human Heredity. Human Chromosomes A picture of chromosomes arranged in this way (previous page) is know as a karyotype. This karyotype is.
Genetic Diseases & Disorders Biology Genetics Diseases outline Dominant 1. Huntington’s Recessive 1. Cystic fibrosis 2. Sickle-cell anemia 3. Tay-Sachs.
Sex-Linked Traits. Inheritance of Traits  X-linked Disorders - occur mainly in males because the mother usually donates the recessive allele and males.
Complex Patterns of Inheritance. 1.Incomplete dominance 2.Codominance 3.Multiple alleles 4.Sex linked inheritance 5.Polygenic inheritance.
HUMAN GENETICS Pedigree A graphic representation of genetic inheritance. Looks like a family tree.
Genetics Notes Who is Gregor Mendel? Principle of _____________________– Inheritance of one trait has _________________on the inheritance of another trait.
Chapter 12 Patterns of Heredity And Human Genetics.
More Patterns of Inheritance Autosomal inheritance – genes are located on the autosomes, same for both male and female Sex-linked inheritance – genes located.
BIO.7 - GENETICS NON-MENDELIAN GENETICS. Incomplete Dominance In Heterozygous genotypes a COMBINATION of alleles are expressed (somewhere in the middle)
1 Chapter 12 College Prep Biology Patterns of Heredity & Human Genetics.
Patterns of Inheritance
Human Heredity and Genetic Disorders
Genetics Notes Who is Gregor Mendel? “Father of Genetics”
Extensions on Mendelian Genetics
Mendelian Inheritance of Human Traits
Chapter 12.2-When Heredity Follows Different Rules
Patterns of Heredity & Human Genetics
(Where did you get your genes?)
Chapter 5 Notes Heredity.
Presentation transcript:

Chapter 27 Human Genetics

Karyotype The arrangement of all the chromosomes found in a cell. Includes: 23 rd pair Female sex chromosomes X X Female = Male = Sex Chromosomes: chromosome pair 23 Autosomes: chromosome pairs 1-22 X X Y

FEMALE MALE Sex Chromosomes (they determine male or female) “Autosomes”

Amniocentesis A medical technique used to collect the chromosomes of a developing fetus. It is done by inserting a needle into the womb and gathering cells in the amniotic fluid.

Problems that may show up in a karyotype… 1. Turner’s syndrome: female missing an X chromosome…only 45 total chromosomes Underdeveloped female sex characteristics short stocky stature, underdeveloped breasts, late developer, possibly sterile. NO mental retardation May be aided by hormones Missing chromosome #23

2. Klinefelter’s Syndrome: Male with extra X on the 23 rd pair (sex chromosomes XXY) Symptoms may include more feminine characteristics such as high voice, lack of facial hair, breast development. Mental retardation is usually associated with Klinefelters. Extra X chromosome

3. Down Syndrome iosis%20I.htm Autosomal disorder found on the 21 st chromosome, and therefore can be male or female Extra chromosome #21….also called Trisomy 21. Symptoms include, overlapping skin at the eyes, round shaped head, straight thin hair, short and stocky, and may be sterile. Mental retardation is associated with Down Syndrome.

Statistics… Age of Mother Frequency of Down Syndrome Frequency of Any Chromosomal Disorder in in in in in in in in in in 82 1 in 63 1 in 49 1 in 38 1 in 30 1 in in in in in in in in 83 1 in 66 1 in 53 1 in 42 1 in 33 1 in 26 1 in 21

1. Color blindness genetic disorder found on the sex chromosome X known as a “sex-linked” because its found on chromosome 23 Sex-linked disorders found on the chromosomes… Sex 23 rd pair

XCXC XCXC XCXC Y XCXC XCXC XCXC XCXC XCXC XCXC YY Color blind Dad and Normal mother produces…. XCXC XCXC XCXC Y XCXC XCXC XCXC XCXC XCXC XCXC YY Normal Dad and Carrier mother produces…. What is the only way to get a color-blind daughter?? Two normal sons 2 “carrier” daughters (NOT color blind) 1 color blind son, 1 normal son 1 “carrier” daughter, 1 normal daughter

Color-blind people have trouble distinguishing certain colors (ex: red/green) They DO NOT just “see everything in black and white!!” Misconception:

2.Hemophilia Blood disorder found on the X chromosome (sex-linked) Blood does not clot correctly Known as the “royal genetic disorder” because it’s history is traced back to the European royal families. This is a _________________ showing the actual genetic inheritance of hemophilia in the European royal families… Compare the number of females that suffered to the number of males!! Females: _______ Males: _______ pedigree 0 10

1. Blood Type there are _________________________ 4 different blood types Blood TypeGenes Blood Type AA A or A O Blood Type BB B or B O Blood Type ABA B Blood Type OO

Which blood types are compatible for transfusion?? OB Yes or No ? BA AA B A O Yes No Yes

AA B B AO B O AB A B AB O O OO A O AO A O AB BO AOOO AAAB BB AO BO OO AA

Blood type statistics… If there are 100 people in the room: 39 will be O+ 7 will be O- 34 will be A+ 6 will be A- 9 will be B+ 2 will be B- 3 will be AB+ and only 1 in 200 will be AB- Note: The + and – is the presence (or absence) of a third antigen (Rh).

Sickle-cell anemia blood disorder where the blood cells are sickle-shaped rather than round. The disorder is found on chromosome 11 and is therefore not sex-linked. The Oxygen carrying hemoglobin can not carry oxygen as efficiently and the odd-shaped cells can easily clot and break. Fatigue, pain, and organ failure due to lack of oxygen supply are common symptoms of sickle cell anemia. It is common in the African community Normal RBCSickle-cell

R = round blood cell R’ = sickle cell R R’ = carrier RR R’ R R R R Actual blood cells R’ R R R’

Incomplete dominance Red White X Pink. There is a third color that exists in the heterozygous type. It’s a mixture between the two homozygous types.

Co-Dominance PINKWHITE PINK AND WHITE

Polygenic traits Many human traits are influenced by MORE than one gene!!