Is the mother color blind?

Slides:



Advertisements
Similar presentations
1. The gene for tall plants (T) is dominant over the gene for dwarf or short plants (t) in peas. A homozygous tall plant is crossed with a heterozygous.
Advertisements

Practice Genetics Problems Oh, boy!. Problem #1 In pea plants, the allele for green pods (G) is dominant and the allele for yellow pods (g) is recessive.
7.4 Human Genetics and Pedigrees
Genetics: Complex Inheritance, Sex Linkage, X-Inactivation
Investigating different patterns of inheritance
Genetics.
A Plethora of Punnett Squares!
AUTOSOMES= The first 22 pairs of homologous chromosomes. All of the chromosomes surrounded by the red box are autosomes or autosomal chromosomes.
Sex-linked traits. Sex chromosomes carry genes that code for traits other than gender. Traits determined by genes on the X chromosome are called sex-linked.
Sex-Linked Genes Ms. Klinkhachorn March 21, 2011 Biology.
1. A nonhemophiliac man marries a nonhemophiliac woman whose father was a hemophiliac. What kinds of children can they have and in what percentages?
Not that kind of jeans! A second pair of genes! Oh meiosis!Dominant? Or maybe not What will they inherit?
A man with a Widow’s Peak and a woman with a Widow’s peak have only children who have Widow’s peaks. In another case, two people with Widow’s peaks have.
What information can be revealed by a Punnett square. A
Monogenic disorders risk calculations seminar No 425 Heredity.
Tay-Sachs is a metabolic disorder that results in deterioration of the brain and nervous system, causing an early death in children (usually by age 5).
Genetics Game Autosomal Recessive Inheritance
Sex Determination People – 46 chromosomes or 23 pairs 22 pairs are homologous (look alike) – called autosomes – determine body traits 1 pair is the sex.
Do Now Answer the questions below in your notebook/binder:
What is the gender of the person on the left? What are pedigrees used to show? KSUCommencementTickets.com.
Genetics: Complex Inheritance, Sex Linkage, X-Inactivation AP Biology Unit 3.
Anna and Kristoff are heterozygous for three traits (PTC taster, dimples and freckles). What is the chance of: 1. Their child having the same characteristics.
Pedigrees & More Genetics
Pedigrees Pedigrees study how a trait is passed from one generation to the next. Infers genotypes of family members Disorders can be carried on… – Autosomes.
Sex-Linked Punnett Square Notes
Genetics Quick Review of Grade 11 Sex Linked Traits
SEX-LINKED TRAITS Solving pedigrees for traits with genes located on the X and Y chromosome.
Mendel studied autosomal gene traits The “either-or” traits that were seen in your tutorial. Genes found on autosomes (1-22 for humans) = autosomal.
Sex-Linked Inheritance
Through a family tree, you can identify the relationships among your cousins, aunts, uncles, grandparents, and great-grandparents. Something to remember.
A man and a woman marry. The man is colorblind, which is an X-linked disease. They have 4 children, 2 carrier daughters , 1 completely healthy boy and.
Sex-Linked Inheritance.  Genetically, what determines whether a fetus is a boy or girl?  Who determines gender, Mom or Dad? Explain.
CAN YOU SEE ALL THE PRETTY COLORS?? Are females genetically superior to males? Let’s find out!!
Genetics Problems. Dominant/Recessive Type A Black fly is crossed with a gray fly to produce offspring of which 1/2 are black and 1/2 are gray. What are.
DO NOW WRITE THE DEFINTION FOR EACH OF THE FOLLOWING USE YOUR NOTES!!!
Human Heredity.
SEX-LINKED INHERITANCE X Marks the Spot!. Sex Chromosomes Humans normally possess 23 pairs of chromosomes. – 22 of these pairs are identical in both genders.
Scheda 4. SEX LINKAGE. Human Male Karyotype Human Female Karyotype X-LINKED inheritance: If the trait is recessive and associated with X chromosome, the.
Color blindness is a recessive genetic disorder that is carried on the X chromosome. Answer the following questions about the family of a baby boy who.
No Bell Work today! Set up the next page in your journal… Page: 46 Date: Title: Genetics – Sex-linked Essential Question: How can I predict genetic.
Special Crosses II: Blood and Sex-Linked What are multiple alleles? Multiple Alleles: when two or more alleles contribute to the phenotype. Example-
Sex Determination In humans, the X and Y chromosomes control the sex of offspring. Outcome is always 50% chance of a male, and 50% chance of a female Female.
Chapter 5:1 Human Inheritance. Different traits are determined by a variety of inheritance patterns Single Genes with two alleles Single Genes with two.
Sex-Linked Traits. Inheritance of Traits  X-linked Disorders - occur mainly in males because the mother usually donates the recessive allele and males.
For all the problems in this PPT you must give GENOTYPE and PHENOTYPE percentages/fractions. You also must answer whatever question is asked by the problem.
Genetics Review.
Scheda 4. SEX LINKAGE.
Jeopardy!! Our topic: Genetics!.
Non-Mendelian: Sex- Linked Traits
Sex-Linked Punnett Square Notes
SEX-LINKED GENES.
SEX-LINKED GENES.
Welcome to Jeopardy! Today’s Topic: Genetics
Non-Mendelian: Sex- Linked Traits
Extensions on Mendelian Genetics
Sex Linked Inheritance
GENETICS.
Sex-Linked Inheritance.
Sex-Linked Inheritance.
Non-Mendelian: Sex- Linked Traits
Sex Linked Traits Males vs. Females.
PEDIGREES.
Sex-linked Inheritance
Scheda 4. SEX LINKAGE.
Sex-Linked Traits.
Sex-Linked Traits.
The deadline for all missing assignments is Friday, March 8 at 3:30.
Is the mother color blind?
Genetic Blood Disorders
Presentation transcript:

Is the mother color blind? Color blindness is a recessive genetic disorder that is carried on the X chromosome. Answer the following questions about the family of a baby boy who was born with this disorder. Is the mother color blind? You don’t know, but probably not. Is the father color blind? You don’t know, but probably not. If he is, it’s a coincidence. Did the boy get the disorder from his mom or his dad? Mom

Vitamin D-resistant rickets is a dominant genetic disease that is carried on the X chromosome. Answer the following questions about the family of a baby boy who was born with this disease Does the mother have D- resistant rickets? Yes  Does the father have D-resistant rickets? It’s very unlikely. If he does, it’s a coincidence. Did the boy get the disease from his mom or his dad? Mom 

XBX b x XbY 1/4 Xb Y Xb Xb Xb Y XB XB Xb XB Y A woman is heterozygous for colorblindness and her husband is colorblind. What is the probability that their first child will be a colorblind girl? XBX b x XbY 1/4 Xb Y Xb Xb Xb Y XB XB Xb XB Y

CLS is caused by a X-linked dominant allele CLS is caused by a X-linked dominant allele. A normal woman and a man with CLS have a daughter. What are the chances that the girl has CLS? 100% CLS is characterized by severe mental problems and is sometimes associated with growth abnormalities. You won’t need to remember this for a test..

ALD is caused by a X-linked recessive allele ALD is caused by a X-linked recessive allele. A normal woman (whose father had ALD) marries a man with ALD. What fraction of their children are expected to be girls with ALD?. 25% Xa Y Xa Xa Xa Y XA XA Xa XA Y

A man with a widow’s peak (an autosomal dominant allele) and normal color vision marries a color-blind woman with a straight hairline. The man’s father had a straight hairline, as did both of the woman’s parents. What are the genotypes of the couple? Woman: XbXbww Man: XBYWw

Wife: XbXbww Husband: XBYWw If the couple has a child, what are the chances that it will be a son with a widow’s peak? Chance of son: ½ Chance of widow’s peak: ½ Chance the kid with both be a son and have a widow’s peak: (1/2)(1/2) = 1/4

Wife: XbXbww Husband: XBYWw What is that chance that any son the couple has will be colorblind with a straight hairline? Chance that the son will be colorblind: 1 Chance of straight hairline: 1/2 Chance the son will be colorblind and have a straight hairline: (1)(1/2) = 1/2

Wife: XbXbww Husband: XBYWw What is that chance that any daughter the couple has will be colorblind with a widow’s peak? Chance of colorblind daughter: 0 Chance of widow’s peak: ½ Chance of colorblind and widow's peak: (0)(1/2) = 0

Wife: XbXbww Husband: XBYWw Suppose the couple had a daughter with normal color vision and a widow’s peak. What is the chance that she is heterozygous for both conditions? Chance of daughter being heterozygous for colorblindness: 1 Chance of being heterozygous for widow’s peak: 1 Chance of being heterozygous for colorblindness and widow's peak: (1)(1) = 1