Pedigree Analysis Directions: Identify the mode of inheritance as X-linked recessive, X-linked dominant or Y-linked. Explain your answer on your answer sheet. Activity: Activate Wdo
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- Directions: Tell whether the following carry or show the sex-linked recessive spongy-tiny pores trait. Also, tell whether the individuals are male or female. Remember that since most sex-linked traits are recessive, the person who shows the trait can have no X’s with big superscripted letters. So, if a male carries the trait, he must also show the trait.Answer the Guide Questions: What chromosomes will result to a normal phenotype (normal spongy pore trait)? ________________________________________________________________________ Do all individuals who have the spongy tiny pore allele show it in their physical appearance? Why or why not? ________________________________________________________________________ Can males be a carrier of an X-linked recessive trait? How about females? Explain. ________________________________________________________________________ What will be the sex of an individual who is easily affected by an X-linked recessive trait? Why?…A. Identify the type of inheritance from the given options below. Write only the letters of your answer, i.e. AD for autosomal dominant.Autosomal Dominant Autosomal Recessive X-Linked Recessive Y-Linked B. Give the possible genotype of the AFFECTED individuals. In indicating the genotype of affected individual, specify the generation and number where the individual belongs, i.e. II-3 AA; III-1 aa See attached image.Match the descriptions with the appropriate pedigree. Inheritance of a dominant trait Inheritance of a recessive Inheritance of a Inheritance of a X-linked autosomal trait recessive, sex-linked trait trait Pedigree A Pedigree B Pedigree C
- Please answer all of them, they are all connected. PEDIGREE ANALYSIS and SYMBOLOGY: Examine the pedigree which has X linked Dominant inheritance of disorder. Use letter X* (asterisk denotes disorder) as genotype of the individuals which can be XX, XY, X*X*, X*X and X*Y. a. What is the genotype of IV-6? b. What is the genotype of III-6? c. What is the genotype of II-3? d. What is the genotype of III-8? e. If couple I-1 and I-2 will have a son, what is the probability of having the disorder? f. If couple III-8 and III-9 will have another child, what is the probability of having the disorder? g. Theoretically, if individual IV-3 and individual IV-5 will marry and will have a child, what is the probability of having a child without the X-linked disorder?Please find an Image/Graphic to represent sickle cell disease: Use at least two different images to help the audience understand the cause and/or inheritance pattern of the disorder you chose. Include a brief 1-2 sentence caption below each image that gives a description of the image and explains its relevance to your chosen disorder. The two images should NOT convey the same exact information. Ideas of images to use include: karyotypes, pedigrees, DNA sequences, etc. Please note: the images should be specific to your chosen disorder. The 2 required images must be related to cause and/or inheritance pattern. Images of an individual with the disorder will not count toward your 2 required images as they do not contribute to the audience's understanding of cause and/or inheritance pattern.on Instructions: Before Mendel and his results were fully accepted, there were many theories that were proposed that tried to explain how traits were passed on from one generation to another. In the space provided, list down the important points of each theory. Hippocrates’: Brick and Mortar Theory ______________________________________________________________________ ______________________________________________________________________ ______________________________________________________________________ ______________________________________________________________________ ______________________________________________________________________ ______________________________________________________________________ ______________________________________________________________________ ______________________________________________________________________ ________________________________________________ Aristotle: Hereditary Elements in Blood…
- SUBJECT-GENETICS TOPIC: Inheritance Related to Sex Identify some form of abnormalities wherein it could be due to the presence of gene in: X chromosome only b) Y chromosome only ? Give example/s. Some traits are expressed by both in the male and female humans,but kindly elaborate such traits which are only present in male or in female, give example/s which could be explain under sex-limited and sex-influenced genes.Background Reminders: Dominant allele will express itself in the phenotype even when in combination with a different allele (recessive). Example: PP and Pp (purple flowers) Recessive allele does not express itself in the phenotype when combined with another allele (dominant) Example: pp (white flower) -> expressed only when recessive is by itself Problem 1- Autosomal Dominant: Widow’s peak (hairline) Having widow’s peak is a dominant trait (use W and w to represent alleles) A man who has a widow’s peak has a child with a woman that does not have widow’s peak. Their child does not have widow’s peak. What is the genotype of the father? _______________ B.) A man with widow’s peak (WW) has a child with a woman who does not have a widow’s peak. What is the probability their child will have a widow’s peak? ____________ Fill out this Punnett square: C.) If both parents are heterozygous for widow’s peak (Ww)… What is the probability…the Mode of Inheritance (MOI) exercises. Focus on determining the values in the colored cells. Your solutions should read as prose, not simply computations. I have provided values for two MOIs discussed in the lecture, Autosomal Dominant MOI, and X-linked Recessive where the father is affected and the mother is homozygous unaffected. Sometimes, there is confusion regarding defining the disease allele and wild-type allele for a specific mode of inheritance. In this worksheet, you'll note that the D allele is the disease allele for the Autosomal Dominant mode of inheritance. However, it is also the disease allele for the Sex-Linked Recessive mode of inheritance, where the father is affected. The point is, any letter or symbol can represent a disease allele or wild-type allele as long as you define its meaning. For example, I may use r to be the disease allele in an Autosomal Recessive mode of inheritance, and R to be the wild-type allele, or vice versa, as long as I write something like:…
- SUBJECT: GENETICS Topic: Probability 1. Consider albinism a trait to occur in a human family. If two parents areheterozygous for such trait, the probability of having a normally pigmented child is 3//4 and having an albino child is ¼. What is the probability that 2 will be normal and 1 will be albino?I. Perform the indicated single-gene and two-gene crosses. Show all work. Show all Punnett squares. List the gene or genes involved, list and define all allele symbols, and indicate the genotypes of the individuals you are crossing above the Punnett square. Answer questions that ask for a ratio as a ratio and questions that ask for a percent as a percent. One form of red-green color blindness is an X-linked recessive trait. A heterozygote woman has children with a normal man. What is the percentage chance that they will have a child with color blindness?Explain the sex-linked traits. (S9LT-ld-29.4.4) Solve problems related to sex-linked traits. (S9LT-ld-29.4.4) WHAT I NEED (MATERIALS) • Worksheet • Pens WHAT TO DO (PROCEDURE) PART A Directions: Tell whether the following carry or show the sex-linke recessive spongy-tiny pores trait. Also, tell whether the individuals a male or female. Remember that since most sex-linked traits are recessive, the person w shows the trait can have no X's with big superscripted letters. So, if a m carries the trait, he must also show the trait. XDY XDXD XdY Carrier? (Yes or No) Has the Trait? (Yes or No) Male or Female Phenotype or Appearance of the Individual ided Questions: 1. What chromosomes will result to a normal phenotype (normal spongy po trait12