Ans- He has the recessive disease allele on his x- chromosome ( XdY)
The pedigree below shows the inheritance pattern of a sex-linked allele for one family. What is...
Creating a pedigree chart from a family history and hypothesizing pattern of inheritance A family with a new disease caused by a mutant gene has been found. The family history has been collected and recorded. You will now create a pedigree chart from their family history and use the pedigree to predict the pattern of inheritance the disease follows. • Read the following family history: Patient 1 and Patient 2 visited a genetics counselor and provided their family histories. As...
For each pedigree below determine the most likely mode of inheritance and label each individual with a genotype. If you know they have a dominant phenotype, but don’t know the genotype, then label them with both possibilities. Please use the alleles A and a for autosomal modes of inheritance and XA, Xa and Ya for any types of sex-linkage (note: an “a” is only on the Y if the trait is Y-linked). Modes of inheritance are autosomal dominant, autosomal recessive,...
The pedigree shows the occurrence of a X linked recessive mendelian disease in a human family. Two unaffected family members were genotyped at a microsatellite locus and two different microsatellite alleles were observed (M1 and M2) I M1/M1 II 1 M1 M2 III 3 IV 3 5 a) Assume the disease and the microsatellite locus are completely linked. What is the genotype of individual IV-4 (give both disease and micrsatellite alleles in the genotype)? b) Assume that the disease locus...
(Q23-24) The pedigree on left shows the inheritance pattern of one human disease. • O HO 23. Which is the correct description of this disease? A. dominant and autosomal-linked B. dominant and X-chromosomal linked C. recessive and autosomal-linked D. recessive and X-chromosomal linked E. codominant and X chromosomal linked 3 24. What is the probability of an affected child from the marriage between 1 and 2? A. 0% B. 25% C. 50% D. 75% E. 100%
The pedigree below that shows a family in which an autosomal recessive disorder is present. Family members 1-2 and II-2 are affected by the disorder and have the genotype dd. A pregnancy involving Il-4 has just undergone genetic testing for a VNTR that is linked to the disease gene. The VNTR has two alleles, V1 and V2. The gel electrophoresis patterns for each family member are shown, including the VNTR genotype for 1|-4. 2 - 2 3 4 = ?...
Creating a pedigree chart from a family history and hypothesizing pattern of inheritance A family with a new disease caused by a mutant gene has been found. The family history has been collected and recorded. You will now create a pedigree chart from their family history and use the pedigree to predict the pattern of inheritance the disease follows. • Read the following family history: Patient 1 and Patient 2 visited a genetics counselor and provided their family histories. As...
Web Genotypes and phenotypes for some common single gene inheritance patterns. Inheritance Pattern Genotype Phenotype Affected Affected Not affected AA Autosomal Dominant Aa aa NN Not affected Not affected Affected Autosomal Recessive Nn nn XXN XNX Normal female Normal female Affected female Normal male Affected male Sex-linked Recessive X"X xNY X"Y Pedigree Analys is Instructions: 1. Examine the following three pedigrees. 2. Determine the most probable pattern of inheritance for each pedigree and record it in the space provided at...
(Q19-22) The pedigree on left shows the inheritance patterns of two diseases among human populations: one is indicated by a vertical line and the other indicated by a horizontal line. 3 19. Which is the correct description of the two diseases? A. dominant and autosomal-linked B. dominant and X-chromosomal linked C. recessive and autosomal-linked D. recessive and X-chromosomal linked E. codominant and X chromosomal linked 20. Which individual is heterozygous for both disease alleles? A. I-1 B. II-1 C. II-2...
QUESTION 19 Identify the pattern of inheritance in this pedigree: 10 autosomal dominant autosomal recessive X-linked dominant O X-linked recessive
In the pedigree below, what is the most likely mode of inheritance for this condition?: X-linked recessive, autosomal dominant, or autosomal recessive? Affected individuals are shown as black symbols. Based on your prediction, give the genotypes of the following individuals: I-1, I-2, II-1, II-3, II-4, III-1, III-2, III-4, IV-2, and IV-3. If you choose autosomal, use A or a; if you choose X-linked, use X^A, X^a, or Y List the proposed genotypes of the designated individuals along the side: