An STR on chromosome 9 is immediately adjacent to a gene involved in a dominant blood disorder (only one copy of the mutation is required for the disease). Thus, in a family with a known mutation in the disorder-causing gene, inheritance of the STR can be used to diagnose the disorder. There are four different alleles of the STR (A, B, C and D), each with different numbers of GATCTCG repeats. The A allele has 10 repeats, the B allele has 19 repeats, the Callele has 25 repeats, and the D allele has 13 repeats. Part 1. Lane 1 of the gel shown below indicates the locations of PCR products corresponding to all four STR alleles when run together in one lane. DNA was loaded into the wells at the top of the gel. Lane 1 Janavi Mehmet Prita Kamu Ravi Shreeta List the location of each allele by its letter in order from top (- side of gel) to bottom (+ side of gel). BIUA - A - I E E 3 x' x, E E 14pt Paragraph
An STR on chromosome 9 is immediately adjacent to a gene involved in a dominant blood disorder (only one copy of the mutation is required for the disease). Thus, in a family with a known mutation in the disorder-causing gene, inheritance of the STR can be used to diagnose the disorder. There are four different alleles of the STR (A, B, C and D), each with different numbers of GATCTCG repeats. The A allele has 10 repeats, the B allele has 19 repeats, the Callele has 25 repeats, and the D allele has 13 repeats. Part 1. Lane 1 of the gel shown below indicates the locations of PCR products corresponding to all four STR alleles when run together in one lane. DNA was loaded into the wells at the top of the gel. Lane 1 Janavi Mehmet Prita Kamu Ravi Shreeta List the location of each allele by its letter in order from top (- side of gel) to bottom (+ side of gel). BIUA - A - I E E 3 x' x, E E 14pt Paragraph
Human Heredity: Principles and Issues (MindTap Course List)
11th Edition
ISBN:9781305251052
Author:Michael Cummings
Publisher:Michael Cummings
Chapter11: Genome Alterations: Mutation And Epigenetics
Section: Chapter Questions
Problem 16QP: Familial retinoblastoma, a rare autosomal dominant defect, arose in a large family that had no prior...
Related questions
Question
Please help me since I am not too sure
Expert Solution
This question has been solved!
Explore an expertly crafted, step-by-step solution for a thorough understanding of key concepts.
This is a popular solution!
Trending now
This is a popular solution!
Step by step
Solved in 2 steps
Knowledge Booster
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, biology and related others by exploring similar questions and additional content below.Recommended textbooks for you
Human Heredity: Principles and Issues (MindTap Co…
Biology
ISBN:
9781305251052
Author:
Michael Cummings
Publisher:
Cengage Learning
Human Heredity: Principles and Issues (MindTap Co…
Biology
ISBN:
9781305251052
Author:
Michael Cummings
Publisher:
Cengage Learning