Question

inheritance—whether the disease is dominant or recessive—using this summary.
create two tables, one for each disease. for the role of the non - mutated gene column, list the general function of
the gene. for example, if the summary states that \this gene encodes a member of the atp - binding cassette (abc)
transporter\ you can write in your column \important for the use of atp.\ if you arent familiar with a word in the
summary, search the nih website for a clear definition of the term.
you can use the table provided or use the insert table button to design your own table. here is an example for one
gene:

gene	name	chromosome	sex chromosome (yes or no)	role of non - mutated gene	effect mutated gene has on body
gene	name	chromosome	sex chromosome (yes or no)	role of non - mutated gene	effect mutated gene has on body
gene 1
gene 2
gene 3
gene	name	chromosome	sex chromosome (yes or no)	role of non - mutated gene	effect mutated gene has on body
gene 1
gene 2
gene 3

Explanation:

To complete this task, we need to know the specific details of the diseases and their associated genes (such as gene names, chromosome locations, whether they are on sex chromosomes, the role of the non - mutated gene, and the effect of the mutated gene on the body). Since this information is not provided in the current problem statement, we can't fill in the tables directly.

Step - by - Step Guide to Solve (once gene/disease details are available)

1. Gather Gene/Disease Information

• For each gene related to a disease, find its official name (e.g., like CFTR for cystic fibrosis), the chromosome it is located on, whether it is on a sex chromosome (X or Y), the function of the non - mutated gene (by referring to scientific sources like the NIH website or relevant research papers), and the phenotypic effect of the mutated gene (the disease it causes and how it affects the body).

1. Fill in the Tables

• For each row in the table (corresponding to a gene), enter the gene identifier (if any), the gene name, the chromosome number, whether it is on a sex chromosome (Yes/No), the role of the non - mutated gene (in simple terms, e.g., "important for cell signaling" or "involved in DNA repair"), and the effect of the mutated gene on the body (e.g., "causes a neurodegenerative disorder" or "leads to a metabolic disease").

Since the necessary gene and disease details are missing, we can't provide the filled - in tables. Please provide the details of the genes and diseases (such as their names, chromosome locations, gene functions, and disease phenotypes) to complete this task.

Answer:

To complete this task, we need to know the specific details of the diseases and their associated genes (such as gene names, chromosome locations, whether they are on sex chromosomes, the role of the non - mutated gene, and the effect of the mutated gene on the body). Since this information is not provided in the current problem statement, we can't fill in the tables directly.

Step - by - Step Guide to Solve (once gene/disease details are available)

1. Gather Gene/Disease Information

• For each gene related to a disease, find its official name (e.g., like CFTR for cystic fibrosis), the chromosome it is located on, whether it is on a sex chromosome (X or Y), the function of the non - mutated gene (by referring to scientific sources like the NIH website or relevant research papers), and the phenotypic effect of the mutated gene (the disease it causes and how it affects the body).

1. Fill in the Tables

• For each row in the table (corresponding to a gene), enter the gene identifier (if any), the gene name, the chromosome number, whether it is on a sex chromosome (Yes/No), the role of the non - mutated gene (in simple terms, e.g., "important for cell signaling" or "involved in DNA repair"), and the effect of the mutated gene on the body (e.g., "causes a neurodegenerative disorder" or "leads to a metabolic disease").

Since the necessary gene and disease details are missing, we can't provide the filled - in tables. Please provide the details of the genes and diseases (such as their names, chromosome locations, gene functions, and disease phenotypes) to complete this task.