Complete question:
Imagine that a newly discovered, recessively inherited disease is expressed only in individuals with type O blood, although the disease and blood group are independently inherited.
A normal man with type A blood and a normal woman with type B blood have already had one child with the disease. The woman is now pregnant for a second time.
Assuming that both parents are heterozygous for the gene that causes the disease, what is the probability that the second child will also have the disease? Express your answer as a fraction using the slash symbol and no spaces (for example, 1/2).
Answer:
The probability that the second child will also have the disease is 1/16.
Explanation:
<u>Available data:</u>
- Two genes independently inherited: one for blood type, the other for disease
- Man with type A blood x Woman with type B blood
- Both parents are heterozygous for the gene that causes the disease; Dd
If the man has A blood, and the woman has B blood, and they already have an affected child, this means that they must be heterozygous for blood type too.
Cross:
Parentals) AiDd x BiDd
Gametes) AD Ad iD id BD Bd iD id
Punnett square) AD Ad iD id
BD ABDD ABDd BiDD BiDd
Bd ABDd ABdd BiDd Bidd
iD AiDD AiDd iiDD iiDd
id AiDd Aidd iiDd iidd
F1) <u>Genotype</u>:
1/16 ABDD
2/16 ABDd
1/16 ABdd
1/16 AiDD
1/16 BiDD
2/16 AiDd
2/16 BiDd
1/16 Aidd
1/16 Bidd
1/16 iiDD
2/16 iiDd
1/16 iidd
<u>Phenotype:</u>
3/16 A/B normal
4/16 A normal
4/16 B normal
3/16 0 normal
1/16 0 affected by the disease.
We know that height in humans is a polygenic trait because it has a lot of variation. The height gene is controlled by at minimum three genes with six different alleles. If all of these alleles are dominant for the tall gene you will be tall if you are dominant for the short gene you will be short if there is no clear dominance between the two genes you will fall somewhere in the middle.
I believe these are the answers:) best of luck!
Molecular biologists are interested in things like the level of gene expression (how much protein or RNA is present at any given time), which molecules are directly touching each other inside the cell, etc. ... Cell biology techniques, on the other hand, want to know what's going on inside intact cells.
( Try to see which one sounds best after reading this)
In a membrane, the tail of the phospholipids in one monolayer face the tail of the phospholipids in the other monolayer.
<h3>
What is cell membrane?</h3>
- The cell membrane is a biological membrane that separates and protects the inside of all cells from the outside environment.
- It is also known as the plasma membrane (PM), cytoplasmic membrane or plasmalemma (extracellular space).
- The cell membrane consists of a lipid bilayer, which is made up of two layers of phospholipids interwoven with cholesterol (a lipid component) to maintain proper membrane fluidity at different temperatures.
- Furthermore, membranes are composed of membrane proteins, such as those that cannot be separated across the membrane and function as membrane transporters, and peripheral proteins that simply attach to the outer membrane of the cell and function as membrane transporters. enzymes to help the cell interact with its environment.
- The integrated glycolipids of the outer lipid layer perform a similar function.
To learn more about the membrane, refer to the following link:
brainly.com/question/1768729
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