These various variations of a gene are referred to as alleles. For instance, two alleles may occur at one specific locus, one of which codes for the cytosine base and the other for the thymine base. One copy of the human genome is inherited from each parent. We are hence referred to as diploid organisms.
<h3>What is Allele Frequency ?</h3>
The relative frequency of an allele at a certain locus in a population, represented as a fraction or percentage, is known as gene frequency or allele frequency. The percentage of chromosomes in the population that carry that allele relative to the whole population or sample size is what is being discussed.
The frequency of an allele in a population is referred to as its allele frequency. It is calculated by dividing the number of gene copies by the number of times the allele occurs in the population. All the copies of every gene in a population make up the gene pool of that population.
<h3>What is Allele ?</h3>
Leading textbooks on genetics and evolution define an allele as a different variation of the same sequence of nucleotides at the same location on a long DNA molecule. "The chromosomal or genomic location of a gene or any other genetic element is called a locus and alternative DNA sequences at a locus are called alleles.
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This was answered before but here is the simplist answer of two differences
Mitosis has 48 chromosomes which has the diploid cells ( Time when both parents genetics chromosomes info come together.
Meiosis has 24 chromosomes which has the haploid cells ( Involve cell division and gametes come into play.
Organisms in the domains of Archaea and Bacteria reproduce with binary fission. This form of asexual reproduction and cell division is also used by some organelles within eukaryotic organisms (e.g., mitochondria).
Answer:
add a cell wall,take on rigid corners, perform a different shape,add chloroplast,make a bigger vacuole
Explanation:
thats how to make it a plant cell, sorry if i misunderstood the question
Answer: mother: XX^aa, father: X^YAa, son: X^YAa, daughter: X^X^aa.
Explanation:
Color blindness is a genetic disorder that affects the ability to distinguish colors. It is hereditary and is transmitted by an X-linked recessive allele. If a male inherits an X chromosome with the altered allele he will be color blind. In contrast, females, who have two X chromosomes, will only be colorblind if both of their X chromosomes have the altered allele. This is because <u>males have one X chromosome and one Y chromosome, while females have two X chromosomes</u>.
If the woman has normal vision, that means she cannot have both chromosomes affected. She can only have one affected chromosome (be a carrier) or none at all. Also, if she has blue eyes, which is a recessive trait, then both alleles are recessive. But the eye color is not on the X chromosome. For example, her eye color genotype can only be aa, because if she had at least one dominant allele she would have brown eye color. As for the other trait, she can be XX^, with X^ being an affected (carrier) allele or XX, i.e. both normal. So in summary, her genotype can be XXaa or XX^aa
If she has a brown-eyed male child who is also colour blind, he has inherited the allele for colour blindness from his mother, since the father does not pass on an X chromosome to the male children, only the Y. With this we can now rule out the mother's XXaa genotype since she had to have passed on her affected X^ chromosome. Then the genotype of the mother is XX^aa. And since her mother can only pass on one allele to (recessive) because she does not have allele A, the dominant that determines her brown eye color can only come from the father. So the genotype of this son is X^YAa. The female daughter has color blindness and blue eyes. So she had to inherit the affected X^ chromosome from the mother (which we already know she has) and an affected X^ chromosome from the father, because the daughter needs to inherit both affected X^ chromosomes to develop the disease. And if she also has blue eyes, she had to have inherited a recessive allele from the mother and another from the father. So with this information we can say that the father's genotype can only be X^YAa. Because the father must have both A and A alleles of the same eye color, because he passed the dominant one to the son and the recessive one to the daughter. At last, the genotype of the daughter is X^X^aa.
