Answer:
Let us consider that A signifies the dominant allele and letter a signifies the recessive allele. The dominant allele, A would demonstrate normal phenotype, on the other hand, the recessive allele, a would be accountable for the disease. The possibilities of genotypes and phenotypes would be AA demonstrating normal homozygous individual, Aa demonstrating normal heterozygous individual, and aa demonstrating homozygous individual carrying the disease.
Based on the given question, the genotype of the individual would be Aa, due to the existence of the dominant allele, normal phenotype would be demonstrated by the individual. In case if the deletion of A allele takes place from the genotype, the left a allele would possess the tendency to show its effect and the expression of the recessive phenotype will take place.
Hemizygous refers to the condition in which only one allele is found in a diploid organism, and the organism within which it takes place is known as hemizygote.
Answer:
point mutation missense mutation silent mutation non sense mutation
Explanation:
point mutation it change one base of DNA in this case nucleotide substitution occur like sickle cell missense mutation in this case replacement of one nucleotide nonsense mutation cause the replacement of codon silent mutation does not change the sequence of protein because of new triplets codes for the same amino acid
Homeostasis can be defined as the state of maintenance of the constant internal conditions by the living organisms. The homeostasis is maintained by the body so that it may function properly. The homeostasis will be disturbed by the reduced intake of the food and water. Healthy intake of water and food is essential in maintaining the homeostasis of the body. The elevated or depressed blood pH along with extreme body temperatures will also disturb the homeostasis of the body making the person sick. Moreover, certain infectious organisms also alters the homeostasis of the body.
Hence, all the options are correct.
Answer:
Explanation:
The homozygous recessive individual can only produce 1 type of gamete (<em>aabb</em>).
The heterozygous individual can produce 8 types of gametes, of which 2 are parental and the rest are recombinant.
Genetic distance (m.u.) = Frequency of Recombination (%)
If the distance between genes A and B is 50 m.u., 50% of the gametes produced by the heterozygous individual, and therefore the offspring, will have recombinant phenotypes.
Without knowing that the genes are located on the same chromosomes, I'd think they are on different chromosomes, because you would get the same result: 50% recombinant offspring.
Whenever the genes on the same chromosome are separated by at least 50 m.u., or they are in different chromosomes, crossing over between them can happen with no restrictions and they will behave as independent of one another.
True I study this last semester
