Statement I: | It is not necessary that the dominant allele will be the most common allele in a population. |
Statement II: | Dominance is not an autonomous feature of an allele. |
1. | The two genes are likely to be located on different chromosomes. |
2. | All of the offspring have combinations of traits that match one of the two parents. |
3. | The genes are located on sex chromosomes. |
4. | Abnormal meiosis has occurred. |
1. | Incomplete dominance results in progeny not resembling either of the parents, whereas co-dominance results in progeny resembling both parents. |
2. | Incomplete dominance involves multiple alleles, while co-dominance does not. |
3. | Co-dominance occurs in phenotypes only, while incomplete dominance occurs in genotypes. |
4. | Incomplete dominance is a type of sex-linked inheritance, whereas co-dominance occurs in autosomes. |
1. | 1/64 | 2. | 6/64 |
3. | 15/64 | 4. | 20/64 |
1. | Identifying physical locations of genes on a chromosome. |
2. | Predicting possible traits in the offspring. |
3. | Estimating distances between genes based on the frequency of recombination. |
4. | Determining the exact sequence of nucleotides in a gene. |
1. | Alleles separate so that each gamete carries only one allele for each gene. |
2. | Genes for different traits can segregate independently during the formation of gametes. |
3. | Each allele in a pair segregates into a different sex chromosome. |
4. | Phenotypes segregate during gamete formation, leading to genetic variation. |
Assertion (A): | The strength of linkage between two genes is directly proportional to the distance between them on the chromosome. |
Reason (R): | Genes that are farther apart are less likely to be separated by recombination. |
1. | Both (A) and (R) are True and (R) is the correct explanation of (A). |
2. | Both (A) and (R) are True but (R) is not the correct explanation of (A). |
3. | (A) is True but (R) is False. |
4. | (A) is False, (R) is False. |
1. | It is caused by a mutation that results in a valine to glutamic acid substitution in hemoglobin. |
2. | It is inherited as an autosomal recessive condition. |
3. | Individuals with one sickle cell allele are typically severely affected. |
4. | Sickle cell anemia results from a deletion mutation in the hemoglobin gene. |
1. | Sickle cell anemia is caused by a single gene/point, while thalassemia is due to the deletion of one or more genes |
2. | Sickle cell anemia affects the white blood cells, whereas thalassemia affects the red blood cells |
3. | Thalassemia results in increased hemoglobin synthesis, whereas sickle cell anemia does not |
4. | Sickle cell anemia can be cured, while thalassemia cannot |