Which one of the following disorders is caused by the substitution of Glutamic acid (Glu) by Valine (Val) at the sixth position of the beta globin chain of the haemoglobin molecule ?
- Phenylketonuria
- Haemophilia
- Sickle-cell anaemia
- Thalassemia
Previous year questions with solutions · 2000 – 2026
| Year | Questions | Papers | Avg / paper | Weightage |
|---|---|---|---|---|
| 2026 | 9 | 2 | 4.5 | 8.91% ↑60.4% |
| 2025 | 3 | 1 | 3 | 5.56% ↓47.2% |
| 2024 | 12 | 2 | 6 | 10.53% ↑32.6% |
| 2023 | 5 | 1 | 5 | 7.94% ↓13.4% |
| 2022 | 12 | 2 | 6 | 9.16% ↑174.8% |
| 2021 | 2 | 1 | 2 | 3.33% ↓58.3% |
| 2020 | 4 | 1 | 4 | 8.00% ↓15.2% |
| 2019 | 5 | 1 | 5 | 9.43% ↑29.7% |
| 2018 | 4 | 1 | 4 | 7.27% ↓17.1% |
| 2017 | 5 | 1 | 5 | 8.77% ↑12.1% |
| 2016 | 9 | 2 | 4.5 | 7.83% ↑42.2% |
| 2015 | 6 | 2 | 3 | 5.50% ↓23.6% |
| 2013 | 8 | 2 | 4 | 7.21% ↑48.5% |
| 2012 | 5 | 2 | 2.5 | 4.85% ↑16.5% |
| 2011 | 4 | 2 | 2 | 4.17% ↓58.3% |
| 2010 | 9 | 2 | 4.5 | 10.00% ↑40% |
| 2009 | 4 | 1 | 4 | 7.14% ↑96.4% |
| 2008 | 2 | 1 | 2 | 3.64% ↓62.9% |
| 2007 | 5 | 1 | 5 | 9.80% ↓35.7% |
| 2006 | 9 | 1 | 9 | 15.25% ↑20.1% |
| 2005 | 8 | 1 | 8 | 12.70% ↓12.7% |
| 2004 | 8 | 1 | 8 | 14.55% ↑12.7% |
| 2003 | 8 | 1 | 8 | 12.90% ↑3.2% |
| 2002 | 8 | 1 | 8 | 12.50% ↓18.1% |
| 2001 | 9 | 1 | 9 | 15.25% ↑64.7% |
| 2000 | 5 | 1 | 5 | 9.26% |
⚠ 1 of these questions are out of the current syllabus (marked on the question).
Which one of the following disorders is caused by the substitution of Glutamic acid (Glu) by Valine (Val) at the sixth position of the beta globin chain of the haemoglobin molecule ?
The sixth mutant codon of beta globin gene causing polymerization of Haemoglobin and change in RBC shape is .
Match List I with List II : Choose the correct answer from the options given below :
If a colour blind female marries a man whose mother was also colour blind, what are the chances of her progeny having colour blindness?
Given below are two statements: In the light of the above statements, choose the correct answer from the options given below :
A normal girl, whose mother is haemophilic marries a male with no ancestral history of haemophilia. What will be the possible phenotypes of the offspring? Choose the most appropriate answer from the options given below:
In a cross between a male and female, both heterozygous for sickle cell anaemia gene, what percentage of the progeny will be diseased?
Select the correct match
A woman has an X-linked condition on one of her X chromosomes. This chromosome can be inherited by
Thalassemia and sickle cell anemia are caused due to a problem in globin molecule synthesis. Select the correct statement.
Pick out the correct statements :
Which of the following most appropriately describes haemophilia ?
If a colour-blind man marries a woman who is homozygous for normal colour vision, the probability of their son being colour-blind is
Select the incorrect statement with regard to Haemophilia :
If both parents are carriers for thalassemia, which is an autosomal recessive disorder, what are the chances of pregnancy resulting in an affected child ?
Represented below is the inheritance pattern of a certain type of traits in humans. Which one of the following conditions could be an example of this pattern ? [figure]
A normal-visioned man whose father was colour-blind, marries a woman whose father was also colour-blind. They have their first child as a daughter. What are the chances that this child would be colour-blind ?
Select the incorrect statement from the following:
Sickle-cell anaemia is:
Both sickle cell anemia and Huntington's chorea are-
If a colour blind woman marries a normal visioned man, their sons will be
Sickle cell anaemia has not been eliminated from the African population because-
G-6-P dehydrogenase deficiency is associated with haemolysis of -
A man and a woman, who do not show any apparent signs of a certain inherited disease, have seven children (2 daughters and 5 sons). Three of the sons suffer from the given disease but none of the daughters are affected. Which of the following mode of inheritance do you suggest for this disease?
Haemophilia is more commonly seen in human males than in human females because -
Which of the following is not a hereditary disease?
A woman with normal vision, but whose father was colour blind, marries a colour blind man. Suppose that the fourth child of this couple was a boy. This boy -
A male human is heterozygous for autosomal genes A and B and is also hemizygous for hemophilic gene h. What proportion of his sperms will be abh?
A normal woman, whose father was colour-blind is married to a normal man. The sons would be :-
The recessive genes located on X-chromosomes in humans are always -