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In sickle cell anaemia, the sequence of ...

In sickle cell anaemia, the sequence of amino acid from first to seventh position of `beta`-chain of haemoglobin S (HbS) is

A

His, Leu, Thr, Pro, Glu, Val, Val

B

Val, His, Leu, Thr, Pro, Glu,Glu

C

Thr, His, Pro, Val, Pro, Val, Glu

D

Glu, His, Leu, Pro, Val, Glu, Glu

Text Solution

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The correct Answer is:
C

In sickle-cell anaemia, the correct seqence of amino acid from 1-7th position of the B-chain haemoglobins is Val - His - Leu - Thr - Pro - Val - Glu
1 2 3 4 5 6 7
It occurs when amino acid glutamine (Glu)at position 6 is replaced by amino acid valine (Val)
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ARIHANT NEET-HUMAN GENETICS-Chapter Exercise (c) Medical entrances gallery (Collection of questions asked in NEET & Various Medical Entrance Exams)
  1. Which of the following is correctly matched?

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  2. A person affected with phenylketonuria lacks an enzyme that converts t...

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  3. In sickle cell anaemia, the sequence of amino acid from first to seven...

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  4. Anish is having colour blindness and married to Sheela, who is not col...

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  5. The genotype of a person suffering from Klinefelter's symdrome is

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  6. In alpha thalasssemia the gene HBAI is located on chromosome

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  7. Sickle-cell anaemia is caused due to the substitution of :

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  8. Down's syndrome is an example

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  9. In down's syndrome (Mongolism), each cell has how many chromosomes?

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  10. In the given pedigree, the shaded individuals are homozygous recessive...

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  11. Haemophilia is related to

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  12. The gene of sickle cell anaemia is inherited by

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  13. Represented below is the inheritance pattern of a certain type of trai...

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  14. A normal - visioned man whose father was colourblind. Theiy have their...

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  15. A woman with albinic father marries an albinic man. The proportion of ...

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  16. Which following pair of diseases is caused by two genes located on hum...

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  17. If father shown normal gentype and mother shown a carrier trait for ha...

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  18. Cri-du-chat syndrome in humans is caused by the :

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  19. Colour blindness is caused due to

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  20. The chromosomal condition in Turner's syndrome is or A human female ...

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