Albinism is a congenital disorder resulting from the lack of which enzyme?
- tyrosinase
- xanthine oxidase
- catalase
- fructokinase.
The Correct Option is A
Solution and Explanation
Top Questions on Principles of Inheritance and Variation
- If there were 100 rose plants in a garden last year. 20 new rose plants are added through reproduction in current year. the birth rate of rose is ____ offspring per rose per year.
- CUET (UG) - 2023
- Biology
- Principles of Inheritance and Variation
- If a pink flowered snapdhagon plant is crossed with a white flowered snapdragan plant. What will be the phenotype of their progen ?
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- Biology
- Principles of Inheritance and Variation
Which of the following statements are correct about Klinefelter’s Syndrome?
A. This disorder was first described by Langdon Down (1866).
B. Such an individual has overall masculine development. However, the feminine development is also expressed.
C. The affected individual is short statured.
D. Physical, psychomotor and metal development is retarded. E. Such individuals are sterile.Choose the correct answer from the options given below:
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- Biology
- Principles of Inheritance and Variation
- Which one of the following symbols represents mating between relatives in human pedigree analysis?
- NEET (UG) - 2023
- Biology
- Principles of Inheritance and Variation
- The phenomenon of pleiotropism refers to
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- Principles of Inheritance and Variation
Questions Asked in NEET exam
- Match List I with List II:Choose the correct answer from the options given below:
List I List II A Robert May I Species-Area relationship B Alexander von Humboldt II Long term ecosystem experiment using out door plots C Paul Ehrlich III Global species diversity at about 7 million D David Tilman IV Rivet popper hypothesis - NEET (UG) - 2024
- Species diversity
- Given below are two statements: one is labelled as Assertion A and the other is labelled as Reason R.
Assertion A : The potential (V) at any axial point, at 2 m distance(r) from the centre of the dipole of dipole moment vector \(\vec{P}\) of magnitude, 4 × 10-6 C m, is ± 9 × 103 V.
(Take \(\frac{1}{4\pi\epsilon_0}=9\times10^9\) SI units)
Reason R : \(V=±\frac{2P}{4\pi \epsilon_0r^2}\), where r is the distance of any axial point, situated at 2 m from the centre of the dipole.
In the light of the above statements, choose the correct answer from the options given below :- NEET (UG) - 2024
- Magnetic Field
- Given below are two statements:
Statement I: Mitochondria and chloroplasts both double membranes bound organelles.
Statement II: Inner membrane of mitochondria is relatively less permeable, as compared chloroplast. I
In the light of the above statements, choose the mis appropriate answer from the options given below- NEET (UG) - 2024
- Cell structure and organelles
- Match List I with List II:Choose the correct answer from the options given below:
List I
List II
A Mesozoic Era I Lower invertebrates B Proterozoic Era II Fish & Amphibia C Cenozoic Era III Birds & Reptiles D Paleozoic Era IV Mammals - NEET (UG) - 2024
- Origin Of Life
- A parallel plate capacitor is charged by connecting it to a battery through a resistor. If I is the current in the circuit, then in the gap between the plates :
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- Capacitors and Capacitance
Concepts Used:
Principles of Inheritance and Variation - Mutation
A Mutation is a change in the sequence of our DNA base pairs caused by numerous environmental stimuli such as UV light or mistakes during DNA replication. Germline mutations take place in the eggs and sperm and can be passed onto offspring, whereas somatic mutations take place in body cells and are not passed on.
Types of Mutations
There are three types of mutations, which are as follows:
Silent mutation
It refers to any change in DNA sequence that has no effect on the amino acid sequence in a protein or the functions that a protein performs. There is no phenotypic indication that a mutation has occurred.
Nonsense mutation
When there is a change in the sequence of base pairs due to a point mutation, that results in a stop codon. This leads to a protein that is either shortened or non-functional.
Missense mutation
A missense mutation occurs when a point mutation causes a change in the codon, which then codes for another amino acid.
The mutation is caused by the following factors:
Internal Causes
When DNA copies incorrectly, the majority of mutations occur. Evolution occurs as a result of all of these mutations. DNA makes a copy of itself during cell division. When a copy of DNA isn't flawless, it's called a mutation since it differs somewhat from the original DNA.
External Causes
When certain chemicals or radiations are used to break down DNA, it causes the DNA to break down. The thymine dimers are broken by UV radiation, resulting in altered DNA.