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Class12 Inheritance Variation Important QA

The document provides a series of questions and answers related to the principles of inheritance and variation in biology, specifically tailored for Class 12 students. It covers key concepts such as alleles, genotype, phenotype, Mendel's laws, blood group inheritance, and chromosomal disorders. The content is structured into 2, 3, and 5 mark questions, offering concise explanations and examples for each topic.

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0% found this document useful (0 votes)
4 views4 pages

Class12 Inheritance Variation Important QA

The document provides a series of questions and answers related to the principles of inheritance and variation in biology, specifically tailored for Class 12 students. It covers key concepts such as alleles, genotype, phenotype, Mendel's laws, blood group inheritance, and chromosomal disorders. The content is structured into 2, 3, and 5 mark questions, offering concise explanations and examples for each topic.

Uploaded by

kasajana888
Copyright
© All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd

Class 12 Biology: Principles of Inheritance and

Variation
Extended 2, 3 and 5 Mark Questions with Answers
2 Mark Questions and Answers
1. Define allele.
Ans: Alternative forms of the same gene are called alleles.
2. What is genotype?
Ans: The genetic constitution of an organism.
3. What is phenotype?
Ans: The observable characteristics of an organism.
4. State Mendel's Law of Dominance.
Ans: One allele is dominant and expresses itself in a heterozygote.
5. What is a test cross?
Ans: A cross with a homozygous recessive parent to determine genotype.
6. What are multiple alleles?
Ans: More than two alternative forms of a gene in a population.
7. What is mutation?
Ans: A sudden heritable change in genetic material.
8. What are homologous chromosomes?
Ans: Chromosomes similar in size, shape and gene arrangement.
9. What is codominance?
Ans: Both alleles express equally in a heterozygous condition.
10. Differentiate genotype and phenotype.
Ans: Genotype is genetic makeup; phenotype is outward appearance.
3 Mark Questions and Answers
1. Explain ABO blood group inheritance.
Ans: ABO blood groups are controlled by IA, IB and i. IA and IB are codominant and both dominate
over i.
2. Explain Mendel's Law of Segregation.
Ans: Alleles occur in pairs and separate during gamete formation. Each gamete receives one allele.
3. Describe a monohybrid cross.
Ans: A cross involving one pair of contrasting traits. F2 ratio is 3:1.
4. What is pedigree analysis?
Ans: Study of inheritance patterns through family trees.
5. Explain linkage and recombination.
Ans: Linked genes tend to be inherited together. Recombination produces new gene combinations.
6. What is incomplete dominance? Give an example.
Ans: Neither allele is completely dominant. Example: Snapdragon flowers.
7. What is sex determination in humans?
Ans: Females are XX and males are XY. Male gametes determine the sex of offspring.
8. What are chromosomal disorders?
Ans: Disorders caused by abnormal chromosome number or structure, e.g., Down syndrome.
5 Mark Questions and Answers
1. Explain Mendel's monohybrid cross.
Ans: Mendel crossed TT (tall) with tt (dwarf). F1 plants were all tall (Tt). Selfing produced F2 with 3
tall : 1 dwarf phenotypic ratio and 1:2:1 genotypic ratio.

2. Explain Mendel's dihybrid cross.


Ans: Mendel crossed plants differing in two traits. F2 generation showed a 9:3:3:1 ratio, proving
independent assortment.

3. Explain the chromosomal theory of inheritance.


Ans: Genes are located on chromosomes. Chromosomes occur in pairs, segregate during meiosis
and reunite at fertilization.

4. Describe Down syndrome.


Ans: Down syndrome is caused by trisomy 21. Affected individuals have 47 chromosomes and
characteristic physical and developmental features.

5. Explain ABO blood group inheritance in detail.


Ans: Three alleles IA, IB and i control blood groups. IA and IB are codominant while i is recessive.
This produces A, B, AB and O blood groups.

6. Write a note on Turner syndrome and Klinefelter syndrome.


Ans: Turner syndrome is 45,X. Klinefelter syndrome is 47,XXY. Both are sex chromosome
abnormalities.

7. Explain sex determination in humans with a diagram.


Ans: Humans follow the XX-XY mechanism. Females produce X gametes while males produce X
and Y gametes. Fertilization determines sex.

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