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Class 12 Biology Chapter 5 MCQs with Answers and Ads


Class 12 Biology Chapter 5: Principles of Inheritance and Variation – 100 MCQs with Answers



1. The father of genetics is:

A) Darwin
B) Mendel
C) Morgan
D) Watson
Answer: B) Mendel
2. Mendel’s experiments were carried out on:

A) Maize
B) Sunflower
C) Pea plant
D) Wheat
Answer: C) Pea plant
3. Study of inheritance is called:

A) Genetics
B) Evolution
C) Ecology
D) Variation
Answer: A) Genetics
4. Law of segregation is also known as:

A) Law of purity of gametes
B) Law of dominance
C) Law of assortment
D) Law of linkage
Answer: A) Law of purity of gametes
5. The phenotypic ratio of dihybrid cross is:

A) 2:1
B) 1:2:1
C) 9:3:3:1
D) 3:1
Answer: C) 9:3:3:1
6. Test cross is between:

A) F1 and F1
B) F1 and recessive parent
C) F2 and dominant parent
D) None
Answer: B) F1 and recessive parent
7. Who rediscovered Mendel’s work?

A) Lamarck
B) Darwin
C) Correns, de Vries & Tschermak
D) Watson
Answer: C) Correns, de Vries & Tschermak
8. Chromosome theory of inheritance was proposed by:

A) Watson & Crick
B) Sutton & Boveri
C) Bateson
D) Morgan
Answer: B) Sutton & Boveri
9. Genes are located on:

A) Ribosomes
B) Chromosomes
C) Mitochondria
D) Centrioles
Answer: B) Chromosomes
10. Alternate forms of a gene are called:

A) Genotype
B) Phenotype
C) Alleles
D) Loci
Answer: C) Alleles



11. A cross between tall (TT) and dwarf (tt) pea plants produces:

A) Tall and dwarf
B) Only tall
C) Only dwarf
D) All medium
Answer: B) Only tall
12. The term ‘pure line’ was coined by:

A) Bateson
B) Morgan
C) Johannsen
D) Mendel
Answer: C) Johannsen
13. In incomplete dominance, F1 phenotype is:

A) Like dominant
B) Like recessive
C) Intermediate
D) Varied
Answer: C) Intermediate
14. The number of chromosomes in human somatic cell:

A) 23
B) 46
C) 48
D) 44
Answer: B) 46
15. Sickle cell anaemia is due to:

A) Chromosome deletion
B) Point mutation
C) Frame shift
D) Polyploidy
Answer: B) Point mutation
16. Colour blindness is a:

A) Y-linked trait
B) Sex-limited trait
C) Sex-linked trait
D) Cytoplasmic trait
Answer: C) Sex-linked trait
17. ABO blood group is an example of:

A) Polygenic inheritance
B) Codominance
C) Multiple alleles
D) Epistasis
Answer: C) Multiple alleles
18. The gene for haemophilia is located on:

A) X chromosome
B) Y chromosome
C) Both X and Y
D) Autosomes
Answer: A) X chromosome
19. The trait which always appears in F1 is:

A) Dominant
B) Recessive
C) Intermediate
D) Lethal
Answer: A) Dominant
20. Linkage was first discovered by:

A) Mendel
B) Morgan
C) De Vries
D) Correns
Answer: B) Morgan



21. The genotype of a male with haemophilia is:

A) XhXh
B) XhY
C) XHXh
D) XHY
Answer: B) XhY
22. The 9:3:3:1 ratio is possible in a cross involving:

A) One pair of alleles
B) Two pairs of alleles
C) Three pairs
D) None
Answer: B) Two pairs of alleles
23. Phenotype means:

A) Physical appearance
B) Gene composition
C) Gamete
D) None
Answer: A) Physical appearance
24. Mendel’s factor is now called:

A) DNA
B) Gene
C) RNA
D) Enzyme
Answer: B) Gene
25. Chromosomal disorder among following:

A) Sickle cell
B) Cystic fibrosis
C) Down’s syndrome
D) Albinism
Answer: C) Down’s syndrome
26. Turner’s syndrome individuals are:

A) XO
B) XXY
C) XYY
D) XXX
Answer: A) XO
27. In Down’s syndrome, the karyotype shows:

A) Trisomy 21
B) Monosomy 13
C) Trisomy 18
D) Monosomy 15
Answer: A) Trisomy 21
28. A man with blood group AB marries a woman with O. Offspring’s groups:

A) A, B
B) AB, O
C) AB, A
D) A, B, AB
Answer: A) A, B
29. The probability of a boy being colour-blind if his mother is a carrier:

A) 0%
B) 25%
C) 50%
D) 75%
Answer: C) 50%
30. A change in a single nucleotide is a:

A) Deletion
B) Inversion
C) Point mutation
D) Frame shift
Answer: C) Point mutation



31. The 3:1 ratio is possible in:

A) Monohybrid cross
B) Dihybrid cross
C) Trihybrid cross
D) Back cross
Answer: A) Monohybrid cross
32. Human sex chromosome pair is:

A) 22
B) 23
C) 46
D) 21
Answer: B) 23
33. Crossing over occurs during:

A) Metaphase I
B) Prophase I
C) Anaphase I
D) Telophase I
Answer: B) Prophase I
34. Blood group O is:

A) Universal donor
B) Universal recipient
C) Recessive
D) None
Answer: A) Universal donor
35. Gene for colour blindness is:

A) Autosomal
B) Sex-linked
C) Dominant
D) Y-linked
Answer: B) Sex-linked
36. Genetic makeup of an organism is:

A) Phenotype
B) Genotype
C) Allele
D) Gene
Answer: B) Genotype
37. Haemophilia is more common in males because:

A) Gene is on X chromosome
B) Y chromosome
C) Both
D) Z chromosome
Answer: A) Gene is on X chromosome
38. The karyotype of person with Down’s syndrome:

A) 44+XY
B) 45+XX
C) 47 chromosomes
D) 42+XY
Answer: C) 47 chromosomes
39. Genotype of a carrier female for colour blindness:

A) XX
B) XcX
C) XY
D) XcY
Answer: B) XcX
40. Mendelian disorder among following:

A) Haemophilia
B) Down’s syndrome
C) Turner’s syndrome
D) Klinefelter’s syndrome
Answer: A) Haemophilia



41. Number of Barr body in normal female is:

A) 0
B) 1
C) 2
D) 3
Answer: B) 1
42. A universal recipient has blood group:

A) AB
B) A
C) B
D) O
Answer: A) AB
43. Which chromosome is not an autosome in human:

A) 1
B) 5
C) X
D) 12
Answer: C) X
44. Chromosomes are made up of:

A) DNA & protein
B) RNA
C) Only DNA
D) Fat
Answer: A) DNA & protein
45. Hemoglobin S is seen in:

A) Sickle cell anaemia
B) Cystic fibrosis
C) Thalassemia
D) Down’s syndrome
Answer: A) Sickle cell anaemia
46. Study of chromosomes is:

A) Pedigree analysis
B) Karyotyping
C) Mutagenesis
D) Genetics
Answer: B) Karyotyping
47. Mendelian ratio for incomplete dominance:

A) 3:1
B) 2:1
C) 1:2:1
D) 9:3:3:1
Answer: C) 1:2:1
48. Point mutation example is:

A) Sickle cell anaemia
B) Down’s syndrome
C) Klinefelter’s
D) Turner’s
Answer: A) Sickle cell anaemia
49. Thalassemia affects:

A) Globin
B) Albumin
C) Insulin
D) Collagen
Answer: A) Globin
50. The chromosomal basis of sex determination was explained by:

A) Sutton
B) Mendel
C) Morgan
D) Darwin
Answer: A) Sutton



51. Polygenic inheritance controls:

A) Skin color
B) Blood group
C) Eye color
D) Both A & C
Answer: D) Both A & C
52. Mutation theory was proposed by:

A) Mendel
B) De Vries
C) Morgan
D) Darwin
Answer: B) De Vries
53. In humans, sex-linked genes are mostly found on:

A) X chromosome
B) Y chromosome
C) Both
D) Autosomes
Answer: A) X chromosome
54. Phenotypic ratio in F2 generation of a monohybrid cross is:

A) 9:3:3:1
B) 3:1
C) 1:2:1
D) 1:1
Answer: B) 3:1
55. Sex determination in humans depends on:

A) Father
B) Mother
C) Both
D) Grandparents
Answer: A) Father
56. Male with XXY chromosomes is:

A) Turner’s syndrome
B) Klinefelter’s syndrome
C) Down’s syndrome
D) Normal
Answer: B) Klinefelter’s syndrome
57. Chromosome number in Turner’s syndrome:

A) 46
B) 45
C) 47
D) 48
Answer: B) 45
58. Autosomal recessive disorder is:

A) Haemophilia
B) Thalassemia
C) Colour blindness
D) Turner’s
Answer: B) Thalassemia
59. Chromosomal mutation includes:

A) Deletion
B) Inversion
C) Duplication
D) All
Answer: D) All
60. Mendel’s third law is:

A) Law of segregation
B) Law of dominance
C) Law of independent assortment
D) Law of linkage
Answer: C) Law of independent assortment



61. Human egg cell contains:

A) 23 chromosomes
B) 24 chromosomes
C) 22 chromosomes
D) 20 chromosomes
Answer: A) 23 chromosomes
62. The genetic constitution AA is called:

A) Homozygous dominant
B) Homozygous recessive
C) Heterozygous
D) None
Answer: A) Homozygous dominant
63. Homologous chromosomes are:

A) Identical chromosomes
B) Pair of chromosomes carrying same gene loci
C) Sex chromosomes only
D) Different chromosomes
Answer: B) Pair of chromosomes carrying same gene loci
64. Inheritance of height in humans is:

A) Polygenic
B) Monogenic
C) Codominant
D) Linked
Answer: A) Polygenic
65. A gene present on Y chromosome is:

A) Holandric
B) Sex-linked
C) Autosomal
D) None
Answer: A) Holandric
66. Sickle cell disease is not cured because:

A) Recessive allele
B) Dominant allele
C) Mutation
D) Both A & C
Answer: D) Both A & C
67. XXY karyotype results in:

A) Turner
B) Down
C) Klinefelter
D) Triple X
Answer: C) Klinefelter
68. A man with hemophilia marries a normal woman, their sons will be:

A) All normal
B) All hemophilic
C) 50% chance
D) All carrier
Answer: A) All normal
69. The number of pairs of sex chromosomes in humans:

A) 2
B) 1
C) 23
D) 22
Answer: B) 1
70. Down’s syndrome cause is:

A) Trisomy 21
B) Monosomy 21
C) Trisomy X
D) Deletion 21
Answer: A) Trisomy 21



71. The number of alleles controlling blood groups in humans:

A) 1
B) 2
C) 3
D) 4
Answer: C) 3
72. Allosomes are:

A) Autosomal chromosomes
B) Sex chromosomes
C) Both
D) None
Answer: B) Sex chromosomes
73. Phenylketonuria is due to:

A) Enzyme deficiency
B) Chromosomal aberration
C) Trisomy
D) Karyotype abnormality
Answer: A) Enzyme deficiency
74. Thalassemia is:

A) Sex linked
B) Autosomal dominant
C) Autosomal recessive
D) Holandric
Answer: C) Autosomal recessive
75. Mendelian inheritance is shown by:

A) Sickle cell anaemia
B) Haemophilia
C) PKU
D) All
Answer: D) All
76. Pedigree analysis is useful for:

A) Human genetics
B) Animal genetics
C) Plant genetics
D) All
Answer: D) All
77. Male with X chromosome and no Y:

A) Sterile
B) Turner syndrome
C) Klinefelter syndrome
D) Normal
Answer: B) Turner syndrome
78. Who coined the term genetics?

A) Bateson
B) Mendel
C) Morgan
D) Darwin
Answer: A) Bateson
79. Gene for sickle cell is located on chromosome:

A) 1
B) 2
C) 11
D) 21
Answer: C) 11
80. Number of linkage groups in humans:

A) 22
B) 23
C) 24
D) 46
Answer: B) 23



81. Inheritance of genes located on mitochondria is:

A) Paternal
B) Maternal
C) Both
D) None
Answer: B) Maternal
82. Drosophila is ideal for genetics studies because:

A) Short life cycle
B) Large size
C) Sex chromosomes
D) Polyploidy
Answer: A) Short life cycle
83. Y-linked inheritance is called:

A) Holandric
B) Autosome
C) Sex-linked
D) Dominant
Answer: A) Holandric
84. Crossing over increases:

A) Linkage
B) Variability
C) Mutation
D) Chromosome number
Answer: B) Variability
85. Sickle cell trait is advantageous against:

A) Malaria
B) Anemia
C) Thalassemia
D) Diabetes
Answer: A) Malaria
86. Presence of three X chromosomes is:

A) Turner
B) Down
C) Superfemale
D) Klinefelter
Answer: C) Superfemale
87. The number of total chromosomes in Turner syndrome:

A) 46
B) 45
C) 44
D) 43
Answer: B) 45
88. The allele responsible for sickling is:

A) HbA
B) HbS
C) HBA1
D) HBA2
Answer: B) HbS
89. Father to son inheritance is seen in:

A) X-linked
B) Y-linked
C) Autosomal
D) Mitochondrial
Answer: B) Y-linked
90. Down’s syndrome can be detected by:

A) Karyotyping
B) Amniocentesis
C) Both
D) None
Answer: C) Both



91. Gene is a segment of:

A) RNA
B) DNA
C) Chromosome
D) Centrosome
Answer: B) DNA
92. Barr body is found in:

A) Males
B) Females
C) Both
D) None
Answer: B) Females
93. The number of Barr bodies in Klinefelter’s syndrome:

A) 0
B) 1
C) 2
D) 3
Answer: B) 1
94. Genes located on same chromosome are called:

A) Linked genes
B) Alleles
C) Locus
D) Chromatids
Answer: A) Linked genes
95. ABO group is located on chromosome:

A) 15
B) 9
C) 22
D) 13
Answer: B) 9
96. Colour blindness is absent in:

A) Girls
B) Boys
C) Females
D) None
Answer: A) Girls
97. Which is not a Mendelian disorder?

A) Sickle cell
B) Thalassemia
C) Down’s syndrome
D) Colour blindness
Answer: C) Down’s syndrome
98. Genetic disorder with trisomy:

A) Down’s syndrome
B) Sickle cell
C) Cystic fibrosis
D) Haemophilia
Answer: A) Down’s syndrome
99. Y-linked trait is transmitted from:

A) Father to son
B) Mother to son
C) Father to daughter
D) Mother to daughter
Answer: A) Father to son
100. Genotype of normal female:

A) XY
B) XX
C) YY
D) XO
Answer: B) XX

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