Check 2
Check 2
Column-I Column-II
(A) Genes (1) Slightly
different
forms of the
same gene
(B) Alleles (2) Genetic
composition
of an
organism
(C) Genotype (3) Physical
appearance
of an
organism
(D) Phenotype (4) Unit of
inheritance
Codes- A) A – tt, B – Tt
B) A – Tt, B – tt
A B C D
C) A – TT, B – TT
A) 4 1 2 3
D) A – Tt, B – Tt
B) 1 4 3 2
33. Choose the incorrect statement about
C) 3 2 4 1
D) 2 3 1 4 Mendel’s monohybrid cross.
31. A cross that is performed for the study A) The recessive parental trait is
of a single character is expressed without any blending in
A) dihybrid cross F2 generation.
B) test cross B) The alleles of parental pair segregate
C) monohybrid cross from each other and both alleles are
D) back cross transmitted to a gamete.
C) The segregation of alleles is a
32. The given figure is the diagrammatic random process.
representation of a monohybrid cross. D) There is a 50% chance of a gamete
In the figure, some plants are containing either allele.
mentioned as A and B. What will be the 34. The production of gametes by the
genotype of these plants? parents the formation of zygotes, the F1
and F2 plants, can be understood by
using [NEET Odisha-2019]
A) Wenn diagram
B) Pie diagram
C) A pyramid diagram
D) Punnett square
Chapter – 5 DPP
35. Select the correct statement. [NEET- C) It also explains the proportion of 3:
2018] 1 obtained in F2-generation.
A) Franklin Stahl coined the term D) It states that characters are
‘linkage’. controlled by discrete units called
B) Punnett square was developed by a factors.
British scientist. 41. Match Column-I with Column-II and
C) Spliceosomes take part in choose the correct option from the
translation. codes given below.
D) Transduction was discovered by S
Altman. Column-I Column-II
(A) First law of (1) Law of
36. In the test cross, organism whose
inheritance segregation
genotype is to be determined, is crossed
(B) Second law of (2) 3: 1
with the inheritance
A) recessive parent (C) Monohybrid (3) Law of
B) dominant parent cross dominance
C) both parents one by one (D) Test cross (4) 1: 1
D) none of these
37. On crossing two tall plants, in F1-
generation few dwarf offspring were Codes-
obtained. What would be the genotype A B C D
of the both the parent? [NCERT A) 3 1 2 4
Exemplar] B) 1 3 4 2
A) TT and Tt C) 2 3 1 4
B) Tt and Tt D) 4 2 3 1
C) TT and TT 42. The second law of inheritance, i.e., law
D) TT and tt of segregation is based on the fact that
38. Based on his observations of A) alleles do not show any blending.
monohybrid cross, Mendel proposed B) both characters are recovered as
which law of inheritance? such in F2 generation.
A) Law of dominance C) one allele dominates the other allele.
B) Law of segregation D) Both (A) and (B)
C) Law of independent assortment 43. The factor controlling any character is
D) Both (A) and (B) discrete and independent. It was
39. According to Mendel, characters are concluded on the basis of [NCERT
controlled by discrete units called Exemplar]
A) genes A) results of F3-generation of a cross.
B) factors B) observations of a cross made
C) alleles between the plants having two
D) allelomorph contrasting traits where offspring
40. Choose the incorrect statement about shows only one trait without any
law of dominance. blending.
A) It is used to explain the expression C) self-pollination of F1-offspring.
of only one of the parental D) cross pollination of parental
characters in a monohybrid cross in generations.
F1-generation.
B) It does not explain the expression of
both parental characters in F2-
generation.
Chapter – 5 DPP
62. Assertion: The pink flower of dog plant B) the alleles of two genes are
show incomplete dominance. interacting with each other.
Reason: In pink flowers, both alleles are C) it is a case of multiple allelism.
expressed equally. D) the alleles of two genes are
A) Both assertion and reason are true segregating independently.
and reason is the correct 68. The numbers of phenotypes and
explanation of assertion. genotypes in F2 generation of a
B) Both assertion and reason are true Mendelian dihybrid cross are [NCERT
but reason is not correct Exemplar]
explanation of assertion. A) phenotypes 4: genotypes 16
C) Assertion is true, but reason is false. B) phenotypes 4: genotypes 8
D) Both assertion and reason are false. C) phenotypes 9: genotypes 4
63. Assertion: A person having IAIB D) phenotypes 4: genotypes 9
genotype has AB blood group. 69. Mendel’s law of independent
Reason: IA and IB alleles are co- assortment is true for the genes
dominant situated on the [NCERT Exemplar]
A) Both assertion and reason are true A) same chromosome
and reason is the correct B) non-homologous chromosomes
explanation of assertion. C) homologous chromosomes
B) Both assertion and reason are true D) extra nuclear genetic element
but reason is not correct 70. Genes A and B are linked. The F1
explanation of assertion. heterozygote of a dihybrid cross
C) Assertion is true, but reason is false. involving these genes is crossed with
D) Both assertion and reason are false. homozygous recessive parental type
(aabb). What would be the ratio of
Inheritance of two Genes offspring in the next generation?
[NCERT Exemplar]
64. Crosses that are performed to study A) 1: 1
two contrasting characters at a time are B) 1: 1: 1: 1
called C) 9: 3: 3: 1
A) monohybrid cross D) 3: 1
B) dihybrid cross 71. Mendel’s work remained unrecognized
C) test cross for many years. Find out the true
D) back cross reason for the same.
65. The phenotypic ratio obtained by (I) Mendel’s concept of genes was
Mendel in his dihybrid cross was not accepted by his
A) 1 : 2 : 1 : 2 contemporaries as an
B) 3 : 2 : 2 : 1 explanation for the continuous
C) 9 : 3 : 3 : 1 variation seen in nature.
D) 2 : 3 : 1 : 2 (II) The approach of using
66. The third law of inheritance proposed mathematics was new and
by Mendel is unacceptable by other biologists.
A) Law of dominance (III) He could not provide any
B) Law of independent assortment physical proof for the existence
C) Law of incomplete dominance of factors. (IV) Communication
D) Law of segregation was not easy in those days and
67. The ratio 9: 3: 3: 1 of a dihybrid cross his work could not be widely
denotes that [NCERT Exemplar] published.
A) it is a multigenic inheritance. A) I and II
Chapter – 5 DPP
82. Among the following which will not 85. The concept of genetic map was given
cause variations among siblings? by
[NCERT Exemplar] A) de Vries
A) Linkage B) Morgan
B) Independent assortment of genes C) Sturtevant
C) Crossing over D) Mendel
D) Mutation 86. Assertion: Mendel proposed the law of
83. Match Column-I with Column-II and independent assortment on the basis of
choose the correct answer from the results of dihybrid cross.
codes given below. Reason: When two pairs of traits are
combined in a hybrid, segregation of
Column-I Column-II one pair of characters is independent of
(A) Linkage (1) Non-parallel
the other pair of characters.
gene
A) Both assertion and reason are true
combination
and the reason is the correct
(B) Recombination (2) Genetic map
(C) Sturtevant (3) Unit of explanation of assertion.
distance B) Both assertion and reason are true
between but the reason is not the correct
genes explanation of assertion.
(D) Centimorgan (4) Physical C) Assertion is true but reason is false.
association D) Both assertion and reason are false.
of genes 87. Assertion: The chromosomal theory of
inheritance was proposed by T. H.
Morgan.
Codes-
Reason: Morgan worked on garden pea
A B C D plants to give this theory.
A) 3 2 4 1 A) Both assertion and reason are true
B) 2 3 1 4 and the reason is the correct
C) 4 1 2 3 explanation of assertion.
D) 1 4 3 2 B) Both assertion and reason are true
84. What map unit (centimorgan) is but the reason is not the correct
adopted in the construction of genetic explanation of assertion.
maps? [NEET–2019] C) Assertion is true but reason is false.
A) A unit distance between two D) Both assertion and reason are false.
expressed genes, representing 10% 88. Assertion: Morgan coined the term
cross over. linkage to describe the physical
B) A unit distance between two association of genes on a chromosome.
expressed genes, representing 100% Reason: Linkage shows more non-
cross over. parental type combination of genes.
C) A unit distance between genes on A) Both assertion and reason are true
chromosomes, representing 1% and the reason is the correct
cross over. explanation of assertion.
D) A unit distance between genes on B) Both assertion and reason are true
chromosomes, representing 50% but the reason is not the correct
cross over. explanation of assertion.
C) Assertion is true but reason is false.
D) Both assertion and reason are false.
Chapter – 5 DPP
101. Among the following, which has a 105. Match the items of Column I with
different mechanism of sex Column II.
determination?
A) Birds
B) Humans Column-I Column-II
C) Drosophila (A) XX-XO (1) Turner’s
D) None of these method of sex syndrome
102. Refer to the given figure which is determination
followed by few statements. Choose (B) XX-XY (2) Female
the incorrect statement about it. method of sex heterogametic
determination
(C) Karyotype-45 (3) Grasshopper
(D) ZW-ZZ (4) Female
method of sex homogametic
determination
108. Assertion: In fruitfly, sex of progeny is 113. The factors that cause mutations are
decided by females. called
Reason: Females produce two types of A) mutagens
gametes. B) teratogens
A) Both assertion and reason are true C) allergens
and the reason is the correct D) none of these
explanation of assertion. 114. An analysis of traits in several of
B) Both assertion and reason are true generations of a family is called
but the reason is not the correct A) mutation
explanation of assertion. B) pedigree analysis
C) Assertion is true but reason is C) genetic map formation
false. D) none of these
D) Both assertion and reason are 115. In a pedigree analysis, the given
false. symbol represents
109. Assertion: Birds show female
heterogamety.
Reason: In birds, the sex of progeny is
determined by males.
A) Both assertion and reason are true
and the reason is the correct A) affected individuals
explanation of assertion. B) mating
B) Both assertion and reason are true C) consanguineous mating
but the reason is not the correct D) unspecified sex
explanation of assertion. 116. Pedigree analysis is used to study the
C) Assertion is true but reason is inheritance pattern of a gene over
false. generations. The character that is
D) Both assertion and reason are studied in the pedigree analysis is
false. equivalent to [NCERT Exemplar]
A) Mendelian trait
Mutation and Genetic Disorders B) Maternal trait
C) Polygamic trait
110. The phenomenon which results in D) Quantitative trait
alteration of DNA sequences is 117. Mendelian disorders are mainly
A) mutation determined by alteration or mutation
B) transpiration in the
C) transcription A) chromosomes
D) translation B) single gene
111. Chromosomal aberrations are C) array of genes
commonly observed in D) none of these
A) cardiac cells 118. Among the following which one is a
B) cancer cells Mendelian disorder?
C) skeletal cells A) Haemophilia
D) none of these B) Sickle cell anaemia
112. A classical example of point mutation C) Cystic fibrosis
is D) All of these
A) gout
B) night blindness
C) sickle cell anaemia
D) Turner’s syndrome
Chapter – 5 DPP
119. Choose the incorrect statement about 124. Haemophilia A and B are due to
Mendelian disorders. deficiencies of respectively clotting
A) These are usually caused by factor
mutation in a single gene. A) VIII and IX
B) These disorders are transmitted to B) IX and VIII
the offspring according to the laws C) VII and IX
of inheritance. D) X and VII
C) Mendelian disorders are always 125. Sickle cell anaemia is a/an
sex linked. A) sex-linked recessive disease
D) The trait in question can be B) sex-linked dominant disease
dominant or recessive. C) autosomal recessive disease
120. A genetic disease transmitted from a D) autosomal dominant disease
carrier female that is phenotypically 126. In sickle cell anaemia, valine replaces
normal to only some male progeny is glutamic acid. This valine is coded by
[NCERT Exemplar] the triplet [NCERT Exemplar]
A) sex-linked dominant A) AAG
B) sex-linked recessive B) GGG
C) autosomal dominant C) GUG
D) autosomal recessive D) GAA
121. Refer to the given pedigree analysis. It 127. Sickle Cell Anaemia (SCA) is
is related to the analysis of transferred from parents to offspring
when
A) father is affected and mother is
normal.
B) father is normal and mother is
carrier.
C) father is normal and mother is
affected.
D) both mother and father are carrier.
128. Match Column-I with Column-II and
choose the correct option from the
A) autosomal dominant trait
codes given below.
B) autosomal recessive trait
C) sex-linked dominant trait Column-I Column-II
D) sex-linked recessive trait (A) Myotonic (1) Autosomal
122. Haemophilia is a/an dystrophy recessive
A) sex-linked recessive disease (B) Sickle cell (2) Sex-linked
B) sex-linked dominant disease anaemia recessive
C) autosomal recessive disease (C) Haemophilia (3) Sex-linked
D) autosomal dominant disease dominant
123. The possibility of a female becoming a (D) Rett (4) Autosomal
haemophilic is syndrome dominant
Codes-
A) extremely high
B) extremely rare A B C D
C) equal to a male (a) 4 1 2 3
D) none of these (b) 4 2 3 1
(c) 3 4 1 2
(d) 2 3 4 1
Chapter – 5 DPP
139. Match Column-I with Column-II and A) formation of abnormal ova in the
choose the correct option from the mother.
codes given below. B) fusion of two ova and one sperm.
C) fusion of two sperms and one
Column-I Column-II ovum.
(A) Aneuploidy (1) An increase in
D) formation of abnormal sperms in
whole set of
the father.
chromosomes
(B) Polyploidy (2) 2n + 1 144. What is the genetic disorder in which
(C) Trisomy (3) Gain or loss of an individual has an overall
a chromosome masculine development,
(D) Monosomy (4) 2n − 1 gynaecomastia and is sterile? [NEET-
2019]
Codes- A) Turner’s syndrome
B) Klinefelter’s syndrome
A B C D C) Edward’s syndrome
A) 1 3 4 2 D) Down’s syndrome
B) 3 1 2 4 145. In which genetic condition, each cell
C) 4 2 3 1 in the affected person, has three sex
D) 2 4 1 3
chromosomes XXY? [NEET Odisha-
140. A disease caused by an autosomal
2019]
primary nondisjunction is [NEET-
A) Turner’s syndrome
2017]
B) Thalassemia
A) Klinefelter’s syndrome
C) Kleinfelter’s syndrome
B) Turner’s syndrome
D) Phenylketonuria
C) Sickle cell anaemia
146. A disorder caused due to the absence
D) Down’s syndrome
of one of the X chromosomes is
141. Refer to the given figure. It is showing
A) Turner’s syndrome
the characteristic features of
B) Down’s syndrome
C) Klinefelter’s syndrome
D) Edward’s syndrome
147. Assertion: The possibility of a female
becoming a haemophilic is extremely
rare.
Reason: For being haemophilic, the
mother of such a female has to be at
least carrier and the father should be
A) Down’s syndrome haemophilic.
B) Turner’s syndrome A) Both assertion and reason are true
C) Klinefelter’s syndrome and the reason is the correct
D) None of these explanation of assertion.
142. The disease caused by the trisomy of B) Both assertion and reason are true
chromosome number 21 is but the reason is not the correct
A) Turner’s syndrome explanation of assertion.
B) Haemophilia C) Assertion is true but reason is
C) Klinefelter’s syndrome false.
D) Down’s syndrome D) Both assertion and reason are
143. An abnormal human baby with ‘XXX’ false.
sex chromosomes was born due to
[AIPMT-2015]
Chapter – 5 DPP
ANSWER KEY
PRINCIPLE OF INHERITANCE AND VARIATION
Q 01 02 03 04 05 06 07 08 09 10
Ans D B A D D A C B C B
Q 11 12 13 14 15 16 17 18 19 20
Ans D D A A D C D B C B
Q 21 22 23 24 25 26 27 28 29 30
Ans D A B B C B A C B A
Q 31 32 33 34 35 36 37 38 39 40
Ans C A B D B A B D B B
Q 41 42 43 44 45 46 47 48 49 50
Ans A D B D C D C C B D
Q 51 52 53 54 55 56 57 58 59 60
Ans B B B B A C B D C C
Q 61 62 63 64 65 66 67 68 69 70
Ans B C A B C B D D C B
Q 71 72 73 74 75 76 77 78 79 80
Ans D D D D D A B A C B
Q 81 82 83 84 85 86 87 88 89 90
Ans C A C C C B D C C A
Q 91 92 93 94 95 96 97 98 99 100
Ans B B D C A D C D B C
Q 101 102 103 104 105 106 107 108 109 110
Ans A A B B D C A D C A
Q 111 112 113 114 115 116 117 118 119 120
Ans B C A B C A B D C D
Q 121 122 123 124 125 126 127 128 129 130
Ans A A B A C C D A B A
Q 131 132 133 134 135 136 137 138 139 140
Ans A B C D B C A A B D
Q 141 142 143 144 145 146 147 148 149
Ans A D A B C A A C B