NEET Exam  >  NEET Tests  >  Biology Class 12  >  Multiple Choice Questions (MCQs): Inheritance & Variation - NEET MCQ

Multiple Choice Questions (MCQs): Inheritance & Variation - NEET MCQ


Test Description

25 Questions MCQ Test Biology Class 12 - Multiple Choice Questions (MCQs): Inheritance & Variation

Multiple Choice Questions (MCQs): Inheritance & Variation for NEET 2024 is part of Biology Class 12 preparation. The Multiple Choice Questions (MCQs): Inheritance & Variation questions and answers have been prepared according to the NEET exam syllabus.The Multiple Choice Questions (MCQs): Inheritance & Variation MCQs are made for NEET 2024 Exam. Find important definitions, questions, notes, meanings, examples, exercises, MCQs and online tests for Multiple Choice Questions (MCQs): Inheritance & Variation below.
Solutions of Multiple Choice Questions (MCQs): Inheritance & Variation questions in English are available as part of our Biology Class 12 for NEET & Multiple Choice Questions (MCQs): Inheritance & Variation solutions in Hindi for Biology Class 12 course. Download more important topics, notes, lectures and mock test series for NEET Exam by signing up for free. Attempt Multiple Choice Questions (MCQs): Inheritance & Variation | 25 questions in 25 minutes | Mock test for NEET preparation | Free important questions MCQ to study Biology Class 12 for NEET Exam | Download free PDF with solutions
Multiple Choice Questions (MCQs): Inheritance & Variation - Question 1

In a plant, red fruit (R) is dominant over yellow fruit (r) and tallness (T) is dominant over shortness (t). If a plant with RRTt genotype is crossed with a plant that is rrtt:

Detailed Solution for Multiple Choice Questions (MCQs): Inheritance & Variation - Question 1

If a plant with RRTt genotype is crossed with a plant that is rrtt 50% of the offspring will be tall with red fruit.

Multiple Choice Questions (MCQs): Inheritance & Variation - Question 2

What will be expected blood groups in the off spring when there is a cross between AB blood group mother and heterozygous B blood group father?

Detailed Solution for Multiple Choice Questions (MCQs): Inheritance & Variation - Question 2

AB blood group of mother have two alleles IA and IB. The heterozygous B blood group of father has alleles IB and i. The possible outcome are IA IB,IAi,IBIB and IBi. That form AB, A, B and B blood group respectively.

1 Crore+ students have signed up on EduRev. Have you? Download the App
Multiple Choice Questions (MCQs): Inheritance & Variation - Question 3

Which of the following amino acid substitutions in the beta chain of the haemoglobin molecule leads to the development of sickle cell anaemia?

Detailed Solution for Multiple Choice Questions (MCQs): Inheritance & Variation - Question 3
In sickle cell anemia, glutamic acid is substituted by valine in the beta chain of hemoglobin.
Multiple Choice Questions (MCQs): Inheritance & Variation - Question 4

Two genes p and q showing 1.3% of recombination while other two genes x and y show 37.2 percent of recombination. Which pair of genes is close to each other?

Detailed Solution for Multiple Choice Questions (MCQs): Inheritance & Variation - Question 4

Two genes p and q showing 1.3% of recombination while other two genes x and y show 37.2 percent of recombination. p and q genes are present close to each other as they show less recombination percentage.

Multiple Choice Questions (MCQs): Inheritance & Variation - Question 5

Assertion: An organism with lethal mutation may not even develop beyond the zygote stage.

Reason: All types of gene mutations are lethal.

Detailed Solution for Multiple Choice Questions (MCQs): Inheritance & Variation - Question 5

An organism with lethal mutation may not even develop beyond zygote stage due to change in gene but all kinds of mutations are not lethal. Mutation is main source of variation essential for evolution.

Multiple Choice Questions (MCQs): Inheritance & Variation - Question 6
Match the following:

Column I
i. Down’s syndrome
ii. Klinefelter’s syndrome
iii. Turner’s syndrome

Column II
a. Broad palm with characteristic palm crease
b. Gynaecomastia
c. Rudimentary ovaries
d. XO
e. XXY
f. Physical development is retarded.
Detailed Solution for Multiple Choice Questions (MCQs): Inheritance & Variation - Question 6
Down’s syndrome is characterized by physical development that is retarded and has a broad palm with a characteristic palm crease (i-a). It is caused by an extra chromosome 21 (i-c).
Klinefelter’s syndrome involves having an extra X chromosome, making the karyotype XXY, and is associated with features such as gynaecomastia and delayed physical development (ii-b,e,f).
Turner’s syndrome involves a missing X chromosome, making the karyotype XO, and is associated with rudimentary ovaries and a broad palm with a characteristic palm crease (iii-c,d).
Multiple Choice Questions (MCQs): Inheritance & Variation - Question 7
The genes which are involved in alpha Thalassemia are---- and ----- while in beta thalassemia are----.
Detailed Solution for Multiple Choice Questions (MCQs): Inheritance & Variation - Question 7
Alpha Thalassemia involves genes HBA1 and HBA2 (located on chromosome 16).
Beta Thalassemia involves the HBB gene (located on chromosome 11).
Multiple Choice Questions (MCQs): Inheritance & Variation - Question 8
A cell at the telophase stage is observed by a student in a plant brought from the field. He tells his teacher that this cell is not like other cells at the telophase stage. There is no formation of a cell plate and thus the cell is containing more chromosomes as compared to other dividing cells. This would result in:
Detailed Solution for Multiple Choice Questions (MCQs): Inheritance & Variation - Question 8
The absence of a cell plate and the presence of more chromosomes suggest aneuploidy, where the cell has an abnormal number of chromosomes due to errors in chromosome segregation. Polyploidy involves the entire set of chromosomes, while polyteny refers to chromosome duplication without cell division.
Multiple Choice Questions (MCQs): Inheritance & Variation - Question 9

F2 generation in a Mendelian cross showed that both genotypic and phenotypic ratios are same as 1 : 2 : 1. It represents in case of

Detailed Solution for Multiple Choice Questions (MCQs): Inheritance & Variation - Question 9

Monohybrid cross with incomplete dominance shows both genotypic and phenotypic ratio as same (1 : 2 : 1).

Genotypic ratio - 1(AA):2(Aa):1(aa)
Phenotypic ratio - 1(Red):2(Pink):1(White)

Multiple Choice Questions (MCQs): Inheritance & Variation - Question 10

In Mendel's experiments with garden pea, round seed shape (RR) was dominant over Wrinkled Seeds (rr), Yellow cotyledon (YY) was dominant over green cotyledon (yy). What are the expected Phenotypes in the F2 generation of the cross RRYY x rryy?

Detailed Solution for Multiple Choice Questions (MCQs): Inheritance & Variation - Question 10

The expected Phenotypes in the F2 generation of the cross RRYY x rryy is Round-yellow; wrinkled-yellow; round-green and wrinkled-green in 9:3:3:1 similar to dihybrid results.

Multiple Choice Questions (MCQs): Inheritance & Variation - Question 11

Which organism’s male contain a pair of Z chromosome as sex chromosome besides autosomes?

Detailed Solution for Multiple Choice Questions (MCQs): Inheritance & Variation - Question 11

In birds male contain a pair of Z chromosome as sex chromosome besides autosomes while female contain one Z and one W chromosome.

Multiple Choice Questions (MCQs): Inheritance & Variation - Question 12

Crossing over occurs at:

Detailed Solution for Multiple Choice Questions (MCQs): Inheritance & Variation - Question 12

Crossing over occurs at four strand stage of panchytene of meiosis-I. Each homologous chromosome has two stands. Exchange of gene occurs during this period.

Multiple Choice Questions (MCQs): Inheritance & Variation - Question 13

Deviation from Medelism’s occurs due to
a. Multiple alleles
b. Co dominance
c. Linkage and crossing over
d. Independent assortment

Detailed Solution for Multiple Choice Questions (MCQs): Inheritance & Variation - Question 13

Deviation from Medelism’s occurs due to co-dominance, multiple alleles, incomplete dominance in which single gene is not completely dominant over the other to produce dominant trait.

Multiple Choice Questions (MCQs): Inheritance & Variation - Question 14

Find the correct match:

Detailed Solution for Multiple Choice Questions (MCQs): Inheritance & Variation - Question 14

Thalassemia can be classified according to which chain of the haemoglobin molecule is affected. In α Thalassemia, production of α globin chain is affected while in β Thalassemia, production of β globin chain is affected. α Thalassemia is controlled by two closely linked genes HBA1 and HBA2 on chromosome 16 of each parent and it is observed due to mutation or deletion of one or more of the four genes. The more genes affected, the less alpha globin molecules produced. While β Thalassemia is controlled by a single gene HBB on chromosome 11 of each parent and occurs due to mutation of one or both the genes.

Multiple Choice Questions (MCQs): Inheritance & Variation - Question 15

Chromosome theory of XY sex determination was proposed by:

Detailed Solution for Multiple Choice Questions (MCQs): Inheritance & Variation - Question 15

Chromosome theory of XY sex determination was proposed by Wilson and Stevens.

Multiple Choice Questions (MCQs): Inheritance & Variation - Question 16

The crossing of F1 to any one of the parents is called?

Detailed Solution for Multiple Choice Questions (MCQs): Inheritance & Variation - Question 16

The crossing of F1 to any one of the parents is called back cross. It is used to check the purity of individual. When F1 is crossed with recessive parent, it is called test cross.

Multiple Choice Questions (MCQs): Inheritance & Variation - Question 17
Which of the following statements are correct?

(i) Polyploidy is caused due to failure of cytokinesis after telophase.
(ii) Polyploidy results in an increase in the number of autosomes.
(iii) Turner’s syndrome is an example of polyploidy.
(iv) Polyploidy results in an increase in a whole set of chromosomes.
Detailed Solution for Multiple Choice Questions (MCQs): Inheritance & Variation - Question 17
Polyploidy involves an increase in a whole set of chromosomes, not just autosomes (iv).
It is indeed caused by the failure of cytokinesis, resulting in cells with multiple sets of chromosomes (i).
Turner’s syndrome is not an example of polyploidy; it is a monosomy (iii).
Multiple Choice Questions (MCQs): Inheritance & Variation - Question 18

Which of the following would not be a feature seen in a patient with the following karyotype?

Detailed Solution for Multiple Choice Questions (MCQs): Inheritance & Variation - Question 18

A patient with Down’s syndrome (karyotype 47,XX,+21) might exhibit features such as many loops on fingertips, congenital heart disease, and a big and wrinkled tongue. Mucus clogging of airways is not typically associated with Down’s syndrome.

Multiple Choice Questions (MCQs): Inheritance & Variation - Question 19

Assertion: In human beings, 23 pairs of chromosomes are present in diploid cells.

Reason: 22 pairs of chromosomes are equal in male and female but a pair sex chromosome is different in them.

Detailed Solution for Multiple Choice Questions (MCQs): Inheritance & Variation - Question 19

In human beings, 23 pairs of chromosomes are present in diploid cells.
Twenty two pairs of chromosomes are equal in male and female but a pair sex chromosome is different in them. Male contain XY and female contain XX sex chromosome.

Multiple Choice Questions (MCQs): Inheritance & Variation - Question 20

Linkage is the_________.

Detailed Solution for Multiple Choice Questions (MCQs): Inheritance & Variation - Question 20

Linkage is the physical association of two genes present on same chromosome. Genes located close to each other have high linkage percentage.

Multiple Choice Questions (MCQs): Inheritance & Variation - Question 21
Match the following:

Column I
a. Phenylketonuria
b. Down's syndrome
c. Klinefelter's syndrome
d. Turner's syndrome

Column II
i. Autosomal trisomy associated with mongolism
ii. Gynaecomastia
iii. Autosomal recessive trait associated with mental retardation
iv. Sterile females with rudimentary ovaries
Detailed Solution for Multiple Choice Questions (MCQs): Inheritance & Variation - Question 21
Phenylketonuria is an autosomal recessive trait associated with mental retardation (a-iii).
Down's syndrome is an autosomal trisomy associated with mongolism (b-i).
Klinefelter's syndrome is characterized by gynaecomastia (c-ii) and involves sterile males with rudimentary testes.
Turner's syndrome involves sterile females with rudimentary ovaries (d-iv).
Multiple Choice Questions (MCQs): Inheritance & Variation - Question 22

If two pea plants having red (dominant) coloured flowers with unknown genotypes are crossed, 75% of the flowers are red and 25% are white. The genotypic constitution of the parents having red coloured flowers will be

Detailed Solution for Multiple Choice Questions (MCQs): Inheritance & Variation - Question 22

When two pea plants having red (dominant)c coloured flowers with unknown genotype are crossed, the 75% red and 25% white flowered plants will be produced by following the law of Mendel. This is possible only if the parents are heterozygotes. 

Multiple Choice Questions (MCQs): Inheritance & Variation - Question 23

Which of the following statements is true regarding the “law of independent assortment”?

Detailed Solution for Multiple Choice Questions (MCQs): Inheritance & Variation - Question 23

Independent Assortment describes how different genes independently separate from one another when reproductive cells develop. Independent assortment of genes and their corresponding traits was first observed by Gregor Mendel. Recombination occurs during meiosis and is a process that breaks and recombines pieces of DNA to produce new  combinations of genes. Recombination scrambles pieces of maternal and paternal genes, which ensures that genes assort independently from one another.

Multiple Choice Questions (MCQs): Inheritance & Variation - Question 24

On the basis of sex chromosome shown below, the bird shown is:

Detailed Solution for Multiple Choice Questions (MCQs): Inheritance & Variation - Question 24

Male birds bears ZZ sex chromosome as sex determination is ZO type, in which ZZ is male and ZO is female.

Multiple Choice Questions (MCQs): Inheritance & Variation - Question 25

In a given plant, red colour (R) of fruits is dominant over white fruit (r): and tallness (T) is dominant over dwarfness (t). If a plant with genotype RRTt is crossed with a plant of genotype rrtt, what will be the percentage of tall plants with red fruits in the next generation?

Detailed Solution for Multiple Choice Questions (MCQs): Inheritance & Variation - Question 25

According to question, tallness (T) is dominant over dwarfism (t) and red colour (R) is dominant over white (r) fruit colour.

Parent Generation; P1 : RRTt  x  rrtt

F1 generation :

Phenotypic ratio = 1  (tall plant, red fruit)         
: 1 (dwarf plant, red fruit)
; thus, percent of tall plant with red fruit is 50%.

122 videos|311 docs|196 tests
Information about Multiple Choice Questions (MCQs): Inheritance & Variation Page
In this test you can find the Exam questions for Multiple Choice Questions (MCQs): Inheritance & Variation solved & explained in the simplest way possible. Besides giving Questions and answers for Multiple Choice Questions (MCQs): Inheritance & Variation, EduRev gives you an ample number of Online tests for practice

Top Courses for NEET

122 videos|311 docs|196 tests
Download as PDF

Top Courses for NEET