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THE TOPPERS ACADEMY FAIZ M ROAD QUETTA

Humans have X – linked recessive traits Q.8 Genes form ________ on ________ of
like: homologous chromosomes.
A) Hemophilia A) Pairs, Pairs C) Tetrads, pairs
B) Vitamin D – resistant rickets B) Pairs, tetrads D) Tetrads, tetrads
C) Hypophosphatemic rickets Q.9 When an effect caused by a gene or
D) SRY gene gene pair at one locus interferes with or
Q.2 Many X – linked traits in man are also hides the effect caused by another gene or
found X – linked in other mammals like: gene pair at another locus, such
A) Mouse and rabbit phenomenon of gene interaction is called:
B) Dog and Sheep A) Epistasis C) Over dominance
C) Donkey and horse B) Pleiotropy D) Co dominance
D) Mouse, rabbit, dog, sheep, donkey, Q.10 ABO locus is on chromosome
cattle, kangaroo and chimpanzee all number:
Q.3 Gene is a basic unit of: A) 19 C) 11
A) Inheritance C) Excretion B) 9 D) 21
B) Coordination D) Respiration Q.11 The epistatic gene H changes a
Q.4 Genes are actually parts of _____ precursor substance into substance:
comprising its base sequence: A) H C) A
A) Chromosome C) RNA B) D D) B
B) DNA D) Chromatid Q.12 Substance H produces an enzyme that
Q.5 ________ are responsible for producing inserts sugar into a precursor ______
startling inherited resemblances as well on the surface of RBC:
as distinctive variations among A) Lipoprotein C) Glycoprotein
generations. B) Nucleoprotein D) Glycolipids
A) Chromosomes C) Genomes Q.13 Insertion of antigen A and B on the
B) Genes D) Nucleic acids surface of RBC depends upon the
Q.6 When genes pass in the form of product of gene:
intact parental combination between A) H C) IB
generations: B) IA D) IA or IB
A) Inherited similarities are conserved Q.14 A person with Bombay phenotype
B) Non-inherited similarities are conserved lacks:
C) Variations energy A) Antigen A and B in blood
D) Non-inherited variations emerge B) Antigen A and B in body
Q.7 When genes shuffle, mutate or juggle C) Antigen A and B on RBC
with each other: D) Antigen A and B in lymph
A) Genetic continuity is conserved Q.15 Pick up the one which illustrate
B) Inherited variations are conserved Bombay
C) Variations occur phenotype:
D) Inherited similarities are conserved A) IAIA, HH C) IAIB, hh
B) IAIB, Hh D) ii, HH
Q.16 A phenomenon of gene interaction in
which a gene interferes in the effect of
another gene is called:

LEC. Zirak Nawaz (M. Phil Zoology) 03128130591


THE TOPPERS ACADEMY FAIZ M ROAD QUETTA
A) Pleiotropy C) Over dominance A) IA C) IA and IB both
B) Epistasis D) Co dominance B) IB D) D
Q.17 Epistasis is an interaction between: Q.25 Pick up the genotype which produces
A) Different alleles of the same gene phenotype A:
B) Different genes occupying different loci A) IAIA C) IAIA or IAi
C) Same gene of the different loci B) IAi D) ii
D) Different genes occupying same locus Q.26 The homozygous “ii” will produce
Q.18 Bombay phenotype is an example of: phenotype:
A) Dominance C) Epistasis A) A C) AB
B) Pleiotropy D) Gene linkage B) B D) O
Q.19 The cells of _______ contains an Q.27 The blood group alleles start their
enormous amount of DNA. expression at early embryonic stage
A) Prokaryotes C) Eukaryotes and keep on expressing themselves till:
B) Protists D) Fungi A) Puberty C) Death
Q.20 The mutation in _______ have little B) Old stage D) Eighties
evolutionary consequence than germ Q.28 The blood serum of A phenotype
line changes. contains:
A) Sex cells A) Anti – A antibodies
B) Gametes B) No antibodies
C) Gamete mother cells C) Anti – B antibodies
D) Somatic cells D) Both antibodies
Q.21 The mutation in ________ is passed to Q.29 B phenotype of blood contains:
subsequent generations thus providing A) Anti – A antibodies
the raw material from which natural B) Anti – B antibodies
selection produces evolutionary changes. C) Anti A and Anti B antibodies
A) Somatic cells D) No antibody
B) Non – reproductive cells Q.30 Blood phenotype AB have:
C) Germ line cells A) Anti – A antibodies
D) Skin cells B) Anti – B antibodies
Q.22 Mutations can broadly be classified C) Both Anti A and B antibodies
as: D) Neither anti – A nor Anti – B antibodies
A) Chromosomal aberration of number Q.31 Any blood transfusion is ideally safe
and structure if it:
B) Point mutation and gene mutation A) Does not cause agglutination in the
C) Chromosomal aberration of number recipient
and point mutation B) Cause agglutination in the recipient
D) Chromosomal aberration and point C) Does not cause agglutination in the
mutation donor
Q.23 Allele IA specifies production of D) Cause agglutination in the donor
antibodies: Q.32 Agglutination of blood leads to serious
A) Against A C) Against A and B results because clumped blood cells
B) Against B D) Against O cannot:
Q.24 Allele i is recessive to: A) Carry O2

LEC. Zirak Nawaz (M. Phil Zoology) 03128130591


THE TOPPERS ACADEMY FAIZ M ROAD QUETTA
B) Pass through fine capillaries C) Chromosomal aberrations
C) Carry CO2 D) Point mutations
D) Carry food and wastes Q.40 Modern industrial societies are
Q.33 Before giving transfusion the blood exposed
samples of the donor and the recipient to point mutations mainly by:
are: A) Mutagenic radiations
A) Screened for compatibility B) Spontaneous pairing errors
B) Cross matched for compatibility C) Chemical mutagens
C) Filtered for compatibility D) Non-disjunction
D) Centrifuged for compatibility Q.41 Sickle cell anemia and phenyl
Q.34 If incompatible blood is transfused, ketonuria
the RBCs of the: are well known examples of:
A) Recipient are destroyed A) Point mutations
B) Either recipient or donor or both are B) Chromosomal aberrations
destroyed C) Chromosomal mutations
C) Donor are destroyed D) Non-disjunctions
D) No body are destroyed Q.42 In sickle cell anemia a point mutations
Q.35 Blood group A can be transfused only leads to the change of ________ at
into: position 6 from N terminal end in
A) A recipient hemoglobin β chain.
B) B recipient A) Glutamic acid into serine
C) AB recipient B) Serine into glutamic acid
D) A and AB recipient C) Glutamic acid into valine
Q.36 AB blood can be transfused only into: D) Valine into glutamic acid
A) B recipient Q.43 Sickle cell hemoglobin have reduced
B) A recipient ability to:
C) AB recipient A) Carry CO2 C) Release O2
D) B and AB recipient B) Carry O2 D) Release CO2
Q.37 ABO blood system is encoded by a Q.44 Humans have:
single: A) 46 chromosomes
A) Polymorphic gene B) 46 pairs of chromosomes
B) Homomorphic gene C) 23 chromosomes
C) Isomorphic gene D) 22pairs of chromosomes
D) Amorphic gene Q.45 In humans division of chromosomes is
Q.38 The gene I at chromosome # 9 of as under:
human population have: A) 23 autosome, one pair of sex
A) Two alleles C) Four alleles chromosomes
B) Three alleles D) Five alleles B) 22 autosome, one pair of sex
Q.39 If the alterations involve only one or a chromosomes
few base pairs in the coding sequence C) 23 pairs of autosome, one pair of sex
they are called: chromosomes
A) Chromosomal mutations D) 22 pairs of autosome, one pair of sex
B) Mega changes chromosomes

LEC. Zirak Nawaz (M. Phil Zoology) 03128130591


THE TOPPERS ACADEMY FAIZ M ROAD QUETTA
B) Male
Q.46 The human female differs from C) Abnormal male
human male in having: D) Abnormal female
A) X chromosome Q.54 All sixty four codons were tested by
B) Two X chromosomes making artificial mRNA and triplet
C) Y chromosome codons by:
D) XY chromosomes A) Nierenberg
Q.47 Human female differs from human B) Leader
male in having: C) Khorana
A) 22 homologous pairs of chromosomes D) Nierenberg, Leader and Khorana
B) 22 homologous pairs of autosomes Q.55 Many different alleles of a gene may
C) 23 homologous pairs of chromosomes be produced by:
D) One pair of sex chromosomes A) Evolution C) Reshuffling
Q.48 Human male differs from human B) Mutation D) Crossing over
female in having: Q.56 All such altered, alternative forms of a
A) One non-homologous pairs of gene, whose number is more than two,
chromosomes are called:
B) 23 non-homologous pairs of A) Allelomorphs C) Multiple alleles
chromosomes B) Fixed alleles D) Pseudo alleles
C) 22 homologous pairs of chromosome Q.57 ABO blood system have:
D) 23 homologous pairs of chromosome A) Two different phenotypes
Q.49 The male determining gene of the Y – B) Four different phenotypes
chromosome is called: C) Three different phenotypes
A) tfm C) SDRY D) Five different phenotypes
B) SRY D) TSDRY Q.58 A person having antigen A on the
Q.50 It is essential for triggering the surface of RBC, has:
development of maleness in humans: A) Antibodies against A
A) Presence of Y chromosome B) Antibodies against O
B) Presence of SRY gene on Y chromosome C) Antibodies against B
C) X – Y balance D) Antibodies against A and B
D) Autosome and X chromosome balance Q.59 A person having neither antigen A
In humans: nor B have:
A) Same type of gametes are produced A) No antibodies
B) Same type of sperms are produced B) Antibodies against B
C) Same type of eggs are produced C) Antibodies against A
D) Different type of eggs are produced D) Antibodies against A and B both
Q.52 In humans, the chances of male and Q.60 In phenylketonuria:
female offspring are theoretically: A) Phenylalanine hydroxylase is not formed
A) 1:2:1 C) 1:1 B) Phenylalanine hydroxylase is not
B) 2:1 D) 3:1 degraded
Q.53 In humans, if X-carrying sperm C) Phenylalanine is not formed
fertilizes the egg, the offspring will be: D) Adenosine deaminase is not formed
A) Female

LEC. Zirak Nawaz (M. Phil Zoology) 03128130591

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