Genetics and Evolution
18 lessons
Topic index in NCERT order
18 of 18 lessons by the NCERT chapter they teach from, in book order. The page is the first printed page of your NCERT book the lesson cites; PYQs are the past NEET questions on that topic.
Class 12 Biology, Chapter 4: Principles of Inheritance and Variation
- Mendel Inheritancep. 598 PYQs
- Incomplete Dominance Codominancep. 606 PYQs
- Linkage Recombination Mappingp. 673 PYQs
- Sex Determination Linkagep. 712 PYQs
- Mendelian Disorders Pedigreep. 724 PYQs
- Mutations Genetic Disordersp. 735 PYQs
Class 12 Biology, Chapter 5: Molecular Basis of Inheritance
- DNA RNA Structurep. 811 PYQ
- Genetic Material DNA Packagingp. 839 PYQs
- DNA Replicationp. 894 PYQs
- Genetic Codep. 951 PYQ
- Transcription Translationp. 9515 PYQs
- Gene Regulation Lac Operonp. 1004 PYQs
- Human Genome Projectp. 1024 PYQs
Class 12 Biology, Chapter 6: Evolution
- Origin Life Panspermiap. 1110 PYQs
- Evidences Evolutionp. 1138 PYQs
- Hardy Weinberg Principlep. 1212 PYQs
- Natural Selection Driftp. 1214 PYQs
- Hominid Evolutionp. 1242 PYQs
DNA Replication
DNA RNA Structure
Evidences Evolution
Gene Regulation Lac Operon
Genetic Code
Genetic Material DNA Packaging
Hardy Weinberg Principle
Hominid Evolution
Human Genome Project
Incomplete Dominance Codominance
Linkage Recombination Mapping
Mendel Inheritance
Mendelian Disorders Pedigree
Mutations Genetic Disorders
Natural Selection Drift
Origin Life Panspermia
Sex Determination Linkage
Transcription Translation
NCERT lines NEET tested in this unit
Each line with its printed NCERT page and the past NEET questions that tested it.
Past-paper questions from this unit
82 questions from NEET 2020, 2021, 2022, 2023, 2024, 2025, 2026. Answers verified against NTA official keys.
By year in our set: 2020 (6) · 2021 (11) · 2022 (14) · 2023 (12) · 2024 (15) · 2025 (13) · 2026 (11)
Lesson: Mutations Genetic Disorders
Lesson: Natural Selection Drift
Lesson: Hardy Weinberg Principle
Lesson: Gene Regulation Lac Operon
Which of the following statements about lac-operon is correct ?
Lesson: Evidences Evolution
Which of the following is not evidence for evolution ?
Lesson: Hominid Evolution
Lesson: Evidences Evolution
Lesson: Transcription Translation
Which of the following enzymes synthesizes precursor mRNA ?
Lesson: Incomplete Dominance Codominance
Lesson: Evidences Evolution
Lesson: Mendel Inheritance
Lesson: Mendel Inheritance
Lesson: Mendelian Disorders Pedigree
Lesson: Genetic Code
Who proposed that the genetic code for amino acids should be made up of three nucleotides?
Lesson: Evidences Evolution
Lesson: Genetic Material DNA Packaging
Lesson: Transcription Translation
Which factor is important for termination of transcription?
Lesson: Sex Determination Linkage
Lesson: Genetic Material DNA Packaging
Lesson: Transcription Translation
Lesson: Incomplete Dominance Codominance
What is the pattern of inheritance for polygenic trait?
Lesson: Transcription Translation
Lesson: Genetic Material DNA Packaging
Lesson: Human Genome Project
Which chromosome in the human genome has the highest number of genes?
Lesson: Gene Regulation Lac Operon
The lactose present in the growth medium of bacteria is transported to the cell by the action of
Lesson: Mendel Inheritance
Lesson: Incomplete Dominance Codominance
Lesson: Transcription Translation
Lesson: Mendel Inheritance
Lesson: Mendel Inheritance
Lesson: DNA Replication
Which of the following statement is correct regarding the process of replication in E.coli?
Lesson: Genetic Material DNA Packaging
Lesson: Evidences Evolution
The flippers of the Penguins and Dolphins are the example of the
Lesson: Hominid Evolution
Lesson: Hardy Weinberg Principle
Which one of the following factors will not affect the Hardy-Weinberg equilibrium?
Lesson: Mutations Genetic Disorders
Lesson: Transcription Translation
Lesson: Transcription Translation
Lesson: Incomplete Dominance Codominance
Lesson: Incomplete Dominance Codominance
The phenomenon of pleiotropism refers to
Lesson: Transcription Translation
What is the role of RNA polymerase III in the process of transcription in Eukaryotes?
Lesson: DNA Replication
Among eukaryotes, replication of DNA takes place in :
Lesson: Human Genome Project
Expressed Sequence Tags (ESTs) refers to
Lesson: Linkage Recombination Mapping
Lesson: Genetic Material DNA Packaging
Unequivocal proof that DNA is the genetic material was first proposed by
Lesson: Mutations Genetic Disorders
Lesson: Genetic Material DNA Packaging
Lesson: Mutations Genetic Disorders
Broad palm with single palm crease is visible in a person suffering from-
Lesson: Gene Regulation Lac Operon
Lesson: Evidences Evolution
Select the correct group/set of Australian Marsupials exhibiting adaptive radiation.
Lesson: Transcription Translation
Lesson: Genetic Material DNA Packaging
Lesson: Sex Determination Linkage
XO type of sex determination can be found in :
Lesson: Transcription Translation
The process of translation of mRNA to proteins begins as soon as :
Lesson: Mendel Inheritance
Lesson: Mendelian Disorders Pedigree
Which of the following occurs due to the presence of autosome linked dominant trait ?
Lesson: Human Genome Project
Lesson: Linkage Recombination Mapping
Lesson: Gene Regulation Lac Operon
Lesson: Natural Selection Drift
Lesson: Genetic Material DNA Packaging
If the length of a DNA molecule is 1.1 metres, what will be the approximate number of base pairs?
Lesson: Linkage Recombination Mapping
Lesson: Mendelian Disorders Pedigree
Lesson: DNA Replication
Lesson: Evidences Evolution
Which of the following statements is not true?
Lesson: Mendel Inheritance
Lesson: Natural Selection Drift
The factor that leads to Founder effect in a population is :
Lesson: DNA Replication
Match List-I with List-II. Choose the correct answer from the options given below. (a) (b) (c) (d)
Lesson: Mutations Genetic Disorders
Mutations in plant cells can be induced by:
Lesson: Transcription Translation
What is the role of RNA polymerase III in the process of transcription in eukaryotes?
Lesson: Human Genome Project
Lesson: Transcription Translation
Identify the correct statement.
Lesson: DNA RNA Structure
Lesson: Transcription Translation
Which of the following RNAs is not required for the synthesis of protein?
Lesson: Mendelian Disorders Pedigree
Lesson: Evidences Evolution
Lesson: Natural Selection Drift
Lesson: Genetic Material DNA Packaging
Lesson: Transcription Translation
Name the enzyme that facilitates opening of DNA helix during transcription.
Lesson: Incomplete Dominance Codominance
Identify the wrong statement with reference to the gene ‘I’ that controls ABO blood groups.
Lesson: Transcription Translation
The first phase of translation is :
Lesson: Mendel Inheritance
Exam traps and common mistakes in this unit
Lesson: DNA Replication
Category: Sign Convention
DNA polymerase synthesises only 5'→3'. Leading strand: continuous, same direction as fork. Lagging: discontinuous (Okazaki), opposite to fork.
When it triggers
Question on Okazaki, leading vs lagging, primer direction.
How to avoid
Reading template 3'→5'; synthesising 5'→3'. Lagging strand needs short fragments because it can't run continuously against fork direction.
Lesson: Genetic Code
Category: Overthinking
Students misstate that all 64 codons code for amino acids, forgetting 3 are stop codons, or forget AUG's dual role.
When it triggers
A question asks how many codons code for amino acids and offers 64 as a distractor instead of 61, or asks what AUG codes for and omits its role as the initiator codon.
How to avoid
Of 64 possible triplet codons, 61 code for amino acids and 3 (UAA, UAG, UGA) are stop/terminator codons that code for no amino acid; AUG both codes for Methionine and acts as the initiator codon.
Lesson: Genetic Code
Category: Inorganic Exception
Students assume any insertion/deletion causes a frameshift, missing that insertions/deletions of three bases (or multiples of three) leave the reading frame unaltered.
When it triggers
A question states 3 bases (or a multiple of 3) were inserted or deleted and asks whether the reading frame shifts, and a distractor claims a frameshift always occurs.
How to avoid
Insertion or deletion of one or two bases shifts the reading frame from that point (frameshift mutation); insertion or deletion of three bases, or a multiple of three, only adds/removes whole codons (amino acids) and the reading frame remains unaltered thereafter, as shown by the 'RAM HAS RED CAP' example.
Lesson: Genetic Material DNA Packaging
Category: Similar Terms
NEET questions swap which experiment proved DNA is the genetic material versus which only showed a 'transforming principle' existed.
When it triggers
A question describes the heat-killed S + live R mouse experiment and asks who proved DNA is the genetic material, expecting Griffith when it was Avery-MacLeod-McCarty (biochemical proof) or Hershey-Chase (unequivocal proof with bacteriophages).
How to avoid
Griffith (1928) only showed a 'transforming principle' existed without identifying its biochemical nature; Avery-MacLeod-McCarty (1933-44) showed DNA alone causes transformation; Hershey-Chase (1952) gave the unequivocal proof using radiolabeled phosphorus/sulfur in bacteriophages.
Lesson: Genetic Material DNA Packaging
Category: Negative Marking
Students confuse the number of DNA base pairs per nucleosome (200 bp) with the number of histone molecules per octamer (8).
When it triggers
A question asks 'how many base pairs are wrapped in a typical nucleosome' and offers 8 as a distractor, or asks the number of histone molecules and offers 200.
How to avoid
A histone octamer is made of eight histone molecules; a typical nucleosome (DNA wrapped around that octamer) contains 200 bp of DNA helix — these are two distinct numbers from the same sentence.
Lesson: Hardy Weinberg Principle
Category: Negative Marking
Five forces disturb HW: mutation, gene flow, drift, selection, non-random mating. ANY of these violates equilibrium.
When it triggers
Question asks which factor maintains/disturbs HW.
How to avoid
Random mating + no other forces → equilibrium. ANY of mutation/migration/drift/selection/assortative mating → disequilibrium.
Lesson: Mendel Inheritance
Category: Similar Terms
Monohybrid: genotype 1:2:1 (AA:Aa:aa); phenotype 3:1.
When it triggers
Question asks for one ratio while presenting cross details.
How to avoid
Always note dominance: phenotype merges Aa + AA; genotype keeps them separate.
Lesson: Mendelian Disorders Pedigree
Category: Similar Terms
Both haemophilia and colour blindness are X-linked recessive with carrier-mother transmission, so their pedigree descriptions and statistics get swapped.
When it triggers
A question gives the pedigree of one disorder (e.g., 8% of males affected, 0.4% of females) and asks which disease it is, with haemophilia offered as a distractor to the correct answer, colour blindness, or vice versa.
How to avoid
Colour blindness occurs in about 8% of males and 0.4% of females due to defective red/green cone genes on the X chromosome; haemophilia is a distinct X-linked recessive clotting-protein disorder, famously traced through Queen Victoria's pedigree, with no incidence percentage given in the text.
Lesson: Mendelian Disorders Pedigree
Category: Similar Terms
Students confuse thalassemia's quantitative globin-synthesis defect with sickle-cell anaemia's qualitative structural defect, or mix up which is X-linked vs autosomal.
When it triggers
A question asks which disorder involves 'too little normal globin produced' vs 'an incorrectly functioning globin protein' and swaps thalassemia and sickle-cell anaemia, or claims either is sex-linked.
How to avoid
Thalassemia is an autosome-linked recessive disease that is a quantitative problem — too few globin molecules synthesised (alpha chain via HBA1/HBA2 on chromosome 16, beta chain via HBB on chromosome 11); sickle-cell anaemia is also autosome-linked recessive but is a qualitative problem — an incorrectly functioning (sickle-shaped) globin from a Glu-to-Val substitution at the sixth position of the beta chain.
Lesson: Natural Selection Drift
Category: Similar Terms
Allopatric: geographic isolation. Sympatric: same area, no physical barrier (e.g. polyploidy in plants, host-shift).
When it triggers
Question gives speciation scenario and asks which type.
How to avoid
If geographic barrier mentioned → allopatric. If population overlaps → sympatric.
Lesson: Sex Determination Linkage
Category: Similar Terms
X-linked recessive (haemophilia, colour-blindness): affects males predominantly; carrier mother → 50% sons affected; affected father → all daughters carriers but not affected.
When it triggers
Pedigree question; carrier vs affected.
How to avoid
Sex chromosomes: XX vs XY. Recessive on X needs both copies (XaXa) in female, only one (XaY) in male.
Lesson: DNA Replication
Root cause: concept gap
Correction
ALL DNA pol synthesises 5'→3'. Lagging strand uses Okazaki fragments to APPEAR to extend toward fork while each fragment grows 5'→3'.
Lesson: Genetic Code
Root cause: term confusion
Correction
The genetic code is degenerate because some amino acids are coded by more than one codon; it is unambiguous because each codon is read in mRNA in a contiguous fashion specifying only one amino acid, with no punctuations between codons.
Wrong option pattern
labels the code as 'ambiguous' or claims one codon can specify multiple amino acids
Lesson: Genetic Code
Root cause: rushed under time pressure
Correction
Only insertion or deletion of one or two bases (not a multiple of three) shifts the reading frame from that point onward; insertion or deletion of three bases or multiples of three only adds or removes whole codons, leaving the downstream reading frame unaltered.
Wrong option pattern
marks a 3-base or 6-base insertion/deletion as causing a frameshift
Lesson: Genetic Material DNA Packaging
Root cause: term confusion
Correction
Griffith (1928) demonstrated a 'transforming principle' without identifying it biochemically; Avery-MacLeod-McCarty (1933-44) showed DNA alone causes transformation biochemically; Hershey and Chase (1952) gave the unequivocal proof using radiolabeled bacteriophages.
Wrong option pattern
selects Griffith or Avery-MacLeod-McCarty as the 'unequivocal proof' source instead of Hershey-Chase
Lesson: Genetic Material DNA Packaging
Root cause: concept gap
Correction
DNA is chemically less reactive and structurally more stable than RNA because RNA's 2'-OH group is reactive and RNA is also catalytic; the presence of thymine instead of uracil confers additional stability to DNA, making DNA the preferred molecule for storage of genetic information.
Wrong option pattern
claims RNA is more stable than DNA or that thymine is less stabilising than uracil
Lesson: Hardy Weinberg Principle
Root cause: formula misuse
Correction
Genotype frequencies: p² (AA) + 2pq (Aa) + q² (aa) = 1. Allele frequencies: p + q = 1. Don't drop 2pq.
Lesson: Mendelian Disorders Pedigree
Root cause: concept gap
Correction
Mendelian disorders (e.g. haemophilia, cystic fibrosis, sickle-cell anaemia, colour blindness, phenylketonuria, thalassemia) are caused by alteration/mutation in a single gene and are traced by pedigree analysis, whereas chromosomal disorders are caused by absence, excess or abnormal arrangement of whole chromosomes — this lesson covers only the Mendelian category.
Wrong option pattern
lists Down's syndrome or Turner's syndrome as an example of a Mendelian disorder
Lesson: Mendelian Disorders Pedigree
Root cause: concept gap
Correction
The mother is not herself colour blind (or haemophilic) because the gene is recessive and its effect is suppressed by her matching dominant normal gene on the other X chromosome; she can still transmit the trait to sons with 50 per cent probability.
Wrong option pattern
claims a heterozygous carrier mother shows partial or mild symptoms of the disorder
Lesson: Mutations Genetic Disorders
Root cause: concept gap
Correction
Frameshift = ANY indel NOT divisible by 3 (since codons are triplets). Indels of 3, 6, 9... preserve reading frame.
Lesson: Transcription Translation
Root cause: term confusion
Correction
Start codon: AUG (Met / fMet). Stop codons: UAA (ochre), UAG (amber), UGA (opal/umber).
Formulas in this unit
Lesson: Hardy Weinberg Principle
Hardy-Weinberg equation
In an idealised population (no mutation, drift, selection, gene flow, random mating), allele and genotype frequencies remain constant.
| Symbol | Quantity | SI Unit |
|---|---|---|
| p | freq of dominant allele A | - |
| q | freq of recessive allele a | - |
Valid when
- Idealised population
- All five conditions met
- Diploid, autosomal, biallelic locus
Lesson: Linkage Recombination Mapping
Recombination frequency (genetic mapping)
Proportion of recombinant offspring measures genetic distance between linked loci. Capped at 50% (independent assortment).
| Symbol | Quantity | SI Unit |
|---|---|---|
| RF | recombination frequency | % |
Valid when
- Linked loci on same chromosome
Lesson: Mendel Inheritance
Mendel's monohybrid ratio
F2 ratio in monohybrid cross — products of independent assortment of two alleles per locus.
| Symbol | Quantity | SI Unit |
|---|---|---|
| ratio | F2 progeny ratio | - |
Valid when
- Single gene with complete dominance
- Pure-bred parents
Lesson: Mendel Inheritance
Mendel's dihybrid ratio
F2 ratio in dihybrid cross with two independently-segregating loci, complete dominance, no linkage.
| Symbol | Quantity | SI Unit |
|---|---|---|
| ratio | F2 phenotype ratio | - |
Valid when
- Two unlinked loci
- Complete dominance
NEET question patterns in this unit
Unit-wide
Mendel, inheritance patterns, linkage, sex determination, mutations, DNA, evolution
Common distractors
similar term confusion
Biology relies on precise terminology; close terms tempt selection.
Questions about this unit
- What does Genetics and Evolution cover for NEET Biology?
- 18 lessons: DNA Replication, DNA RNA Structure, Evidences Evolution, Gene Regulation Lac Operon, Genetic Code, Genetic Material DNA Packaging, Hardy Weinberg Principle, Hominid Evolution, Human Genome Project, Incomplete Dominance Codominance, Linkage Recombination Mapping, Mendel Inheritance, Mendelian Disorders Pedigree, Mutations Genetic Disorders, Natural Selection Drift, Origin Life Panspermia, Sex Determination Linkage and Transcription Translation.
- How often has Genetics and Evolution come up in NEET past papers?
- Our set of verified past papers has 82 questions from this unit, from NEET 2020, 2021, 2022, 2023, 2024, 2025 and 2026. Each is answered against the official NTA key.
- Is the Genetics and Evolution material free?
- Yes. All 18 lessons and 144 practice questions are free, with no login needed.