| Term | Definition | NEET Context |
|---|---|---|
| Allele | Alternative forms of a gene at the same chromosomal locus | "Mendel's factors" — each gene has 2 alleles per individual |
| Dominant allele | Allele that is expressed in both homozygous and heterozygous conditions | Represented by uppercase letter (T, R, A) |
| Recessive allele | Allele expressed only in homozygous condition; masked by dominant allele | Represented by lowercase letter (t, r, a) |
| Homozygous | Both alleles at a locus are identical (TT or tt) | Also called "pure-breeding" or "true-breeding" |
| Heterozygous | Two different alleles at a locus (Tt) | Also called "hybrid" or "carrier" |
| Phenotype | Observable physical expression of a trait | Depends on genotype + environment |
| Genotype | Genetic constitution — which alleles are present | Not always visible; needs test cross or molecular analysis |
| Monohybrid cross | Cross involving one pair of contrasting traits | Produces 3:1 (F2) or 1:1 (test cross) ratios |
| Dihybrid cross | Cross involving two pairs of contrasting traits | Produces 9:3:3:1 (F2) or 1:1:1:1 (test cross) |
| Test cross | Crossing unknown dominant phenotype with homozygous recessive to determine genotype | 1:1 → heterozygous; all dominant → homozygous dominant |
| Back cross | F1 offspring crossed with a parent; includes test cross | Broader term; test cross is a specific back cross |
| F1 generation | First filial generation — offspring of P (parental) cross | All Tt in Mendel's monohybrid crosses |
| F2 generation | Second filial generation — offspring of F1 × F1 cross | Shows classical Mendelian ratios |
| Incomplete dominance | Heterozygote shows intermediate/blended phenotype | Pink snapdragons (Rr); F2 = 1:2:1 |
| Co-dominance | Both alleles fully expressed simultaneously in heterozygote | Blood group AB ( ) |
| Multiple alleles | More than 2 alleles for one gene existing in a population | ABO: , , i (3 alleles in population) |
| Pleiotropy | One gene affecting multiple unrelated traits | HbS allele → sickle cell anemia affecting multiple systems |
| Polygenic inheritance | Multiple genes with additive effects controlling one trait | Skin colour, height — continuous variation |
| Linkage | Genes on same chromosome tend to be inherited together | Exception to Law of Independent Assortment |
| Recombination | New allele combinations created by crossing over during meiosis I | Produces recombinant offspring in test crosses |
| Epistasis | One gene masks or modifies expression of another gene | Produces modified dihybrid ratios (9:7, 12:3:1, etc.) |
| Centimorgan (cM) | Unit of genetic distance = 1% recombination frequency | 1 cM = 1 map unit; named after T.H. Morgan |
| Geitonogamy | Pollination between different flowers on the same plant | Genetically equivalent to self-pollination in homozygous plants |
| Emasculation | Removal of stamens to prevent self-pollination | Mendel's technique for controlled cross-pollination |
| Chiasma | X-shaped structure where crossing over occurs between non-sister chromatids | Forms during pachytene of Prophase I; plural = chiasmata |
Part of GEN-01 — Mendelian Genetics & Inheritance Patterns
Glossary — Key Terms with NEET Definitions
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