Genetics Symbols Table

Standard Notation for Alleles, Pedigrees, and Chromosomes.

Aa

Alleles & Genotypes

T
Alleles

Dominant Allele

An allele that expresses its trait even when only one copy is present.

ExampleTall Plants (T)
t
Alleles

Recessive Allele

An allele that is expressed only when two copies are present (homozygous).

ExampleDwarf Plants (t)
TT
Genotypes

Homozygous Dominant

Genotype with two identical dominant alleles.

ExampleTT (Tall)
tt
Genotypes

Homozygous Recessive

Genotype with two identical recessive alleles.

Examplett (Dwarf)
Tt
Genotypes

Heterozygous

Genotype with two different alleles (one dominant, one recessive).

ExampleTt (Tall)
F1

Generations & Pedigree

P
Generations

Parental Generation

The initial generation in a genetic cross.

ExampleParents
F1
Generations

First Filial Generation

The first generation of offspring from the P generation.

ExampleChildren
F2
Generations

Second Filial Generation

The offspring produced by interbreeding the F1 generation.

ExampleGrandchildren
Pedigree

Male (Pedigree)

Square symbol represents a male family member.

ExampleFather
Pedigree

Female (Pedigree)

Circle symbol represents a female family member.

ExampleMother
XY

Chromosomes & DNA

XX
Chromosomes

Female Chromosomes

Sex chromosome pair responsible for female biological sex in humans.

ExampleFemale
XY
Chromosomes

Male Chromosomes

Sex chromosome pair responsible for male biological sex in humans.

ExampleMale
XᶜXᶜ
X-Linked

Affected Female

Note for X-linked recessive traits (like Colorblindness).

ExampleColorblind Female
XᶜY
X-Linked

Affected Male

Male with X-linked recessive trait (Hemizygous).

ExampleColorblind Male
A-T
DNA Bases

Adenine-Thymine

Complementary base pair in DNA double helix.

ExampleDNA Structure
G-C
DNA Bases

Guanine-Cytosine

Complementary base pair in DNA and RNA.

ExampleStronger Bond (3 H-bonds)
U
DNA Bases

Uracil

Nitrogenous base found only in RNA (Replaces Thymine).

ExampleRNA

Reading the Language of Life

Genetics relies on specific symbols to map the flow of traits from parents to offspring. Understanding these abbreviations is key to solving problems in inheritance and heredity.

The Punnett Square Grid

Visualizing a Hybrid Cross (Tt x Tt)

A classic Mendelian cross between two Tall Hybrid plants. This predicts the probability of offspring genotypes.

  • 25% Homozygous Dominant (TT)
  • 50% Heterozygous (Tt)
  • 25% Homozygous Recessive (tt)
T (Dad)
t (Dad)
T (Mom)
TT
Tt
t (Mom)
Tt
tt

Pedigree Chart Legend

Male(UNAFFECTED)
Female(UNAFFECTED)
Male(AFFECTED)
Female(AFFECTED)

Frequently Asked Questions

What is the difference between Heterozygous and Homozygous?

Homozygous means having two identical alleles (e.g., TT or tt). Heterozygous means having two different alleles (e.g., Tt), where the dominant allele typically masks the recessive one.

How are males and females represented in a pedigree chart?

In pedigree charts, a Square (□) represents a Male, and a Circle (○) represents a Female. A shaded shape usually indicates an individual affected by the trait being tracked.

What does "F1 Generation" stand for?

F1 stands for "First Filial" generation. It refers to the first set of offspring produced by the parental (P) generation cross.

Why are dominant alleles written in capital letters?

Capital letters (e.g., T) are used by convention to show that the allele is Dominant and will express its trait over a recessive allele (lowercase, e.g., t).

What is a "Carrier"?

A Carrier is a heterozygous individual (e.g., XᶜX) who carries a recessive allele for a genetic disorder but does not show symptoms. They can pass the allele to their offspring.

What do the letters A, T, G, and C stand for?

They represent the four nitrogenous bases of DNA: Adenine (A), Thymine (T), Guanine (G), and Cytosine (C). A always pairs with T, and G always pairs with C.

How is X-linked inheritance noticed?

X-linked recessive traits (like colorblindness) are more common in Males (XY) because they only have one X chromosome. If that single X has the recessive gene, they express the trait.

What is a Genotype vs Phenotype?

Genotype is the genetic makeup (e.g., Tt). Phenotype is the physical appearance resulting from that genotype (e.g., Tall Plant).

What does "n" and "2n" mean?

n represents a Haploid cell (one set of chromosomes, e.g., gametes). 2n represents a Diploid cell (two sets of chromosomes, e.g., body cells).

Does "Dominant" mean "Most Common"?

No. Dominant only means the allele masks the recessive one. It does not necessarily mean the trait is more common in a population (e.g., Huntingtons disease is dominant but rare).