Each gene occupies a specific position on the type of chromosome where it is located. This position is called the locus of the gene.
Alleles can be dominant or recessive, with only one copy needed to express the trait.
The alleles are alternative forms of genes that code for different versions of the same protein or trait.
Dominant alleles mask the expression of recessive alleles.
New alleles are formed from other alleles by gene mutation.
The genome is the whole of the genetic information of an organism.
In humans the genome consists of the 46 molecules that form the chromosomes in the nucleus plus the DNA molecule in the mitochondrion.
The genome of prokaryotes is much smaller and consists of the DNA in the circular chromosome, plus any plasmids that are present.
A gene is a sequence of bases on a DNA molecule that codes for a protein.
Genotype is the genetic constitution of an individual (i.e. all the alleles that an individual has).
Phenotype is the set of observable characteristics of an individual, resulting from the interaction of its genotype with the environment.
Diploid is a term that refers to the presence of two complete sets of chromosomes in an organism's cells, with each parent contributing a chromosome to each pair.
A karyotype is an individual's complete set of chromosomes.
An autosome is one of the numbered chromosomes, as opposed to the sex chromosomes.
Humans have 22 pairs of autosomes and one pair of sex chromosomes (XX or XY).
Homozygous - the presence of two identical alleles at a particular gene locus.
Heterozygous - having inherited different versions (alleles) of a genomic marker from each biological parent.
The characteristic of a dominant allele is present even if only one allele is present.
The characteristic of a recessive allele is present only if both alleles are present.
Mendelian inheritance refers to an inheritance pattern that follows the laws of segregation and independent assortment in which a gene inherited from either parent segregates into gametes at an equal frequency.
Incomplete dominance is a condition in which a dominant allele does not completely mask the effects of a recessive allele.
In an X-linked disease the defective gene is present on the X chromosome and therefore, males are more likely to inherit the defective gene.
Codominant inheritance occurs when two alleles contribute equally to the expression of a particular trait.