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Allele: one of a pair of alternative forms of a gene that occur at a given locus in a chromosome. Codominance: Co dominance is the equal and independent expression of the two alleles of a trait when they are present together in an individual. Coenzyme: Substance necessary for the activity of an enzyme. Dominance: A condition in which one member of an allele pair is manifested to the exclusion of the other. Duplicate genes: Two or more independent genes present on different chromosomes which determine the same or nearly same phenotype. Epistasis: It is the phenomenon of masking or suppressing the expression of a gene by another nonallelic gene Epistatic gene: The gene which suppresses the expression of a non allelic gene is known as Epistatic gene. F1: The first filial generation; the first generation of descent from a given matting. F2: The second filial generation produced by selfing F1 individuals. Gamete: A mature male or female reproductive cell ( sperm or egg) Gene: A hereditary determinant of a specific biological function; a unit of inheritance (DNA) located in a fixed position on a chromosome. Genotype: the genetic constitution of an organism. Heterozygote: An organism with unlike members of any given pair of alleles that consequently produces unlike gametes. Homozygote: An individual in which the two copies of a gene are the same allele. Hypostatic gene: The gene or locus which is suppressed by the presence of non allelic gene is termed as Hypostatic gene. Incomplete dominance: Expression of two alleles in a heterozygote that allows the heterozygote to be distinguished from either of its homozygous parents Intergenic gene interection: Interaction between the alleles of the two different genes. Complementary genes: Those non-allelic genes which independently show a similar effect but produce a new trait when present together in the dominant form. Intragenic gene interection: Interaction between the alleles of the same gene. Lethal genes: Those genes which kill the organisms when they are able to express their effect. Lethal mutation: A mutation that renders an organism or a cell possessing it inviable. Monohybrid Cross: A cross between parents differing in only one trait or in which only one trait is being considered. Multiple alleles: Occurrence of a gene in more than two alternate forms. Phenotype: The observable characteristics of an organism. Pleiotropy: Condition in which the single gene influences more than one trait. Recessive: A term applied to one member of an allelic pair lacking the ability to manifest itself when the other of the dominant member is present. Segregation: The separation of paternal and maternal chromosomes from each other at meiosis; the separation of alleles from each other in heterozygotes during meiosis. Sickle Cell Anaemia: An autosomal hereditary disorder in which the erythrocytes become sickleshaped under oxygen deficiency. Supplementary genes: A pair of nonallelic genes, one of which produces its effect independently when in dominant state, while the other is able to produce a new trait along with the dominant allele of the former. Suppressor Genes: A nonallelic gene which does not produce any phenotypic expression of its own but suppresses the expression of a non allelic gene.