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Extranuclear inheritance (also known as cytoplasmic inheritance) is a form of non-Mendelian inheritance also first discovered by Carl Correns in 1908. [9] While working with Mirabilis jalapa, Correns observed that leaf colour was dependent only on the genotype of the maternal parent.
Uniparental inheritance is a non-Mendelian form of inheritance that consists of the transmission of genotypes from one parental type to all progeny. That is, all the genes in offspring will originate from only the mother or only the father.
Lethal alleles may specifically refer to embryonically lethal alleles, in which the fetus will never survive to term. Such alleles are a cause of non-Mendelian patterns of inheritance, such as the observation of traits in a 2:1 ratio.
In genetics, paternal mtDNA transmission and paternal mtDNA inheritance refer to the incidence of mitochondrial DNA (mtDNA) being passed from a father to his offspring. . Paternal mtDNA inheritance is observed in a small proportion of species; in general, mtDNA is passed unchanged from a mother to her offspring, [1] making it an example of non-Mendelian inh
A polygene is a member of a group of non-epistatic genes that interact additively to influence a phenotypic trait, thus contributing to multiple-gene inheritance (polygenic inheritance, multigenic inheritance, quantitative inheritance [1]), a type of non-Mendelian inheritance, as opposed to single-gene inheritance, which is the core notion of Mendelian inheritance.
Biparental inheritance is a type of biological inheritance where the progeny inherits a maternal and a paternal allele for one gene. It is one of the criteria for Mendelian inheritance . Sexual reproduction , where offspring result from the fusion of gametes from two parents, is the most common form of biparental inheritance.
[7] [8] In 2014, there were about 150 imprinted genes known in mice and about half that in humans. [9] As of 2019, 260 imprinted genes have been reported in mice and 228 in humans. [10] Genomic imprinting is an inheritance process independent of the classical Mendelian inheritance. [11]
Chromosomal inheritance follows normal Mendelian laws, despite the fact that the phenotype of the disease may be masked. Because of the complex ways in which mitochondrial and nuclear DNA "communicate" and interact, even seemingly simple inheritance is hard to diagnose.