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  2. Mendelian inheritance - Wikipedia

    en.wikipedia.org/wiki/Mendelian_inheritance

    In a dominant-recessive inheritance, an average of 25% are homozygous with the dominant trait, 50% are heterozygous showing the dominant trait in the phenotype (genetic carriers), 25% are homozygous with the recessive trait and therefore express the recessive trait in the phenotype. The genotypic ratio is 1: 2 : 1, and the phenotypic ratio is 3: 1.

  3. Mendelian traits in humans - Wikipedia

    en.wikipedia.org/wiki/Mendelian_traits_in_humans

    Mendelian traits in humans. A 50/50 chance of inheritance. Sickle-cell disease is inherited in the autosomal recessive pattern. When both parents have sickle-cell trait (carrier), a child has a 25% chance of sickle-cell disease (red icon), 25% do not carry any sickle-cell alleles (blue icon), and 50% have the heterozygous (carrier) condition. [1]

  4. Human genetics - Wikipedia

    en.wikipedia.org/wiki/Human_genetics

    Human genetics. Human genetics is the study of inheritance as it occurs in human beings. Human genetics encompasses a variety of overlapping fields including: classical genetics, cytogenetics, molecular genetics, biochemical genetics, genomics, population genetics, developmental genetics, clinical genetics, and genetic counseling.

  5. Dominance (genetics) - Wikipedia

    en.wikipedia.org/wiki/Dominance_(genetics)

    In genetics, dominance is the phenomenon of one variant (allele) of a gene on a chromosome masking or overriding the effect of a different variant of the same gene on the other copy of the chromosome. [1][2] The first variant is termed dominant and the second is called recessive. This state of having two different variants of the same gene on ...

  6. Punnett square - Wikipedia

    en.wikipedia.org/wiki/Punnett_square

    The Punnett square is a square diagram that is used to predict the genotypes of a particular cross or breeding experiment. It is named after Reginald C. Punnett, who devised the approach in 1905. [3][4][5][6][7][8] The diagram is used by biologists to determine the probability of an offspring having a particular genotype.

  7. Genotype - Wikipedia

    en.wikipedia.org/wiki/Genotype

    Category. v. t. e. The genotype of an organism is its complete set of genetic material. [1] Genotype can also be used to refer to the alleles or variants an individual carries in a particular gene or genetic location. [2] The number of alleles an individual can have in a specific gene depends on the number of copies of each chromosome found in ...

  8. Introduction to genetics - Wikipedia

    en.wikipedia.org/wiki/Introduction_to_genetics

    For example, rice can be given genes from a maize and a soil bacteria so the rice produces beta-carotene, which the body converts to vitamin A. [19] This can help children with Vitamin A deficiency. Another gene being put into some crops comes from the bacterium Bacillus thuringiensis; the gene makes a protein that is an insecticide.

  9. Simple Mendelian genetics in humans - Wikipedia

    en.wikipedia.org/wiki/Simple_Mendelian_genetics...

    OMIM (Online Mendelian Inheritance in Man) [3] is a comprehensive database of human genotype–phenotype links. Many visible human traits that exhibit high heritability were included in the older McKusick's Mendelian Inheritance in Man. Before the discovery of genotyping, they were used as genetic markers in medicolegal practice, including in ...