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  2. 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 ...

  3. Punnett square - Wikipedia

    en.wikipedia.org/wiki/Punnett_square

    The Punnett square is a visual representation of Mendelian inheritance, a fundamental concept in genetics discovered by Gregor Mendel. [10] For multiple traits, using the "forked-line method" is typically much easier than the Punnett square. Phenotypes may be predicted with at least better-than-chance accuracy using a Punnett square, but the ...

  4. List of genetic codes - Wikipedia

    en.wikipedia.org/wiki/List_of_genetic_codes

    The trematode mitochondrial code. The Scenedesmus obliquus mitochondrial code. The Thraustochytrium mitochondrial code. The Pterobranchia mitochondrial code. The candidate division SR1 and gracilibacteria code. The Pachysolen tannophilus nuclear code. The karyorelict nuclear code. The Condylostoma nuclear code.

  5. 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]

  6. Sex linkage - Wikipedia

    en.wikipedia.org/wiki/Sex_linkage

    Sex linked describes the sex-specific reading patterns of inheritance and presentation when a gene mutation (allele) is present on a sex chromosome (allosome) rather than a non-sex chromosome (autosome). In humans, these are termed X-linked recessive, X-linked dominant and Y-linked. The inheritance and presentation of all three differ depending ...

  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

    Genetics is the study of genes and tries to explain what they are and how they work. Genes are how living organisms inherit features or traits from their ancestors; for example, children usually look like their parents because they have inherited their parents' genes. Genetics tries to identify which traits are inherited and to explain how ...

  9. Monohybrid cross - Wikipedia

    en.wikipedia.org/wiki/Monohybrid_cross

    Monohybrid cross. A monohybrid cross is a cross between two organisms with different variations at one genetic locus of interest. [1][2] The character (s) being studied in a monohybrid cross are governed by two or multiple variations for a single location of a gene. Then carry out such a cross, each parent is chosen to be homozygous or true ...