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  2. Zygosity - Wikipedia

    en.wikipedia.org/wiki/Zygosity

    An individual that is homozygous-recessive for a particular trait carries two copies of the allele that codes for the recessive trait. This allele, often called the "recessive allele", is usually represented by the lowercase form of the letter used for the corresponding dominant trait (such as, with reference to the example above, "p" for the ...

  3. Test cross - Wikipedia

    en.wikipedia.org/wiki/Test_cross

    Since the homozygous recessive individual can only pass on recessive alleles, the allele the individual in question passes on determines the phenotype of the offspring. [3] Thus, this test yields 2 possible situations: If any of the offspring produced express the recessive trait, the individual in question is heterozygous for the dominant ...

  4. Monohybrid cross - Wikipedia

    en.wikipedia.org/wiki/Monohybrid_cross

    Figure 1: Inheritance pattern of dominant (red) and recessive (white) phenotypes when each parent (1) is homozygous for either the dominant or recessive trait. All members of the F 1 generation are heterozygous and share the same dominant phenotype (2), while the F 2 generation exhibits a 6:2 ratio of dominant to recessive phenotypes (3).

  5. Genotype - Wikipedia

    en.wikipedia.org/wiki/Genotype

    Finally, the offspring could inherit a recessive allele from each parent, making them homozygous with a genotype of bb. Plants with the BB and Bb genotypes will look the same, since the B allele is dominant. The plant with the bb genotype will have the recessive trait.

  6. Punnett square - Wikipedia

    en.wikipedia.org/wiki/Punnett_square

    The phenotype of a homozygous dominant pair is 'A', or dominant, while the opposite is true for homozygous recessive. Heterozygous pairs always have a dominant phenotype. [11] To a lesser degree, hemizygosity [12] and nullizygosity [13] can also be seen in gene pairs.

  7. Obligate carrier - Wikipedia

    en.wikipedia.org/wiki/Obligate_carrier

    In X-linked recessive disorders, only females can be the carriers of the recessive mutation, making them obligate carriers of this type of disease. Females acquire one X-chromosome from their father and one from their mother, and this means they can either be heterozygous for the mutated allele or homozygous. If heterozygous, she is a carrier ...

  8. ABCC11 - Wikipedia

    en.wikipedia.org/wiki/ABCC11

    The homozygous recessive AA genotype produces the dry ear wax phenotype (dry and flaky) and mildly odored sweat. [ 9 ] The alleles containing a guanine produce a protein that is glycosylated but alleles containing an adenine are not glycosylated.

  9. Three-point cross - Wikipedia

    en.wikipedia.org/wiki/Three-point_cross

    An individual heterozygous for three mutations is crossed with a homozygous recessive individual, and the phenotypes of the progeny are scored. The two most common phenotypes that result are the parental gametes; the two least common phenotypes that result come from a double crossover in gamete formation. By comparing the parental and double ...