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  2. Allele - Wikipedia

    en.wikipedia.org/wiki/Allele

    Allele. An allele[1], or allelomorph, is a variant of the sequence of nucleotides at a particular location, or locus, on a DNA molecule. [2] Alleles can differ at a single position through single nucleotide polymorphisms (SNP), [3] but they can also have insertions and deletions of up to several thousand base pairs. [4]

  3. Phenotypic trait - Wikipedia

    en.wikipedia.org/wiki/Phenotypic_trait

    Thus you can tell that each allele is present in the heterozygote. [9] Codominance refers to the allelic relationship that occurs when two alleles are both expressed in the heterozygote, and both phenotypes are seen simultaneously. [10] Multiple alleles refers to the situation when there are more than 2 common alleles of a particular gene.

  4. Ploidy - Wikipedia

    en.wikipedia.org/wiki/Ploidy

    If a haploid set consists of two sets, it must be of a tetraploid (four sets) species. [1] Ploidy (/ ˈplɔɪdi /) is the number of complete sets of chromosomes in a cell, and hence the number of possible alleles for autosomal and pseudoautosomal genes. Here sets of chromosomes refers to the number of maternal and paternal chromosome copies ...

  5. Non-Mendelian inheritance - Wikipedia

    en.wikipedia.org/wiki/Non-Mendelian_inheritance

    In Mendelian inheritance, genes have only two alleles, such as a and A. Mendel consciously chose pairs of genetic traits, represented by two alleles for his inheritance experiments. In nature, such genes often exist in several different forms and are therefore said to have multiple alleles. An individual usually has only two copies of each gene ...

  6. Locus (genetics) - Wikipedia

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

    Locus (genetics) In genetics, a locus (pl.: loci) is a specific, fixed position on a chromosome where a particular gene or genetic marker is located. [1] Each chromosome carries many genes, with each gene occupying a different position or locus; in humans, the total number of protein-coding genes in a complete haploid set of 23 chromosomes is ...

  7. Haplotype - Wikipedia

    en.wikipedia.org/wiki/Haplotype

    A haplotype (haploid genotype) is a group of alleles in an organism that are inherited together from a single parent. [1][2] Many organisms contain genetic material (DNA) which is inherited from two parents. Normally these organisms have their DNA organized in two sets of pairwise similar chromosomes. The offspring gets one chromosome in each ...

  8. Quantitative genetics - Wikipedia

    en.wikipedia.org/wiki/Quantitative_genetics

    The progeny line with both the "more" and the "less" alleles present in equal frequency (k = 4) had a mean below the overall average (see next paragraph), and had the lowest level of homozygosity. These results reveal the fact that the alleles most prevalent in the "gene-pool" (also called the "germplasm") determine performance, not the level ...

  9. Allele frequency - Wikipedia

    en.wikipedia.org/wiki/Allele_frequency

    Allele frequency. Allele frequency, or gene frequency, is the relative frequency of an allele (variant of a gene) at a particular locus in a population, expressed as a fraction or percentage. [1] Specifically, it is the fraction of all chromosomes in the population that carry that allele over the total population or sample size.