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  2. Allele - Wikipedia

    en.wikipedia.org/wiki/Allele

    A null allele is a gene variant that lacks the gene's normal function because it either is not expressed, or the expressed protein is inactive. For example, at the gene locus for the ABO blood type carbohydrate antigens in humans, [13] classical genetics recognizes three alleles, I A, I B, and i, which determine compatibility of blood transfusions.

  3. Locus (genetics) - Wikipedia

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

    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 estimated at 19,000–20,000. [2] Genes may possess multiple variants known as alleles, and an allele may also be said to reside at a particular locus.

  4. Introduction to genetics - Wikipedia

    en.wikipedia.org/wiki/Introduction_to_genetics

    As an example, one allele for the gene for hair color could instruct the body to produce much pigment, producing black hair, while a different allele of the same gene might give garbled instructions that fail to produce any pigment, giving white hair. Mutations are random changes in genes and can create new alleles. Mutations can also produce ...

  5. Genotype - Wikipedia

    en.wikipedia.org/wiki/Genotype

    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 that species, also referred to as ploidy. In diploid species like humans, two full sets of ...

  6. Genetic linkage - Wikipedia

    en.wikipedia.org/wiki/Genetic_linkage

    Genetic linkage is the tendency of DNA sequences that are close together on a chromosome to be inherited together during the meiosis phase of sexual reproduction.Two genetic markers that are physically near to each other are unlikely to be separated onto different chromatids during chromosomal crossover, and are therefore said to be more linked than markers that are far apart.

  7. Genomic imprinting - Wikipedia

    en.wikipedia.org/wiki/Genomic_imprinting

    Each autosomal gene is therefore represented by two copies, or alleles, with one copy inherited from each parent at fertilization. The expressed allele is dependent upon its parental origin. For example, the gene encoding insulin-like growth factor 2 (IGF2/Igf2) is only expressed from the allele inherited from the male. Although imprinting ...

  8. Gene - Wikipedia

    en.wikipedia.org/wiki/Gene

    A gene can acquire mutations in its sequence, leading to different variants, known as alleles, in the population. These alleles encode slightly different versions of a gene, which may cause different phenotypical traits. [4] Genes evolve due to natural selection or survival of the fittest and genetic drift of the alleles.

  9. Gene nomenclature - Wikipedia

    en.wikipedia.org/wiki/Gene_nomenclature

    Gene nomenclature is the scientific naming of genes, ... Rules for Nomenclature of Genes, Genetic Markers, Alleles, and Mutations in Mouse and Rat: