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  2. Chromosome 2 - Wikipedia

    en.wikipedia.org/wiki/Chromosome_2

    Chromosome 2 is one of the twenty-three pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 2 is the second-largest human chromosome, spanning more than 242 million base pairs [4] and representing almost eight percent of the total DNA in human cells. Chromosome 2 contains the HOXD homeobox gene cluster ...

  3. Human genome - Wikipedia

    en.wikipedia.org/wiki/Human_genome

    A major difference between the two genomes is human chromosome 2, which is equivalent to a fusion product of chimpanzee chromosomes 12 and 13. [110] (later renamed to chromosomes 2A and 2B, respectively).

  4. Chromosome 13 - Wikipedia

    en.wikipedia.org/wiki/Chromosome_13

    Trisomy 13 can also result from an extra copy of chromosome 13 in only some of the body's cells (mosaic trisomy 13). In a small percentage of cases, trisomy 13 is caused by a rearrangement of chromosomal material between chromosome 13 and another chromosome. As a result, a person has the two usual copies of chromosome 13, plus extra material ...

  5. Karyotype - Wikipedia

    en.wikipedia.org/wiki/Karyotype

    [33] [34] Thus, FN ≤ 2 × 2n, the difference depending on the number of chromosomes considered single-armed (acrocentric or telocentric) present. Humans have FN = 82, [35] due to the presence of five acrocentric chromosome pairs: 13, 14, 15, 21, and 22 (the human Y chromosome is also acrocentric).

  6. Chromosome - Wikipedia

    en.wikipedia.org/wiki/Chromosome

    This is an accepted version of this page This is the latest accepted revision, reviewed on 8 February 2025. DNA molecule containing genetic material of a cell This article is about the DNA molecule. For the genetic algorithm, see Chromosome (genetic algorithm). Chromosome (10 7 - 10 10 bp) DNA Gene (10 3 - 10 6 bp) Function A chromosome and its packaged long strand of DNA unraveled. The DNA's ...

  7. Zygosity - Wikipedia

    en.wikipedia.org/wiki/Zygosity

    A chromosome in a diploid organism is hemizygous when only one copy is present. [2] The cell or organism is called a hemizygote. Hemizygosity is also observed when one copy of a gene is deleted, or, in the heterogametic sex, when a gene is located on a sex chromosome.

  8. Secondary constriction - Wikipedia

    en.wikipedia.org/wiki/Secondary_constriction

    Secondary constrictions are the constricted or the narrow region found at any point of the chromosome other than that of centromere (primary constriction). The difference between the two constrictions can be noticed during anaphase, as chromosomes can only bend at the site of primary constriction. Secondary constrictions are useful in ...

  9. Robertsonian translocation - Wikipedia

    en.wikipedia.org/wiki/Robertsonian_translocation

    The most frequent forms of Robertsonian translocations are between chromosomes 13 and 14, 14 and 21, and 14 and 15. [2] A Robertsonian translocation results when the long arms of two acrocentric chromosomes fuse at the centromere and the two short arms are lost. If, for example, the long arms of chromosomes 13 and 14 fuse, no significant ...