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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. Human evolutionary genetics - Wikipedia

    en.wikipedia.org/wiki/Human_evolutionary_genetics

    The human genome has been sequenced, as well as the chimpanzee genome. Humans have 23 pairs of chromosomes, while chimpanzees, gorillas and orangutans have 24. Human chromosome 2 is a fusion of two chromosomes 2a and 2b that remained separate in the other primates. [9]

  6. Karyotype - Wikipedia

    en.wikipedia.org/wiki/Karyotype

    Differences in basic number of chromosomes. These differences could have resulted from successive unequal translocations which removed all the essential genetic material from a chromosome, permitting its loss without penalty to the organism (the dislocation hypothesis) or through fusion. Humans have one pair fewer chromosomes than the great apes.

  7. Genotype - Wikipedia

    en.wikipedia.org/wiki/Genotype

    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 chromosomes are present, meaning each individual has two alleles for any given gene.

  8. Patau syndrome - Wikipedia

    en.wikipedia.org/wiki/Patau_syndrome

    This can occur either because each cell contains a full extra copy of chromosome 13 (a disorder known as trisomy 13 or trisomy D or T13 [1]), or because each cell contains an extra partial copy of the chromosome, or because there are two different lines of cells—one healthy with the correct number of chromosomes 13 and one that contains an ...

  9. List of organisms by chromosome count - Wikipedia

    en.wikipedia.org/wiki/List_of_organisms_by...

    The list of organisms by chromosome count describes ploidy or numbers of chromosomes in the cells of various plants, animals, protists, and other living organisms. This number, along with the visual appearance of the chromosome, is known as the karyotype, [1] [2] [3] and can be found by looking at the chromosomes through a microscope.