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  2. X-inactivation - Wikipedia

    en.wikipedia.org/wiki/X-inactivation

    Theoretically, X-inactivation should eliminate the differences in gene dosage between affected individuals and individuals with a typical chromosome complement. In affected individuals, however, X-inactivation is incomplete and the dosage of these non-silenced genes will differ as they escape X-inactivation, similar to an autosomal aneuploidy.

  3. Barr body - Wikipedia

    en.wikipedia.org/wiki/Barr_body

    Barr bodies can be seen in neutrophils at the rim of the nucleus. In humans with more than one X chromosome, the number of Barr bodies visible at interphase is always one fewer than the total number of X chromosomes. For example, people with Klinefelter syndrome (47, XXY) have a single Barr body, and people with a 47, XXX karyotype have two ...

  4. X-chromosome reactivation - Wikipedia

    en.wikipedia.org/wiki/X-chromosome_reactivation

    X chromosome reactivation (XCR) is the process by which the inactive X chromosome (the Xi) is re-activated in the cells of eutherian female mammals. Therian female mammalian cells have two X chromosomes, while males have only one, requiring X-chromosome inactivation (XCI) for sex-chromosome dosage compensation .

  5. Sex-chromosome dosage compensation - Wikipedia

    en.wikipedia.org/wiki/Sex-chromosome_dosage...

    Not all random X-inactivation is entirely random. Some alleles, generally mutations in the X-inactivation center on the X-chromosome have been demonstrated to confer a bias towards inactivation for the chromosome on which they sit. [1] Truly random X-inactivation may also appear to be non-random if one X-chromosome carries a deleterious mutation.

  6. Skewed X-inactivation - Wikipedia

    en.wikipedia.org/wiki/Skewed_X-inactivation

    Skewed X-inactivation has medical significance due to its impacts on X-linked diseases. X-chromosome skewing has an ability to amplify diseases on the X chromosome. In wildtype women, recessive diseases on the X chromosome are often unexpressed due to the roughly even inactivation process, which prevents mutated alleles from becoming heavily ...

  7. Hypohidrotic ectodermal dysplasia - Wikipedia

    en.wikipedia.org/wiki/Hypohidrotic_ectodermal...

    In X-linked recessive inheritance, a female with one altered copy of the gene in each cell is called a carrier. Since females operate on only one of their two X chromosomes (X inactivation) a female carrier may or may not manifest symptoms of the disease. If a female carrier is operating on her normal X she will not show symptoms.

  8. X chromosome - Wikipedia

    en.wikipedia.org/wiki/X_chromosome

    This phenomenon is called X-inactivation or Lyonization, and creates a Barr body. If X-inactivation in the somatic cell meant a complete de-functionalizing of one of the X-chromosomes, it would ensure that females, like males, had only one functional copy of the X chromosome in each somatic cell. This was previously assumed to be the case.

  9. Karyotype - Wikipedia

    en.wikipedia.org/wiki/Karyotype

    X-inactivation. The inactivation of one X chromosome takes place during the early development of mammals (see Barr body and dosage compensation). In placental mammals, the inactivation is random as between the two Xs; thus the mammalian female is a mosaic in respect of her X chromosomes. In marsupials it