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  2. X-inactivation - Wikipedia

    en.wikipedia.org/wiki/X-inactivation

    The result is that the choice of inactivated X chromosome in all the cells of the organism is a random distribution, often with about half the cells having the paternal X chromosome inactivated and half with an inactivated maternal X chromosome; but commonly, X-inactivation is unevenly distributed across the cell lines within one organism ...

  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. 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.

  5. 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 .

  6. 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.

  7. Tsix - Wikipedia

    en.wikipedia.org/wiki/Tsix

    n/a Ensembl ENSG00000270641 n/a UniProt n a n/a RefSeq (mRNA) n/a n/a RefSeq (protein) n/a n/a Location (UCSC) Chr X: 73.79 – 73.83 Mb n/a PubMed search n/a Wikidata View/Edit Human Simplified flowchart of Tsix's role in Xist gene function Tsix is a non-coding RNA gene that is antisense to the Xist RNA. Tsix binds Xist during X chromosome inactivation. The name Tsix comes from the reverse of ...

  8. XIST - Wikipedia

    en.wikipedia.org/wiki/Xist

    Xist (X-inactive specific transcript) is a non-coding RNA transcribed from the X chromosome of the placental mammals that acts as a major effector of the X-inactivation process. [5] It is a component of the Xic – X-chromosome inactivation centre [6] – along with two other RNA genes (Jpx and Ftx) and two protein genes (Tsx and Cnbp2). [7]

  9. Skewed X-inactivation - Wikipedia

    en.wikipedia.org/wiki/Skewed_X-inactivation

    A 2013 study also found skewed X-inactivation to be a factor that predisposes individuals to esophageal carcinomas. [10] It has been postulated that skewed X-inactivation might lead to a decrease in the expression of X-linked tumor suppressor genes in an individual who also has a germline mutation in the expressed chromosome. This would cause ...