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・ X-ray source
・ X-Ray Specs
・ X-Ray Specs (comic strip)
・ X-Ray Specs (novelty)
・ X-Ray Spectrometry (journal)
・ X-ray spectroscopy
・ X-Ray Spex
・ X-ray standing waves
・ X-ray star
・ X-ray telescope
・ X-ray transform
・ X-ray transient
・ X-ray tube
・ X-ray vision
・ X-Ray Vision (album)
X-linked dominant inheritance
・ X-linked endothelial corneal dystrophy
・ X-linked hypertrichosis
・ X-linked hypophosphatemia
・ X-linked ichthyosis
・ X-linked intellectual disability
・ X-linked lymphoproliferative disease
・ X-linked myotubular myopathy
・ X-linked recessive chondrodysplasia punctata
・ X-linked recessive hypoparathyroidism
・ X-linked recessive inheritance
・ X-linked reticulate pigmentary disorder
・ X-linked severe combined immunodeficiency
・ X-linked spinal muscular atrophy type 2
・ X-Lite


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X-linked dominant inheritance : ウィキペディア英語版
X-linked dominant inheritance

X-linked dominant inheritance, sometimes referred to as X-linked dominance, is a mode of genetic inheritance by which a dominant gene is carried on the X chromosome. As an inheritance pattern, it is less common than the X-linked recessive type. In medicine, X-linked dominant inheritance indicates that a gene responsible for a genetic disorder is located on the X chromosome, and only one copy of the allele is sufficient to cause the disorder when inherited from a parent who has the disorder.
X-linked dominant traits do not necessarily affect males more than females (unlike X-linked recessive traits). The exact pattern of inheritance varies, depending on whether the father or the mother has the trait of interest. All daughters of an affected father will also be affected but none of his sons will be affected (unless the mother is also affected). In addition, the mother of an affected son is also affected (but not necessarily the other way round).
Some scholars have suggested discontinuing the terms dominant and recessive when referring to X-linked inheritance due to the multiple mechanisms that can result in the expression of X-linked traits in females, which include cell autonomous expression, skewed X-inactivation, clonal expansion, and somatic mosaicism.
==Genetics==
As the X chromosome is one of the sex chromosomes (the other being the Y chromosome), X-linked
inheritance is determined by the sex of the parent carrying a specific gene and can often seem complex. This is due to the fact that, typically, females have two copies of the X-chromosome, while males have only one copy. The difference between dominant and recessive inheritance patterns also plays a role in determining the chances of a child inheriting an X-linked disorder from their parentage.
Males can only get an X chromosome from their mother whilst females get an X chromosome from both parents. As a result, females tend to show higher prevalence of X-linked dominant disorders because they have more of a chance to inherit a faulty X chromosome.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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