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سيادة مشتركة - ترجمة إلى إنجليزي
سيادة مشتركة
condominium
سيادة مشتركة
condominium (N)
codominance
![A and B blood types]] in humans show co-dominance, but the O type is recessive to A and B.](https://commons.wikimedia.org/wiki/Special:FilePath/ABO system codominance.svg?width=200 "A and B blood types]] in humans show co-dominance, but the O type is recessive to A and B.")
![Co-dominance in a [[Camellia]] cultivar](https://commons.wikimedia.org/wiki/Special:FilePath/Co-dominance Rhododendron.jpg?width=200 "Co-dominance in a [[Camellia]] cultivar")
![This [[Punnett square]] illustrates incomplete dominance. In this example, the red petal trait associated with the R [[allele]] recombines with the white petal trait of the r allele. The plant incompletely expresses the dominant trait (R) causing plants with the Rr genotype to express flowers with less red pigment resulting in pink flowers. The colors are not blended together, the dominant trait is just expressed less strongly.](https://commons.wikimedia.org/wiki/Special:FilePath/Incomplete dominance.svg?width=200 "This [[Punnett square]] illustrates incomplete dominance. In this example, the red petal trait associated with the R [[allele]] recombines with the white petal trait of the r allele. The plant incompletely expresses the dominant trait (R) causing plants with the Rr genotype to express flowers with less red pigment resulting in pink flowers. The colors are not blended together, the dominant trait is just expressed less strongly.")
 (14582377398).jpg?width=200 "Inheritance of dwarfing in maize. Demonstrating the heights of plants from the two parent variations and their F1 heterozygous hybrid (centre)")
![Hereditary defects in [[enzymes]] are generally inherited in an autosomal fashion because there are more non-X chromosomes than X-chromosomes, and a recessive fashion because the enzymes from the unaffected genes are generally sufficient to prevent symptoms in carriers. Exceptions include cases of [[haploinsufficiency]], where the unaffected gene cannot compensate for the affected one.](https://commons.wikimedia.org/wiki/Special:FilePath/Autosomal recessive inheritance for affected enzyme.png?width=200 "Hereditary defects in [[enzymes]] are generally inherited in an autosomal fashion because there are more non-X chromosomes than X-chromosomes, and a recessive fashion because the enzymes from the unaffected genes are generally sufficient to prevent symptoms in carriers. Exceptions include cases of [[haploinsufficiency]], where the unaffected gene cannot compensate for the affected one.")
![On the other hand, hereditary defects in structural proteins (such as [[osteogenesis imperfecta]], [[Marfan's syndrome]] and [[Ehlers–Danlos syndrome]]s) are generally autosomal dominant, because it is enough that some components are defective to make the whole structure dysfunctional. This is a dominant-negative process, wherein a mutated gene product adversely affects the non-mutated gene product within the same cell.](https://commons.wikimedia.org/wiki/Special:FilePath/Autosomal dominant inheritance for structural protein.png?width=200 "On the other hand, hereditary defects in structural proteins (such as [[osteogenesis imperfecta]], [[Marfan's syndrome]] and [[Ehlers–Danlos syndrome]]s) are generally autosomal dominant, because it is enough that some components are defective to make the whole structure dysfunctional. This is a dominant-negative process, wherein a mutated gene product adversely affects the non-mutated gene product within the same cell.")
INHERITANCE PATTERN OF A GENE
Incomplete dominance; Dominant gene; Dominance Relationships; Recessive allele; Recessive trait; Autosomal dominant; Autosomal recessive; Autosomal recessive trait; Codominance; Recessiveness; Dominant alleles; Co-dominant expression; Dominant trait; Dominant negative; Co-dominance; Dominant allele; Codominant; Recessive genes; Dominant genes; Co-dominant; Dominant carrier; Homozygous dominant; Homozygous recessive; Genes, dominant; Genes, recessive; Autosomal-dominant disease; Autosomal dominant inheritance; Recessive gene; Incomplete Dominance; Recessive refuge; Dominant disease; Recessive (genetics); Autosomal recessive gene; Recessive characteristic; Dominance Relationship; Genetic dominance; Evolution of dominance; Dominant characteristics; Dominance relationship; Recessivity; Recessively; Autosomal recessive disorder; Autosomal dominant disorder; Genetical dominance; Partial dominance; Partial Dominance; Co-Dominance; Semidominant; Autosomal Recessive; Semidominance; Semi-dominance; Partial dominence; Autorecessive; Double recessive; Incompletely dominant; Genetically recessive; Genetically dominant; Incomplete dominant; Recessive; Dominance (genetic); Principle of Dominance; Autosomal dominant disorders; Autosomal recessive inheritance; Autosomal co-dominant; Autosomal dominance; Dominant and recessive genes; Recessive and dominant genes; Complete dominance; Dominant and recessive; Dominance and recessiveness; Mendelian recessive disorder; Dominant (genetics); Dominant-negative mutation; Recessive inheritance
سِيادَةٌ مُشْتَرَكَة
