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This is an accepted version of this page This is the latest accepted revision, reviewed on 28 December 2024. "Skin pigmentation" redirects here. For animal skin pigmentation, see Biological pigment. Extended Coloured family from South Africa showing some spectrum of human skin coloration Human skin color ranges from the darkest brown to the lightest hues. Differences in skin color among ...
Categorization of racial groups by reference to skin color is common in classical antiquity. [7] For example, it is found in e.g. Physiognomica, a Greek treatise dated to c. 300 BC. The transmission of the "color terminology" for race from antiquity to early anthropology in 17th century Europe took place via rabbinical literature.
Leucism (/ ˈ l uː s ɪ z əm,-k ɪ z-/) [2] [3] [4] is a wide variety of conditions that result in partial loss of pigmentation in an animal—causing white, pale, or patchy coloration of the skin, hair, feathers, scales, or cuticles, but not the eyes. [4] It is occasionally spelled leukism.
Genetic studies of traits and populations have been used to justify social inequalities associated with race, [7] despite the fact that patterns of human variation have been shown to be mostly clinal, [8] with human genetic code being approximately 99.6% – 99.9% identical between individuals and without clear boundaries between groups. [9] [10]
The euplotid nuclear code; The bacterial, archaeal and plant plastid code; The alternative yeast nuclear code; The ascidian mitochondrial code; The alternative flatworm mitochondrial code; The Blepharisma nuclear code [4] The chlorophycean mitochondrial code (none) (none) (none) (none) The trematode mitochondrial code; The Scenedesmus obliquus ...
In humans, a relatively small number of genes are thought to be responsible for human skin color. Different alleles or gene variants code for differences in the melanin found within the skin. Within some groups are high frequencies of dark skin alleles, while others have high frequencies of light skin alleles, for example.
Autosomal dominant A 50/50 chance of inheritance. Sickle-cell disease is inherited in the autosomal recessive pattern. When both parents have sickle-cell trait (carrier), a child has a 25% chance of sickle-cell disease (red icon), 25% do not carry any sickle-cell alleles (blue icon), and 50% have the heterozygous (carrier) condition. [1]
True white horses have unpigmented skin and hair due to the incomplete migration of melanocytes from the neural crest during development. [8] No health defects are associated with the cream gene. This is also true of the normal variations in skin, hair and eye color encoded on the human SLC45A2 gene. [9]