Genetics of hair and skin color
Abstract
Differences in skin and hair color are principally genetically determined and are due to variation in the amount, type, and packaging of melanin polymers produced by melanocytes secreted into keratinocytes. Pigmentary phenotype is genetically complex and at a physiological level complicated. Genes determining a number of rare Mendelian disorders of pigmentation such as albinism have been identified, but only one gene, the melanocortin 1 receptor (MCR1), has so far been identified to explain variation in the normal population such as that leading to red hair, freckling, and sun-sensitivity. Genotype-phenotype relations of the MC1R are reviewed, as well as methods to improve the phenotypic assessment of human pigmentary status. It is argued that given advances in model systems, increases in technical facility, and the lower cost of genotype assessment, the lack of standardized phenotype assessment is now a major limit on advance.
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Melanin is the major determining factor in intrinsic skin pigmentation.
“Melanin is the major determining factor in intrinsic skin pigmentation 43 ; therefore, we were most interested in identifying genes that affect melanin.”
From A Genomewide Association Study of Skin Pigmentation in a South Asian Population (2007) · cites this paper as [43]
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References 120 · Cited by 485
- Authors
- Rees, J. L.
- Affiliations
- University of Edinburgh (GB)
- Corresponding author
- Rees, Jonathan L.
- Venue
- Annual Review of Genetics
- Publisher
- Annual Reviews
- Published
- 2003-12
- Volume
- 37
- Issue
- 1
- Pages
- 67-90
- ISSN
- 0066-4197 (ISSN-L)
- 1545-2948
- OpenAlex
- W2112636438
- Cited by
- 485
- References
- 120
- Citations by year
- 2026: 12 · 2025: 5 · 2024: 13 · 2023: 8 · 2022: 16 · 2021: 31 · 2020: 13 · 2019: 16 · 2018: 15 · 2017: 27 · 2016: 20 · 2015: 21 · 2014: 24 · 2013: 32 · 2012: 15
- FWCI
- 1.37
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Annual Review of Genetics (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Wellcome Trust
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › melanin and skin pigmentation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Health Sciences › Medicine › Urology › Hair Growth and Disorders
- Keywords
- melanin, melanocytes, keratinocytes, MC1R, albinism, red hair, freckles, sun sensitivity, genotype-phenotype correlation
- MeSH terms
- alpha-MSH, Genotype, Hair Color, Humans, Melanins, Melanocytes, Phenotype, Skin Pigmentation, Structure-Activity Relationship, Genetic Variation, Intercellular Signaling Peptides and Proteins, Receptor, Melanocortin, Type 1, Agouti Signaling Protein
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