Association of the SLC45A2 gene with physiological human hair colour variation (Q40044479)

16 September 2017

Association of the SLC45A2 gene with physiological human hair colour variation (English)

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16 September 2017

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1

Wojciech Branicki

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16 September 2017

5

Anna Wojas-Pelc

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16 September 2017

4

Tomasz Kupiec

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16 September 2017

3

Jolanta Draus-Barini

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16 September 2017

2

Urszula Brudnik

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16 September 2017

20 September 2008

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Journal of Human Genetics

16 September 2017

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16 September 2017

53

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16 September 2017

11-12

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16 September 2017

966-971

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https://scigraph.springernature.com/pub.10.1007/s10038-008-0338-3

16 September 2017

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Genetic determinants of hair, eye and skin pigmentation in Europeans

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Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expression

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Determination of phenotype associated SNPs in the MC1R gene.

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Sequences associated with human iris pigmentation.

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P gene mutations associated with oculocutaneous albinism type II (OCA2)

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Oculocutaneous albinism type 4 is one of the most common types of albinism in Japan

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Mutations in the MATP gene in five German patients affected by oculocutaneous albinism type 4

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Signatures of positive selection in genes associated with human skin pigmentation as revealed from analyses of single nucleotide polymorphisms.

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Genetics of Hair and Skin Color

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Evidence for recent positive selection at the human AIM1 locus in a European population.

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Two newly identified genetic determinants of pigmentation in Europeans

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Promoter polymorphisms in the MATP (SLC45A2) gene are associated with normal human skin color variation

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12 December 2020

The genetics of sun sensitivity in humans

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A three-single-nucleotide polymorphism haplotype in intron 1 of OCA2 explains most human eye-color variation

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Sequence polymorphism in the human melanocortin 1 receptor gene as an indicator of the red hair phenotype

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The 8818G allele of the agouti signaling protein (ASIP) gene is ancestral and is associated with darker skin color in African Americans.

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The contribution of melanocortin 1 receptor gene polymorphisms and the agouti signalling protein gene 8818A>G polymorphism to cutaneous melanoma and basal cell carcinoma in a Polish population.

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Novel MC1R variants in Ligurian melanoma patients and controls.

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Association of polymorphic sites in the OCA2 gene with eye colour using the tree scanning method.

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P gene as an inherited biomarker of human eye color.

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A polymorphism in the agouti signaling protein gene is associated with human pigmentation

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Genome-wide detection and characterization of positive selection in human populations

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The color loci of mice--a genetic century

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Tyrosinase processing and intracellular trafficking is disrupted in mouse primary melanocytes carrying the underwhite (uw) mutation. A model for oculocutaneous albinism (OCA) type 4.

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12 December 2020

Evidence for variable selective pressures at MC1R

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The future of association studies: gene-based analysis and replication

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Interaction between the melanocortin-1 receptor andP genes contributes to inter-individual variation in skin pigmentation phenotypes in a Tibetan population

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Population-based study of natural variation in the melanocortin-1 receptor gene and melanoma

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12 December 2020

SLC45A2: a novel malignant melanoma-associated gene

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12 December 2020

Non-replication of association studies: "pseudo-failures" to replicate?

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12 December 2020

MATP polymorphisms in Germans and Japanese: the L374F mutation as a population marker for Caucasoids

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12 December 2020

Distribution of the F374 Allele of the SLC45A2 (MATP) Gene and Founder-Haplotype Analysis

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12 December 2020

Single nucleotide polymorphisms in the MATP gene are associated with normal human pigmentation variation

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12 December 2020

A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation

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12 December 2020

10.1007/S10038-008-0338-3

Identifiers

DOI

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16 September 2017

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PubMed ID

18806926