Freckles

8K1715

Freckles are small, concentrated spots of melanin on the skin, often appearing on sun-exposed areas and becoming more prominent with sunlight exposure. Research shows that variations near genes involved in pigmentation regulation (like MC1R, TYR, and ASIP) strongly influence freckle formation and distribution. Freckl...

SNP Stats

Mapeados
15
Positivos
13 (86.7%)
Negativos
2 (13.3%)

Genome Matching (1)

Resultados Públicos (7.973)

Traços Conectados (1)

freckles

Freckles (EFO_0003963) are small, pigmented spots on the skin resulting from localized increases in melanin production, commonly influenced by UV exposure. They are strongly ass...

EFO_0003963

0 evidências22 SNPs1 traços0 estudos0 positivos · 0 negativos

Estudos Conectados (5)

Skin Phototype and Disease: A Comprehensive Genetic Approach to Pigmentary Traits Pleiotropy Using PRS in the GCAT Cohort.

PubMed 36672889

0 evidências284 SNPs5 traços1 estudos0 positivos · 0 negativos

Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations.

PubMed 29895819

0 evidências19 SNPs7 traços1 estudos0 positivos · 0 negativos

Web-based, participant-driven studies yield novel genetic associations for common traits.

PubMed 20585627

0 evidências18 SNPs6 traços1 estudos0 positivos · 0 negativos

Genes Conectados (5)

BNC2

basonuclin zinc finger protein 2

This gene encodes a conserved zinc finger protein. The encoded protein functions in skin color saturation. Mutations in this gene are associated with facial pigmented spots. Thi...

2 evidências297 SNPs0 traços0 estudos1 positivos · 1 negativos

HSPA12A

heat shock protein family A (Hsp70) member 12A

Predicted to enable ATP binding activity. Located in extracellular exosome. [provided by Alliance of Genome Resources, Apr 2022]

1 evidências36 SNPs0 traços0 estudos1 positivos · 0 negativos

SLC45A2

solute carrier family 45 member 2

This gene encodes a transporter protein that mediates melanin synthesis. The protein is expressed in a high percentage of melanoma cell lines. Mutations in this gene are a cause...

1 evidências29 SNPs0 traços0 estudos0 positivos · 1 negativos

TYR

tyrosinase

The enzyme encoded by this gene catalyzes the first 2 steps, and at least 1 subsequent step, in the conversion of tyrosine to melanin. The enzyme has both tyrosine hydroxylase a...

1 evidências28 SNPs0 traços0 estudos1 positivos · 0 negativos

EIF6

eukaryotic translation initiation factor 6

Hemidesmosomes are structures which link the basal lamina to the intermediate filament cytoskeleton. An important functional component of hemidesmosomes is the integrin beta-4 s...

1 evidências7 SNPs0 traços0 estudos1 positivos · 0 negativos

SNPs Conectados (15)

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