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LOC128781591 melanoma risk locus-associated MPRA allelic enhancers 9:12675264 and 9:12675284 [ Homo sapiens (human) ]

Gene ID: 128781591, updated on 10-Oct-2023

Summary

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Gene symbol
LOC128781591
Gene description
melanoma risk locus-associated MPRA allelic enhancers 9:12675264 and 9:12675284
Gene type
biological region
Feature type(s)
regulatory: enhancer, transcriptional_cis_regulatory_region
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Summary
This genomic sequence includes two genetic variants, rs10960751 and rs10960752, that are in strong linkage disequilibrium with a melanoma risk locus identified at 9p23 in genome-wide association studies (GWASs), and for which the reference alleles have protective effects. Two overlapping subregions were validated as functional enhancers by massively parallel reporter assays (MPRAs) in C283T melanocytes and UACC903 melanoma cells, where differences in transcriptional activity were observed between the reference and alternative alleles for both variants. [provided by RefSeq, Mar 2023]
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Genomic context

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Location:
chromosome: 9
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (12675192..12675356)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (12684546..12684710)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene JNK1/MAPK8-associated membrane protein pseudogene 1 Neighboring gene RNA, U2 small nuclear 47, pseudogene Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr9:12334327-12334960 Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:12438630-12439130 Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:12439131-12439631 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr9:12440846-12441628 Neighboring gene H3K27ac hESC enhancer GRCh37_chr9:12463247-12463746 Neighboring gene melanoma risk locus-associated MPRA allelic enhancer 9:12581404 Neighboring gene melanoma risk locus-associated MPRA allelic enhancer 9:12636264 Neighboring gene melanoma risk locus-associated MPRA allelic enhancer 9:12651340 Neighboring gene melanoma risk locus-associated MPRA allelic enhancer 9:12660541 Neighboring gene melanoma risk locus-associated MPRA allelic enhancer 9:12671566 Neighboring gene LURAP1L antisense RNA 1 Neighboring gene tyrosinase related protein 1 Neighboring gene RNA, 7SL, cytoplasmic 849, pseudogene

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. Massively parallel reporter assays and variant scoring identified functional variants and target genes for melanoma loci and highlighted cell-type specificity. Long E, et al. Am J Hum Genet, 2022 Dec 1. PMID 36423637, Free PMC Article
  2. Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility. Landi MT, et al. Nat Genet, 2020 May. PMID 32341527, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See variants in ClinVar

General gene information

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Other Names

  • melanoma risk locus-associated MPRA allelic enhancer 9:12675264
  • melanoma risk locus-associated MPRA allelic enhancer 9:12675284

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

  1. NG_149941.1 

    Range
    101..265
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000009.12 Reference GRCh38.p14 Primary Assembly

    Range
    12675192..12675356
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    12684546..12684710
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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