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LOC122861260 Sharpr-MPRA regulatory region 10987 [ Homo sapiens (human) ]

Gene ID: 122861260, updated on 10-Oct-2023

Summary

Gene symbol
LOC122861260
Gene description
Sharpr-MPRA regulatory region 10987
Gene type
biological region
Feature type(s)
regulatory: silencer
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 was predicted to be a transcriptional regulatory region based on chromatin state analysis from the ENCODE (ENCyclopedia Of DNA Elements) project. It was validated as a functional repressive element by the Sharpr-MPRA technique (Systematic high-resolution activation and repression profiling with reporter tiling using massively parallel reporter assays) in K562 erythroleukemia cells (group: K562 Repressive non-DNase unmatched - State 24:Quies, heterochromatin/dead zone). [provided by RefSeq, Oct 2021]
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Genomic context

See LOC122861260 in Genome Data Viewer
Location:
2q
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 2 NC_000002.12 (180607522..180607816)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 2 NC_060926.1 (181090952..181091246)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 2 NC_000002.11 (181472249..181472543)

Chromosome 2 - NC_000002.12Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105373769 Neighboring gene ReSE screen-validated silencer GRCh37_chr2:181293207-181293431 Neighboring gene uncharacterized LOC105373770 Neighboring gene ReSE screen-validated silencer GRCh37_chr2:181449937-181450113 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr2:181520993-181522192 Neighboring gene uncharacterized LOC105373771 Neighboring gene SWI/SNF complex antagonist associated with prostate cancer 1 Neighboring gene MPRA-validated peak3955 silencer Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr2:181678325-181679524 Neighboring gene ferritin heavy chain 1 pseudogene 20

Genomic regions, transcripts, and products

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_077076.1 

    Range
    101..395
    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_000002.12 Reference GRCh38.p14 Primary Assembly

    Range
    180607522..180607816
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060926.1 Alternate T2T-CHM13v2.0

    Range
    181090952..181091246
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)