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LOC110120816 VISTA enhancer hs974 [ Homo sapiens (human) ]

Gene ID: 110120816, updated on 10-Oct-2023

Summary

Gene symbol
LOC110120816
Gene description
VISTA enhancer hs974
Gene type
biological region
Feature type(s)
regulatory: enhancer
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Summary
This locus represents a conserved genomic element that can function as an enhancer. It can activate a Hsp68 promoter coupled to a LacZ reporter gene in transgenic mice embryos. A subregion associated with the NANOG transcription factor was also shown to be an active enhancer by ChIP-STARR-seq in naive human embryonic stem cells. [provided by RefSeq, Nov 2022]
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Genomic context

Location:
chromosome: 9
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 9 NC_000009.12 (80797785..80799057)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 9 NC_060933.1 (92949644..92950919)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 9 NC_000009.11 (83412700..83413972)

Chromosome 9 - NC_000009.12Genomic Context describing neighboring genes Neighboring gene MT-ND2 pseudogene 9 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr9:83236200-83236732 Neighboring gene NANOG hESC enhancer GRCh37_chr9:83279636-83280146 Neighboring gene ribosomal protein S19 pseudogene 6 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr9:83450894-83452093 Neighboring gene uncharacterized LOC107987085 Neighboring gene uncharacterized LOC107987084

Genomic regions, transcripts, and products

General gene information

Other Names

  • NANOG hESC enhancer GRCh37_chr9:83413123-83413634

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_053441.1 

    Range
    101..1373
    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
    80797785..80799057
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    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060933.1 Alternate T2T-CHM13v2.0

    Range
    92949644..92950919
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)