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LOC110121373 VISTA enhancer hs1467 [ Homo sapiens (human) ]

Gene ID: 110121373, updated on 10-Oct-2023

Summary

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Gene symbol
LOC110121373
Gene description
VISTA enhancer hs1467
Gene type
biological region
Feature type(s)
regulatory: enhancer
RefSeq status
PROVISIONAL
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. [provided by RefSeq, Jun 2015]
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Genomic context

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Location:
chromosome: 17
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 17 NC_000017.11 (71003328..71004627)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 17 NC_060941.1 (71876009..71877308)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (68999469..69000768)

Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC105371884 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr17:68859717-68860916 Neighboring gene NANOG hESC enhancer GRCh37_chr17:68865615-68866532 Neighboring gene uncharacterized LOC124904104 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr17:68983705-68984206 Neighboring gene SERPINE1 mRNA binding protein 1 pseudogene Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr17:69028546-69029302 Neighboring gene SOX9 enhancer cre1 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr17:69029303-69030057 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr17:69067578-69068777 Neighboring gene enhancer upstream of SOX9 Neighboring gene cancer susceptibility 17

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. VISTA Enhancer Browser--a database of tissue-specific human enhancers. Visel A, et al. Nucleic Acids Res, 2007 Jan. PMID 17130149, 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

See Variation Viewer (GRCh37.p13)

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_053987.1 

    Range
    101..1400
    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_000017.11 Reference GRCh38.p14 Primary Assembly

    Range
    71003328..71004627
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060941.1 Alternate T2T-CHM13v2.0

    Range
    71876009..71877308
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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