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LOC110120857 VISTA enhancer hs348 [ Homo sapiens (human) ]

Gene ID: 110120857, updated on 10-Oct-2023

Summary

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Gene symbol
LOC110120857
Gene description
VISTA enhancer hs348
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: 14
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 14 NC_000014.9 (35550818..35551792)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 14 NC_060938.1 (29738544..29739518)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 14 NC_000014.8 (36020024..36020998)

Chromosome 14 - NC_000014.9Genomic Context describing neighboring genes Neighboring gene keratin 18 pseudogene 6 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr14:36002164-36002988 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:36002989-36003812 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:36003813-36004636 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr14:36004637-36005459 Neighboring gene Ral GTPase activating protein catalytic subunit alpha 1 Neighboring gene INSM transcriptional repressor 2 Neighboring gene uncharacterized LOC124900348 Neighboring gene small nucleolar RNA, H/ACA box 101B

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_053480.1 

    Range
    101..1075
    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_000014.9 Reference GRCh38.p14 Primary Assembly

    Range
    35550818..35551792
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060938.1 Alternate T2T-CHM13v2.0

    Range
    29738544..29739518
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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