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MIR4453HG MIR4453 host gene [ Homo sapiens (human) ]

Gene ID: 54553, updated on 10-Oct-2023

Summary

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Official Symbol
MIR4453HGprovided by HGNC
Official Full Name
MIR4453 host geneprovided by HGNC
Primary source
HGNC:HGNC:25288
See related
Ensembl:ENSG00000268471 AllianceGenome:HGNC:25288
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
LINC02486; DKFZP434I0714
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Genomic context

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See MIR4453HG in Genome Data Viewer
Location:
4q31.3
Exon count:
1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 4 NC_000004.12 (152536264..152539263)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 4 NC_060928.1 (155859427..155862426)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 4 NC_000004.11 (153457416..153460415)

Chromosome 4 - NC_000004.12Genomic Context describing neighboring genes Neighboring gene F-box and WD repeat domain containing 7 Neighboring gene FBXW7 antisense RNA 1 Neighboring gene VISTA enhancer hs1361 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 22030 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 22031 Neighboring gene microRNA 3140 Neighboring gene ReSE screen-validated silencer GRCh37_chr4:153437089-153437307 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 22032 Neighboring gene H3K27ac hESC enhancer GRCh37_chr4:153456939-153457474 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 22034 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 22035 Neighboring gene microRNA 4453 Neighboring gene RPS3A pseudogene 18 Neighboring gene H3K27ac hESC enhancer GRCh37_chr4:153528082-153528582 Neighboring gene ribosomal protein S14 pseudogene 6

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. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Strausberg RL, et al. Proc Natl Acad Sci U S A, 2002 Dec 24. PMID 12477932, 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 studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

Genotypes

General gene information

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Markers

Other Names

  • long intergenic non-protein coding RNA 2486

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.

RNA

  1. NR_033797.2 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL137273
    Related
    ENST00000604157.1

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_000004.12 Reference GRCh38.p14 Primary Assembly

    Range
    152536264..152539263
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060928.1 Alternate T2T-CHM13v2.0

    Range
    155859427..155862426
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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