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MIR4453HG MIR4453 host gene [ Homo sapiens (human) ]

Gene ID: 54553, updated on 10-Oct-2019

Summary

Official Symbol
MIR4453HGprovided by HGNC
Official Full Name
MIR4453 host geneprovided by HGNC
Primary source
HGNC:HGNC:25288
See related
Ensembl:ENSG00000268471
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

Genomic context

See MIR4453HG in Genome Data Viewer
Location:
4q31.3
Exon count:
1
Annotation release Status Assembly Chr Location
109.20190905 current GRCh38.p13 (GCF_000001405.39) 4 NC_000004.12 (152536264..152539263)
105 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 VISTA enhancer hs1361 Neighboring gene microRNA 3140 Neighboring gene microRNA 4453 Neighboring gene RPS3A pseudogene 18 Neighboring gene ribosomal protein S14 pseudogene 6

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • long intergenic non-protein coding RNA 2486

NCBI Reference Sequences (RefSeq)

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: Homo sapiens Annotation Release 109.20190905

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000004.12 Reference GRCh38.p13 Primary Assembly

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