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MIR4697HG MIR4697 host gene [ Homo sapiens (human) ]

Gene ID: 283174, updated on 10-Dec-2019

Summary

Official Symbol
MIR4697HGprovided by HGNC
Official Full Name
MIR4697 host geneprovided by HGNC
Primary source
HGNC:HGNC:27448
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
LINC00947

Genomic context

See MIR4697HG in Genome Data Viewer
Location:
11q25
Exon count:
1
Annotation release Status Assembly Chr Location
109.20191205 current GRCh38.p13 (GCF_000001405.39) 11 NC_000011.10 (133896435..133901740, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (133766330..133771635, complement)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene spermatogenesis associated 19 Neighboring gene calponin 2 pseudogene Neighboring gene microRNA 4697 Neighboring gene immunoglobulin superfamily member 9B Neighboring gene long intergenic non-protein coding RNA 2730

Genomic regions, transcripts, and products

General gene information

Markers

Other Names

  • MIR4697 host gene (non-protein coding)
  • long intergenic non-protein coding RNA 947

Clone Names

  • MGC117185, MGC126740

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_024344.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AP001979

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.

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

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000011.10 Reference GRCh38.p13 Primary Assembly

    Range
    133896435..133901740 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001001873.3: Suppressed sequence

    Description
    NM_001001873.3: This RefSeq was permanently suppressed because currently there is support for the transcript but not for the protein.
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