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MIR137HG MIR137 host gene [ Homo sapiens (human) ]

Gene ID: 400765, updated on 10-Oct-2023


Official Symbol
MIR137HGprovided by HGNC
Official Full Name
MIR137 host geneprovided by HGNC
Primary source
See related
Ensembl:ENSG00000225206 AllianceGenome:HGNC:42871
Gene type
RefSeq status
Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Low expression observed in reference dataset See more
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Genomic context

See MIR137HG in Genome Data Viewer
Exon count:
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (97988000..98049693, complement)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (97835839..97897607, complement)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (98453556..98515249, complement)

Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene long intergenic non-protein coding RNA 1930 Neighboring gene uncharacterized LOC124904227 Neighboring gene uncharacterized LOC124904228 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1110 Neighboring gene uncharacterized LOC124900404 Neighboring gene microRNA 2682 Neighboring gene microRNA 137 Neighboring gene NANOG hESC enhancer GRCh37_chr1:98552438-98552987 Neighboring gene NFU1 iron-sulfur cluster scaffold pseudogene 2 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:98670662-98671305 Neighboring gene long intergenic non-protein coding RNA 1776

Genomic regions, transcripts, and products


  • Project title: HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018


GeneRIFs: Gene References Into Functions

What's a GeneRIF?


EBI GWAS Catalog

Biological insights from 108 schizophrenia-associated genetic loci.
EBI GWAS Catalog
Genome wide association study (GWAS) of Chagas cardiomyopathy in Trypanosoma cruzi seropositive subjects.
EBI GWAS Catalog
Genome-wide association study identifies five new schizophrenia loci.
EBI GWAS Catalog
Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
EBI GWAS Catalog

General gene information

Other Names

  • MIR137 host gene (non-protein coding)

Clone Names

  • FLJ35409

Gene Ontology Provided by GOA

Process Evidence Code Pubs
involved_in miRNA-mediated post-transcriptional gene silencing IEA
Inferred from Electronic Annotation
more info
Component Evidence Code Pubs
part_of RISC complex IEA
Inferred from Electronic Annotation
more info

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.


  1. NR_046105.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AK094607, BX005019, DA791600

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


  1. NC_000001.11 Reference GRCh38.p14 Primary Assembly

    97988000..98049693 complement
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0


  1. NC_060925.1 Alternate T2T-CHM13v2.0

    97835839..97897607 complement
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001001688.1: Suppressed sequence

    NM_001001688.1: This RefSeq was permanently suppressed because currently there is support for the transcript but not for the protein.