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MIR1-1HG MIR1-1 host gene [ Homo sapiens (human) ]

Gene ID: 128826, updated on 13-May-2022

Summary

Official Symbol
MIR1-1HGprovided by HGNC
Official Full Name
MIR1-1 host geneprovided by HGNC
Primary source
HGNC:HGNC:16159
See related
Ensembl:ENSG00000174407 AllianceGenome:HGNC:16159
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
C20orf166; MIR133A2HG
Expression
Biased expression in heart (RPKM 1.7), prostate (RPKM 1.3) and 3 other tissues See more
Orthologs
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Genomic context

See MIR1-1HG in Genome Data Viewer
Location:
20q13.33
Exon count:
4
Annotation release Status Assembly Chr Location
110 current GRCh38.p14 (GCF_000001405.40) 20 NC_000020.11 (62550453..62570764)
110 current T2T-CHM13v2.0 (GCF_009914755.1) 20 NC_060944.1 (64348970..64369291)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 20 NC_000020.10 (61147660..61167971)

Chromosome 20 - NC_000020.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124904947 Neighboring gene uncharacterized LOC105376995 Neighboring gene cardiomyocyte maturation associated lncRNA Neighboring gene microRNA 1-1 Neighboring gene microRNA 133a-2 Neighboring gene ribosomal protein L7 pseudogene 3 Neighboring gene long intergenic non-protein coding RNA 2970

Genomic regions, transcripts, and products

Expression

  • 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

General gene information

Markers

Homology

Other Names

  • MIR1-1 host gene protein
  • MIR133A2 host
  • uncharacterized protein C20orf166

Clone Names

  • FLJ32423, MGC129808

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_171007.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AL449263
    Related
    ENST00000624914.4

RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 110 details...Open this link in a new tab

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000020.11 Reference GRCh38.p14 Primary Assembly

    Range
    62550453..62570764
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060944.1 Alternate T2T-CHM13v2.0

    Range
    64348970..64369291
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001302812.2: Suppressed sequence

    Description
    NM_001302812.2: This RefSeq was removed because it is now thought that this gene does not encode a protein.
  2. NM_178463.4: Suppressed sequence

    Description
    NM_178463.4: This RefSeq was removed because it is now thought that this gene does not encode a protein.