U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

MIR4300HG MIR4300 host gene [ Homo sapiens (human) ]

Gene ID: 101928989, updated on 17-Sep-2024

Summary

Go to the top of the page Help
Official Symbol
MIR4300HGprovided by HGNC
Official Full Name
MIR4300 host geneprovided by HGNC
Primary source
HGNC:HGNC:52003
See related
Ensembl:ENSG00000245832 AllianceGenome:HGNC:52003
Gene type
ncRNA
RefSeq status
VALIDATED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Expression
Low expression observed in reference dataset See more
NEW
Try the new Gene table
Try the new Transcript table

Genomic context

Go to the top of the page Help
See MIR4300HG in Genome Data Viewer
Location:
11q14.1
Exon count:
8
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 11 NC_000011.10 (81879851..82403913, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 11 NC_060935.1 (81814629..82339983, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 11 NC_000011.9 (81590893..82114955, complement)

Chromosome 11 - NC_000011.10Genomic Context describing neighboring genes Neighboring gene MT-ND6 pseudogene 25 Neighboring gene MT-CYB pseudogene 25 Neighboring gene OCT4-NANOG-H3K4me1 hESC enhancer GRCh37_chr11:81358275-81358976 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:81358977-81359677 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 5331 Neighboring gene microRNA 4300 Neighboring gene P300/CBP strongly-dependent group 1 enhancer GRCh37_chr11:81714171-81715370 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr11:81736281-81736824 Neighboring gene uncharacterized LOC105369410 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr11:82364504-82365004 Neighboring gene MPRA-validated peak1371 silencer Neighboring gene Sharpr-MPRA regulatory region 11396 Neighboring gene ribosomal protein S28 pseudogene 7

Genomic regions, transcripts, and products

Go to the top of the page Help

Go to nucleotide: Graphics FASTA GenBank

Expression

Go to the top of the page Help
  • Project title: HPA RNA-seq normal tissues 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

Bibliography

Go to the top of the pageHelp

Related articles in PubMed

  1. Genetic variant of MIR4300HG is associated with progression of adolescent idiopathic scoliosis in a Chinese population. Wang Y, et al. J Orthop Surg Res, 2021 May 13. PMID 33985553, Free PMC Article
  2. Long non-coding RNA MIR4300HG polymorphisms are associated with postoperative nausea and vomiting: a genome-wide association study. Sugino S, et al. Hum Genomics, 2020 Sep 14. PMID 32928300, Free PMC Article
  3. 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

What's a GeneRIF?
  1. Long non-coding RNA MIR4300HG polymorphisms are associated with postoperative nausea and vomiting: a genome-wide association study.
    Title: Long non-coding RNA MIR4300HG polymorphisms are associated with postoperative nausea and vomiting: a genome-wide association study.
  2. Genetic variant of MIR4300HG is associated with progression of adolescent idiopathic scoliosis in a Chinese population.
    Title: Genetic variant of MIR4300HG is associated with progression of adolescent idiopathic scoliosis in a Chinese population.
Submit: New GeneRIF Correction

Phenotypes

Go to the top of the page Help

Review eQTL and phenotype association data in this region using PheGenI

Variation

Go to the top of the page Help

See Variation Viewer (GRCh37.p13)

NCBI Reference Sequences (RefSeq)

Go to the top of the page Help

NEW Try the new Transcript table

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_120571.1 RNA Sequence

    Status: VALIDATED

    Source sequence(s)
    AI149635, AP003060, BC041900
    Related
    ENST00000500502.5

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

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

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000011.10 Reference GRCh38.p14 Primary Assembly

    Range
    81879851..82403913 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060935.1 Alternate T2T-CHM13v2.0

    Range
    81814629..82339983 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

Gene LinkOut

The following LinkOut resources are supplied by external providers. These providers are responsible for maintaining the links.

Molecular Biology Databases
Research Materials