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MIR4792 microRNA 4792 [ Homo sapiens (human) ]

Gene ID: 100616448, discontinued on 14-Mar-2018
  • This record was discontinued.

Summary

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Official Symbol
MIR4792provided by HGNC
Official Full Name
microRNA 4792provided by HGNC
Primary source
HGNC:HGNC:41577
See related
miRBase:MI0017439
Gene type
ncRNA
RefSeq status
WITHDRAWN
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
miR-4792
Summary
This record was withdrawn by miRBase.
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Genomic context

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Location:
3p24.2
Exon count:
1
Annotation release Status Assembly Chr Location
105 latest, but not current GRCh37.p13 (GCF_000001405.25) 3 NC_000003.11 (24562853..24562926, complement)
105 latest, but not current HuRef (GCF_000002125.1) 3 AC_000135.1 (24508341..24508414, complement)
105 latest, but not current CHM1_1.1 (GCF_000306695.2) 3 NC_018914.2 (24514422..24514495, complement)

Genomic regions, transcripts, and products

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Genomic Sequence:
NC_000003.12 Chromosome 3 Reference GRCh38.p12 Primary Assembly

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?
  1. These findings suggest that miR-4792 functions as a tumor suppressor in NPC development and progression by targeting FOXC1.
    Title: miR-4792 inhibits epithelial-mesenchymal transition and invasion in nasopharyngeal carcinoma by targeting FOXC1.
  2. Data shsow that miR-363, miR-490, miR-137, miR-217 and miR-4792 were the top five significantly de-regulated miRNAs in uterine leiomyoma (ULM).
    Title: Characterization of the uterine leiomyoma microRNAome by deep sequencing.
Submit: New GeneRIF Correction

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

Genotypes

General gene information

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Other Names

  • hsa-mir-4792

NCBI Reference Sequences (RefSeq)

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RefSeqs of Annotated Genomes: Homo sapiens Annotation Release 109 (NOTE: not current)

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

Reference GRCh38.p12 Primary Assembly

Genomic

  1. NC_000003.12 Reference GRCh38.p12 Primary Assembly

    Range
    24521362..24521435 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. NR_039955.1 RNA Sequence

Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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