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MIR5095 microRNA 5095 [ Homo sapiens (human) ]

Gene ID: 100616458, discontinued on 14-Mar-2018
  • This record was discontinued.

Summary

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Official Symbol
MIR5095provided by HGNC
Official Full Name
microRNA 5095provided by HGNC
Primary source
HGNC:HGNC:41849
See related
miRBase:MI0018001
Gene type
ncRNA
RefSeq status
WITHDRAWN
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Summary
This record was withdrawn by miRBase.
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Genomic context

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Location:
1p32.3
Exon count:
1
Annotation release Status Assembly Chr Location
105 latest, but not current GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (53400602..53400689)
105 latest, but not current CHM1_1.1 (GCF_000306695.2) 1 NC_018912.2 (53517777..53517864)

Genomic regions, transcripts, and products

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Genomic Sequence:
NC_000001.11 Chromosome 1 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. SNHG7 promoted the proliferation, migration and invasion of glioblastoma cells through the inhibition of miR-5095 and concomitant activation of Wnt/beta-catenin signaling pathway.
    Title: Long noncoding RNA SNHG7 promotes the progression and growth of glioblastoma via inhibition of miR-5095.
  2. Groups of mRNAs in which the ordering of the miR-619-5p, miR-5095, miR-5096, and miR-5585-3p binding sites differ were established
    Title: The properties of binding sites of miR-619-5p, miR-5095, miR-5096, and miR-5585-3p in the mRNAs of human genes.
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-5095

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_000001.11 Reference GRCh38.p12 Primary Assembly

    Range
    52934930..52935017
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RNA

  1. NR_039970.1 RNA Sequence

Nucleotide Protein
Heading Accession and Version

Gene LinkOut

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