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MIR567 (microRNA 567)

Identity

Alias (NCBI)MIRN567
hsa-mir-567
HGNC (Hugo) MIR567
HGNC Alias symbhsa-mir-567
HGNC Previous nameMIRN567
LocusID (NCBI) 693152
Atlas_Id 58073
Location 3q13.2  [Link to chromosome band 3q13]
Location_base_pair Starts at 112112801 and ends at 112112898 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

Note

Non-annotated gene. Preliminary data : if you are an author
who wish to write a full paper/card on this gene, go to  How to contribute

DNA/RNA

 



External links

Nomenclature
HGNC (Hugo)MIR567   32823
Cards
Entrez_Gene (NCBI)MIR567  693152  microRNA 567
AliasesMIRN567; hsa-mir-567
GeneCards (Weizmann)MIR567
Ensembl hg19 (Hinxton)ENSG00000207940 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000207940 [Gene_View]  ENSG00000207940 [Sequence]  chr3:112112801-112112898 [Contig_View]  MIR567 [Vega]
ICGC DataPortalENSG00000207940
TCGA cBioPortalMIR567
AceView (NCBI)MIR567
Genatlas (Paris)MIR567
WikiGenes693152
SOURCE (Princeton)MIR567
Genetics Home Reference (NIH)MIR567
miRBaseMIR567
dbDEMCMIR567
Genomic and cartography
GoldenPath hg38 (UCSC)MIR567  -     chr3:112112801-112112898 +  3q13.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR567  -     3q13.2   [Description]    (hg19-Feb_2009)
GoldenPathMIR567 - 3q13.2 [CytoView hg19]  MIR567 - 3q13.2 [CytoView hg38]
ImmunoBaseENSG00000207940
genome Data Viewer NCBIMIR567 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR567
Alternative Splicing GalleryENSG00000207940
Gene ExpressionMIR567 [ NCBI-GEO ]   MIR567 [ EBI - ARRAY_EXPRESS ]   MIR567 [ SEEK ]   MIR567 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR567 [ Firebrowse - Broad ]
GenevisibleExpression of MIR567 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)693152
GTEX Portal (Tissue expression)MIR567
Human Protein AtlasENSG00000207940-MIR567 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR567
DMDM Disease mutations693152
Blocks (Seattle)MIR567
Human Protein Atlas [tissue]ENSG00000207940-MIR567 [tissue]
Protein Interaction databases
FunCoupENSG00000207940
BioGRIDMIR567
STRING (EMBL)MIR567
ZODIACMIR567
Ontologies - Pathways
Huge Navigator MIR567 [HugePedia]
snp3D : Map Gene to Disease693152
BioCentury BCIQMIR567
ClinGenMIR567
Clinical trials, drugs, therapy
Protein Interactions : CTD693152
Pharm GKB GenePA164722864
Clinical trialMIR567
Miscellaneous
canSAR (ICR)MIR567 (select the gene name)
HarmonizomeMIR567
DataMed IndexMIR567
Probes
Litterature
PubMed5 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR567
EVEXMIR567
GoPubMedMIR567
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Sep 14 14:21:57 CEST 2020

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