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MIR137 (microRNA 137)

Identity

Alias_namesMIRN137
Alias_symbol (synonym)hsa-mir-137
miR-137
Other alias
HGNC (Hugo) MIR137
LocusID (NCBI) 406928
Atlas_Id 50406
Location 1p21.3  [Link to chromosome band 1p21]
Location_base_pair Starts at 98046070 and ends at 98046171 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)MIR137   31523
Cards
Entrez_Gene (NCBI)MIR137  406928  microRNA 137
AliasesMIRN137; miR-137
GeneCards (Weizmann)MIR137
Ensembl hg19 (Hinxton)ENSG00000284202 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000284202 [Gene_View]  ENSG00000284202 [Sequence]  chr1:98046070-98046171 [Contig_View]  MIR137 [Vega]
ICGC DataPortalENSG00000284202
TCGA cBioPortalMIR137
AceView (NCBI)MIR137
Genatlas (Paris)MIR137
WikiGenes406928
SOURCE (Princeton)MIR137
Genetics Home Reference (NIH)MIR137
miRBaseMIR137
dbDEMCMIR137
Genomic and cartography
GoldenPath hg38 (UCSC)MIR137  -     chr1:98046070-98046171 -  1p21.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR137  -     1p21.3   [Description]    (hg19-Feb_2009)
GoldenPathMIR137 - 1p21.3 [CytoView hg19]  MIR137 - 1p21.3 [CytoView hg38]
ImmunoBaseENSG00000284202
Mapping of homologs : NCBIMIR137 [Mapview hg19]  MIR137 [Mapview hg38]
OMIM614304   
Gene and transcription
Genbank (Entrez)LM608494
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR137
Alternative Splicing GalleryENSG00000284202
Gene ExpressionMIR137 [ NCBI-GEO ]   MIR137 [ EBI - ARRAY_EXPRESS ]   MIR137 [ SEEK ]   MIR137 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR137 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)406928
GTEX Portal (Tissue expression)MIR137
Human Protein AtlasENSG00000284202-MIR137 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR137
DMDM Disease mutations406928
Blocks (Seattle)MIR137
Human Protein Atlas [tissue]ENSG00000284202-MIR137 [tissue]
Protein Interaction databases
FunCoupENSG00000284202
BioGRIDMIR137
STRING (EMBL)MIR137
ZODIACMIR137
Ontologies - Pathways
Huge Navigator MIR137 [HugePedia]
snp3D : Map Gene to Disease406928
BioCentury BCIQMIR137
ClinGenMIR137
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD406928
Chemical/Pharm GKB GenePA164722485
Clinical trialMIR137
Miscellaneous
canSAR (ICR)MIR137 (select the gene name)
DataMed IndexMIR137
Probes
Litterature
PubMed179 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR137
EVEXMIR137
GoPubMedMIR137
iHOPMIR137
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Aug 26 18:17:20 CEST 2019

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