Atlas of Genetics and Cytogenetics in Oncology and Haematology


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MIR3692 (microRNA 3692)

Identity

Alias (NCBI)-
HGNC (Hugo) MIR3692
HGNC Alias symbhsa-mir-3692
LocusID (NCBI) 100500899
Atlas_Id 69300
Location 6q25.3  [Link to chromosome band 6q25]
Location_base_pair Starts at 157529132 and ends at 157529200 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)MIR3692   38885
Cards
Entrez_Gene (NCBI)MIR3692  100500899  microRNA 3692
Aliases
GeneCards (Weizmann)MIR3692
Ensembl hg19 (Hinxton)ENSG00000266617 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000266617 [Gene_View]  ENSG00000266617 [Sequence]  chr6:157529132-157529200 [Contig_View]  MIR3692 [Vega]
ICGC DataPortalENSG00000266617
TCGA cBioPortalMIR3692
AceView (NCBI)MIR3692
Genatlas (Paris)MIR3692
WikiGenes100500899
SOURCE (Princeton)MIR3692
Genetics Home Reference (NIH)MIR3692
miRBaseMIR3692
dbDEMCMIR3692
Genomic and cartography
GoldenPath hg38 (UCSC)MIR3692  -     chr6:157529132-157529200 +  6q25.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR3692  -     6q25.3   [Description]    (hg19-Feb_2009)
GoldenPathMIR3692 - 6q25.3 [CytoView hg19]  MIR3692 - 6q25.3 [CytoView hg38]
ImmunoBaseENSG00000266617
genome Data Viewer NCBIMIR3692 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR3692
Alternative Splicing GalleryENSG00000266617
Gene ExpressionMIR3692 [ NCBI-GEO ]   MIR3692 [ EBI - ARRAY_EXPRESS ]   MIR3692 [ SEEK ]   MIR3692 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR3692 [ Firebrowse - Broad ]
GenevisibleExpression of MIR3692 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100500899
GTEX Portal (Tissue expression)MIR3692
Human Protein AtlasENSG00000266617-MIR3692 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR3692
DMDM Disease mutations100500899
Blocks (Seattle)MIR3692
Human Protein Atlas [tissue]ENSG00000266617-MIR3692 [tissue]
Protein Interaction databases
FunCoupENSG00000266617
BioGRIDMIR3692
STRING (EMBL)MIR3692
ZODIACMIR3692
Ontologies - Pathways
Huge Navigator MIR3692 [HugePedia]
snp3D : Map Gene to Disease100500899
BioCentury BCIQMIR3692
ClinGenMIR3692
Clinical trials, drugs, therapy
Protein Interactions : CTD100500899
Clinical trialMIR3692
Miscellaneous
canSAR (ICR)MIR3692 (select the gene name)
HarmonizomeMIR3692
DataMed IndexMIR3692
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR3692
EVEXMIR3692
GoPubMedMIR3692
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Sat Aug 22 19:25:27 CEST 2020

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