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MIR4692 (microRNA 4692)

Identity

Alias_symbol (synonym)hsa-mir-4692
Other alias-
HGNC (Hugo) MIR4692
LocusID (NCBI) 100616410
Atlas_Id 69607
Location 11q13.4  [Link to chromosome band 11q13]
Location_base_pair Starts at 72783530 and ends at 72783592 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)MIR4692   41856
Cards
Entrez_Gene (NCBI)MIR4692  100616410  microRNA 4692
Aliases
GeneCards (Weizmann)MIR4692
Ensembl hg19 (Hinxton)ENSG00000265064 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000265064 [Gene_View]  chr11:72783530-72783592 [Contig_View]  MIR4692 [Vega]
ICGC DataPortalENSG00000265064
TCGA cBioPortalMIR4692
AceView (NCBI)MIR4692
Genatlas (Paris)MIR4692
WikiGenes100616410
SOURCE (Princeton)MIR4692
Genetics Home Reference (NIH)MIR4692
miRBaseMIR4692
dbDEMCMIR4692
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4692  -     chr11:72783530-72783592 +  11q13.4   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4692  -     11q13.4   [Description]    (hg19-Feb_2009)
EnsemblMIR4692 - 11q13.4 [CytoView hg19]  MIR4692 - 11q13.4 [CytoView hg38]
Mapping of homologs : NCBIMIR4692 [Mapview hg19]  MIR4692 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4692
Alternative Splicing GalleryENSG00000265064
Gene ExpressionMIR4692 [ NCBI-GEO ]   MIR4692 [ EBI - ARRAY_EXPRESS ]   MIR4692 [ SEEK ]   MIR4692 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4692 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616410
GTEX Portal (Tissue expression)MIR4692
Human Protein AtlasENSG00000265064-MIR4692 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4692
DMDM Disease mutations100616410
Blocks (Seattle)MIR4692
Human Protein Atlas [tissue]ENSG00000265064-MIR4692 [tissue]
Protein Interaction databases
FunCoupENSG00000265064
BioGRIDMIR4692
STRING (EMBL)MIR4692
ZODIACMIR4692
Ontologies - Pathways
Huge Navigator MIR4692 [HugePedia]
snp3D : Map Gene to Disease100616410
BioCentury BCIQMIR4692
ClinGenMIR4692
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616410
Clinical trialMIR4692
Miscellaneous
canSAR (ICR)MIR4692 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4692
EVEXMIR4692
GoPubMedMIR4692
iHOPMIR4692
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and haemadožogy
indexed on : Thu Nov 9 12:15:03 CET 2017

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