Atlas of Genetics and Cytogenetics in Oncology and Haematology


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MIR5692C2 (microRNA 5692c-2)

Identity

Alias_symbol (synonym)hsa-mir-5692c-2
Other alias-
HGNC (Hugo) MIR5692C2
LocusID (NCBI) 100847017
Atlas_Id 69888
Location 10q24.2  [Link to chromosome band 10q24]
Location_base_pair Starts at 99354975 and ends at 99354995 bp from pter ( according to hg19-Feb_2009)

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)MIR5692C2   43448
Cards
Entrez_Gene (NCBI)MIR5692C2  100847017  microRNA 5692c-2
Aliases
GeneCards (Weizmann)MIR5692C2
Ensembl hg19 (Hinxton)ENSG00000266668 [Gene_View]  chr10:99354975-99354995 [Contig_View]  MIR5692C2 [Vega]
Ensembl hg38 (Hinxton)ENSG00000266668 [Gene_View]  chr10:99354975-99354995 [Contig_View]  MIR5692C2 [Vega]
ICGC DataPortalENSG00000266668
TCGA cBioPortalMIR5692C2
AceView (NCBI)MIR5692C2
Genatlas (Paris)MIR5692C2
WikiGenes100847017
SOURCE (Princeton)MIR5692C2
Genetics Home Reference (NIH)MIR5692C2
miRBaseMIR5692C2
dbDEMCMIR5692C2
Genomic and cartography
GoldenPath hg19 (UCSC)MIR5692C2  -     chr10:99354975-99354995 +  10q24.2   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR5692C2  -     10q24.2   [Description]    (hg38-Dec_2013)
EnsemblMIR5692C2 - 10q24.2 [CytoView hg19]  MIR5692C2 - 10q24.2 [CytoView hg38]
Mapping of homologs : NCBIMIR5692C2 [Mapview hg19]  MIR5692C2 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000007 NC_018918 NT_007933 NW_004929332
Consensus coding sequences : CCDS (NCBI)MIR5692C2
Alternative Splicing GalleryENSG00000266668
Gene ExpressionMIR5692C2 [ NCBI-GEO ]   MIR5692C2 [ EBI - ARRAY_EXPRESS ]   MIR5692C2 [ SEEK ]   MIR5692C2 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR5692C2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100847017
GTEX Portal (Tissue expression)MIR5692C2
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR5692C2
DMDM Disease mutations100847017
Blocks (Seattle)MIR5692C2
Human Protein AtlasENSG00000266668
Protein Interaction databases
FunCoupENSG00000266668
BioGRIDMIR5692C2
STRING (EMBL)MIR5692C2
ZODIACMIR5692C2
Ontologies - Pathways
Huge Navigator MIR5692C2 [HugePedia]
snp3D : Map Gene to Disease100847017
BioCentury BCIQMIR5692C2
ClinGenMIR5692C2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100847017
Clinical trialMIR5692C2
Miscellaneous
canSAR (ICR)MIR5692C2 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR5692C2
EVEXMIR5692C2
GoPubMedMIR5692C2
iHOPMIR5692C2
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 12:31:44 CET 2017

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