Atlas of Genetics and Cytogenetics in Oncology and Haematology


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MIR5692A1 (microRNA 5692a-1)

Identity

Alias_symbol (synonym)hsa-mir-5692a-1
Other alias-
HGNC (Hugo) MIR5692A1
LocusID (NCBI) 100847066
Atlas_Id 69885
Location 7q21.3  [Link to chromosome band 7q21]
Location_base_pair Starts at 97963658 and ends at 97963726 bp from pter ( according to hg38-Dec_2013)

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)MIR5692A1   43533
Cards
Entrez_Gene (NCBI)MIR5692A1  100847066  microRNA 5692a-1
Aliases
GeneCards (Weizmann)MIR5692A1
Ensembl hg19 (Hinxton)ENSG00000266318 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000266318 [Gene_View]  chr7:97963658-97963726 [Contig_View]  MIR5692A1 [Vega]
ICGC DataPortalENSG00000266318
TCGA cBioPortalMIR5692A1
AceView (NCBI)MIR5692A1
Genatlas (Paris)MIR5692A1
WikiGenes100847066
SOURCE (Princeton)MIR5692A1
Genetics Home Reference (NIH)MIR5692A1
miRBaseMIR5692A1
dbDEMCMIR5692A1
Genomic and cartography
GoldenPath hg38 (UCSC)MIR5692A1  -     chr7:97963658-97963726 +  7q21.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR5692A1  -     7q21.3   [Description]    (hg19-Feb_2009)
EnsemblMIR5692A1 - 7q21.3 [CytoView hg19]  MIR5692A1 - 7q21.3 [CytoView hg38]
Mapping of homologs : NCBIMIR5692A1 [Mapview hg19]  MIR5692A1 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR5692A1
Alternative Splicing GalleryENSG00000266318
Gene ExpressionMIR5692A1 [ NCBI-GEO ]   MIR5692A1 [ EBI - ARRAY_EXPRESS ]   MIR5692A1 [ SEEK ]   MIR5692A1 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR5692A1 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100847066
GTEX Portal (Tissue expression)MIR5692A1
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR5692A1
DMDM Disease mutations100847066
Blocks (Seattle)MIR5692A1
Human Protein AtlasENSG00000266318
Protein Interaction databases
FunCoupENSG00000266318
BioGRIDMIR5692A1
STRING (EMBL)MIR5692A1
ZODIACMIR5692A1
Ontologies - Pathways
Huge Navigator MIR5692A1 [HugePedia]
snp3D : Map Gene to Disease100847066
BioCentury BCIQMIR5692A1
ClinGenMIR5692A1
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100847066
Clinical trialMIR5692A1
Miscellaneous
canSAR (ICR)MIR5692A1 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR5692A1
EVEXMIR5692A1
GoPubMedMIR5692A1
iHOPMIR5692A1
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

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indexed on : Mon Sep 18 13:29:49 CEST 2017

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