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MIR7702 (microRNA 7702)

Identity

Alias_symbol (synonym)hsa-mir-7702
Other alias
HGNC (Hugo) MIR7702
LocusID (NCBI) 102465800
Atlas_Id 70234
Location 9q31.3  [Link to chromosome band 9q31]
Location_base_pair Starts at 114033436 and ends at 114033494 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)MIR7702   50216
Cards
Entrez_Gene (NCBI)MIR7702  102465800  microRNA 7702
Aliaseshsa-mir-7702
GeneCards (Weizmann)MIR7702
Ensembl hg19 (Hinxton)ENSG00000274263 [Gene_View]  chr9:114033436-114033494 [Contig_View]  MIR7702 [Vega]
Ensembl hg38 (Hinxton)ENSG00000274263 [Gene_View]  chr9:114033436-114033494 [Contig_View]  MIR7702 [Vega]
ICGC DataPortalENSG00000274263
TCGA cBioPortalMIR7702
AceView (NCBI)MIR7702
Genatlas (Paris)MIR7702
WikiGenes102465800
SOURCE (Princeton)MIR7702
Genetics Home Reference (NIH)MIR7702
miRBaseMIR7702
dbDEMCMIR7702
Genomic and cartography
GoldenPath hg19 (UCSC)MIR7702  -     chr9:114033436-114033494 -  9q31.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR7702  -     9q31.3   [Description]    (hg38-Dec_2013)
EnsemblMIR7702 - 9q31.3 [CytoView hg19]  MIR7702 - 9q31.3 [CytoView hg38]
Mapping of homologs : NCBIMIR7702 [Mapview hg19]  MIR7702 [Mapview hg38]
Gene and transcription
Genbank (Entrez)KC832799
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000009 NC_018920 NT_008470 NW_004929366
Consensus coding sequences : CCDS (NCBI)MIR7702
Alternative Splicing GalleryENSG00000274263
Gene ExpressionMIR7702 [ NCBI-GEO ]   MIR7702 [ EBI - ARRAY_EXPRESS ]   MIR7702 [ SEEK ]   MIR7702 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR7702 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)102465800
GTEX Portal (Tissue expression)MIR7702
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR7702
DMDM Disease mutations102465800
Blocks (Seattle)MIR7702
Human Protein AtlasENSG00000274263
Protein Interaction databases
FunCoupENSG00000274263
BioGRIDMIR7702
STRING (EMBL)MIR7702
ZODIACMIR7702
Ontologies - Pathways
Huge Navigator MIR7702 [HugePedia]
snp3D : Map Gene to Disease102465800
BioCentury BCIQMIR7702
ClinGenMIR7702
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD102465800
Clinical trialMIR7702
Miscellaneous
canSAR (ICR)MIR7702 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR7702
EVEXMIR7702
GoPubMedMIR7702
iHOPMIR7702
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 : Tue Mar 14 12:32:57 CET 2017

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