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MIR7705 (microRNA 7705)

Identity

Alias_symbol (synonym)hsa-mir-7705
Other alias
HGNC (Hugo) MIR7705
LocusID (NCBI) 102466854
Atlas_Id 70236
Location 8q22.3  [Link to chromosome band 8q22]
Location_base_pair Starts at 101715196 and ends at 101715252 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)MIR7705   50143
Cards
Entrez_Gene (NCBI)MIR7705  102466854  microRNA 7705
Aliaseshsa-mir-7705
GeneCards (Weizmann)MIR7705
Ensembl hg19 (Hinxton)ENSG00000277719 [Gene_View]  chr8:101715196-101715252 [Contig_View]  MIR7705 [Vega]
Ensembl hg38 (Hinxton)ENSG00000277719 [Gene_View]  chr8:101715196-101715252 [Contig_View]  MIR7705 [Vega]
ICGC DataPortalENSG00000277719
TCGA cBioPortalMIR7705
AceView (NCBI)MIR7705
Genatlas (Paris)MIR7705
WikiGenes102466854
SOURCE (Princeton)MIR7705
Genetics Home Reference (NIH)MIR7705
miRBaseMIR7705
dbDEMCMIR7705
Genomic and cartography
GoldenPath hg19 (UCSC)MIR7705  -     chr8:101715196-101715252 -  8q22.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR7705  -     8q22.3   [Description]    (hg38-Dec_2013)
EnsemblMIR7705 - 8q22.3 [CytoView hg19]  MIR7705 - 8q22.3 [CytoView hg38]
Mapping of homologs : NCBIMIR7705 [Mapview hg19]  MIR7705 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000008 NC_018919 NT_008046 NW_004929340
Consensus coding sequences : CCDS (NCBI)MIR7705
Alternative Splicing GalleryENSG00000277719
Gene ExpressionMIR7705 [ NCBI-GEO ]   MIR7705 [ EBI - ARRAY_EXPRESS ]   MIR7705 [ SEEK ]   MIR7705 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR7705 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)102466854
GTEX Portal (Tissue expression)MIR7705
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR7705
DMDM Disease mutations102466854
Blocks (Seattle)MIR7705
Human Protein AtlasENSG00000277719
Protein Interaction databases
FunCoupENSG00000277719
BioGRIDMIR7705
STRING (EMBL)MIR7705
ZODIACMIR7705
Ontologies - Pathways
Huge Navigator MIR7705 [HugePedia]
snp3D : Map Gene to Disease102466854
BioCentury BCIQMIR7705
ClinGenMIR7705
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD102466854
Clinical trialMIR7705
Miscellaneous
canSAR (ICR)MIR7705 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR7705
EVEXMIR7705
GoPubMedMIR7705
iHOPMIR7705
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 12:32:58 CET 2017

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