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MIR4770 (microRNA 4770)

Identity

Alias_symbol (synonym)hsa-mir-4770
Other alias-
HGNC (Hugo) MIR4770
LocusID (NCBI) 100616373
Atlas_Id 69683
Location Xp22.31  [Link to chromosome band Xp22]
Location_base_pair Starts at 6383906 and ends at 6383963 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)MIR4770   41542
Cards
Entrez_Gene (NCBI)MIR4770  100616373  microRNA 4770
Aliases
GeneCards (Weizmann)MIR4770
Ensembl hg19 (Hinxton)ENSG00000265284 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000265284 [Gene_View]  chrX:6383906-6383963 [Contig_View]  MIR4770 [Vega]
ICGC DataPortalENSG00000265284
TCGA cBioPortalMIR4770
AceView (NCBI)MIR4770
Genatlas (Paris)MIR4770
WikiGenes100616373
SOURCE (Princeton)MIR4770
Genetics Home Reference (NIH)MIR4770
miRBaseMIR4770
dbDEMCMIR4770
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4770  -     chrX:6383906-6383963 -  Xp22.31   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4770  -     Xp22.31   [Description]    (hg19-Feb_2009)
EnsemblMIR4770 - Xp22.31 [CytoView hg19]  MIR4770 - Xp22.31 [CytoView hg38]
Mapping of homologs : NCBIMIR4770 [Mapview hg19]  MIR4770 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4770
Alternative Splicing GalleryENSG00000265284
Gene ExpressionMIR4770 [ NCBI-GEO ]   MIR4770 [ EBI - ARRAY_EXPRESS ]   MIR4770 [ SEEK ]   MIR4770 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4770 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616373
GTEX Portal (Tissue expression)MIR4770
Human Protein AtlasENSG00000265284-MIR4770 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4770
DMDM Disease mutations100616373
Blocks (Seattle)MIR4770
Human Protein Atlas [tissue]ENSG00000265284-MIR4770 [tissue]
Protein Interaction databases
FunCoupENSG00000265284
BioGRIDMIR4770
STRING (EMBL)MIR4770
ZODIACMIR4770
Ontologies - Pathways
Huge Navigator MIR4770 [HugePedia]
snp3D : Map Gene to Disease100616373
BioCentury BCIQMIR4770
ClinGenMIR4770
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616373
Clinical trialMIR4770
Miscellaneous
canSAR (ICR)MIR4770 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4770
EVEXMIR4770
GoPubMedMIR4770
iHOPMIR4770
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Nov 21 14:00:05 CET 2017

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