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MIR4767 (microRNA 4767)

Identity

Alias_symbol (synonym)hsa-mir-4767
Other aliasmir-4767
HGNC (Hugo) MIR4767
LocusID (NCBI) 100616467
Atlas_Id 69680
Location Xp22.31  [Link to chromosome band Xp22]
Location_base_pair Starts at 7065901 and ends at 7065978 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)MIR4767   41548
Cards
Entrez_Gene (NCBI)MIR4767  100616467  microRNA 4767
Aliasesmir-4767
GeneCards (Weizmann)MIR4767
Ensembl hg19 (Hinxton)ENSG00000264268 [Gene_View]  chrX:7065901-7065978 [Contig_View]  MIR4767 [Vega]
Ensembl hg38 (Hinxton)ENSG00000264268 [Gene_View]  chrX:7065901-7065978 [Contig_View]  MIR4767 [Vega]
ICGC DataPortalENSG00000264268
TCGA cBioPortalMIR4767
AceView (NCBI)MIR4767
Genatlas (Paris)MIR4767
WikiGenes100616467
SOURCE (Princeton)MIR4767
Genetics Home Reference (NIH)MIR4767
miRBaseMIR4767
dbDEMCMIR4767
Genomic and cartography
GoldenPath hg19 (UCSC)MIR4767  -     chrX:7065901-7065978 +  Xp22.31   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR4767  -     Xp22.31   [Description]    (hg38-Dec_2013)
EnsemblMIR4767 - Xp22.31 [CytoView hg19]  MIR4767 - Xp22.31 [CytoView hg38]
Mapping of homologs : NCBIMIR4767 [Mapview hg19]  MIR4767 [Mapview hg38]
Gene and transcription
Genbank (Entrez)LM611413
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000023 NC_018934 NT_167197 NW_004929438
Consensus coding sequences : CCDS (NCBI)MIR4767
Alternative Splicing GalleryENSG00000264268
Gene ExpressionMIR4767 [ NCBI-GEO ]   MIR4767 [ EBI - ARRAY_EXPRESS ]   MIR4767 [ SEEK ]   MIR4767 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4767 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616467
GTEX Portal (Tissue expression)MIR4767
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4767
DMDM Disease mutations100616467
Blocks (Seattle)MIR4767
Human Protein AtlasENSG00000264268
Protein Interaction databases
FunCoupENSG00000264268
BioGRIDMIR4767
STRING (EMBL)MIR4767
ZODIACMIR4767
Ontologies - Pathways
Huge Navigator MIR4767 [HugePedia]
snp3D : Map Gene to Disease100616467
BioCentury BCIQMIR4767
ClinGenMIR4767
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616467
Clinical trialMIR4767
Miscellaneous
canSAR (ICR)MIR4767 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4767
EVEXMIR4767
GoPubMedMIR4767
iHOPMIR4767
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 Mar 14 12:31:01 CET 2017

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