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MIR767 (microRNA 767)

Identity

Alias_namesMIRN767
Alias_symbol (synonym)hsa-mir-767
Other aliasmir-767
HGNC (Hugo) MIR767
LocusID (NCBI) 768215
Atlas_Id 55378
Location Xq28  [Link to chromosome band Xq28]
Location_base_pair Starts at 152393421 and ends at 152393529 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)MIR767   33136
Cards
Entrez_Gene (NCBI)MIR767  768215  microRNA 767
AliasesMIRN767; hsa-mir-767; mir-767
GeneCards (Weizmann)MIR767
Ensembl hg19 (Hinxton)ENSG00000211583 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000211583 [Gene_View]  ENSG00000211583 [Sequence]  chrX:152393421-152393529 [Contig_View]  MIR767 [Vega]
ICGC DataPortalENSG00000211583
TCGA cBioPortalMIR767
AceView (NCBI)MIR767
Genatlas (Paris)MIR767
WikiGenes768215
SOURCE (Princeton)MIR767
Genetics Home Reference (NIH)MIR767
miRBaseMIR767
dbDEMCMIR767
Genomic and cartography
GoldenPath hg38 (UCSC)MIR767  -     chrX:152393421-152393529 -  Xq28   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR767  -     Xq28   [Description]    (hg19-Feb_2009)
EnsemblMIR767 - Xq28 [CytoView hg19]  MIR767 - Xq28 [CytoView hg38]
Mapping of homologs : NCBIMIR767 [Mapview hg19]  MIR767 [Mapview hg38]
Gene and transcription
Genbank (Entrez)LM609621
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR767
Alternative Splicing GalleryENSG00000211583
Gene ExpressionMIR767 [ NCBI-GEO ]   MIR767 [ EBI - ARRAY_EXPRESS ]   MIR767 [ SEEK ]   MIR767 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR767 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)768215
GTEX Portal (Tissue expression)MIR767
Human Protein AtlasENSG00000211583-MIR767 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR767
DMDM Disease mutations768215
Blocks (Seattle)MIR767
Human Protein Atlas [tissue]ENSG00000211583-MIR767 [tissue]
Protein Interaction databases
FunCoupENSG00000211583
BioGRIDMIR767
STRING (EMBL)MIR767
ZODIACMIR767
Ontologies - Pathways
Huge Navigator MIR767 [HugePedia]
snp3D : Map Gene to Disease768215
BioCentury BCIQMIR767
ClinGenMIR767
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD768215
Chemical/Pharm GKB GenePA164722976
Clinical trialMIR767
Miscellaneous
canSAR (ICR)MIR767 (select the gene name)
Probes
Litterature
PubMed7 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR767
EVEXMIR767
GoPubMedMIR767
iHOPMIR767
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Nov 6 11:22:56 CET 2018

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