Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

MIR5695 (microRNA 5695)

Identity

Alias (NCBI)-
HGNC (Hugo) MIR5695
HGNC Alias symbhsa-mir-5695
LocusID (NCBI) 100847016
Atlas_Id 69891
Location 19p13.13  [Link to chromosome band 19p13]
Location_base_pair Starts at 12920320 and ends at 12920404 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)MIR5695   43548
Cards
Entrez_Gene (NCBI)MIR5695    microRNA 5695
Aliases
GeneCards (Weizmann)MIR5695
Ensembl hg19 (Hinxton)ENSG00000266721 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000266721 [Gene_View]  ENSG00000266721 [Sequence]  chr19:12920320-12920404 [Contig_View]  MIR5695 [Vega]
ICGC DataPortalENSG00000266721
TCGA cBioPortalMIR5695
AceView (NCBI)MIR5695
Genatlas (Paris)MIR5695
SOURCE (Princeton)MIR5695
Genetics Home Reference (NIH)MIR5695
miRBaseMIR5695
dbDEMCMIR5695
Genomic and cartography
GoldenPath hg38 (UCSC)MIR5695  -     chr19:12920320-12920404 +  19p13.13   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR5695  -     19p13.13   [Description]    (hg19-Feb_2009)
GoldenPathMIR5695 - 19p13.13 [CytoView hg19]  MIR5695 - 19p13.13 [CytoView hg38]
ImmunoBaseENSG00000266721
genome Data Viewer NCBIMIR5695 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR5695
Alternative Splicing GalleryENSG00000266721
Gene ExpressionMIR5695 [ NCBI-GEO ]   MIR5695 [ EBI - ARRAY_EXPRESS ]   MIR5695 [ SEEK ]   MIR5695 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR5695 [ Firebrowse - Broad ]
GenevisibleExpression of MIR5695 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100847016
GTEX Portal (Tissue expression)MIR5695
Human Protein AtlasENSG00000266721-MIR5695 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR5695
Blocks (Seattle)MIR5695
Human Protein Atlas [tissue]ENSG00000266721-MIR5695 [tissue]
Protein Interaction databases
BioGRIDMIR5695
STRING (EMBL)MIR5695
ZODIACMIR5695
Ontologies - Pathways
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR5695
EVEXMIR5695
GoPubMedMIR5695
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 : Sat Dec 5 17:16:14 CET 2020

Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.