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

MIR4795 (microRNA 4795)

Identity

Alias_symbol (synonym)hsa-mir-4795
Other alias-
HGNC (Hugo) MIR4795
LocusID (NCBI) 100616161
Atlas_Id 69709
Location 3p11.2  [Link to chromosome band 3p11]
Location_base_pair Starts at 87226189 and ends at 87226277 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)MIR4795   41757
Cards
Entrez_Gene (NCBI)MIR4795  100616161  microRNA 4795
Aliases
GeneCards (Weizmann)MIR4795
Ensembl hg19 (Hinxton)ENSG00000264119 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000264119 [Gene_View]  chr3:87226189-87226277 [Contig_View]  MIR4795 [Vega]
ICGC DataPortalENSG00000264119
TCGA cBioPortalMIR4795
AceView (NCBI)MIR4795
Genatlas (Paris)MIR4795
WikiGenes100616161
SOURCE (Princeton)MIR4795
Genetics Home Reference (NIH)MIR4795
miRBaseMIR4795
dbDEMCMIR4795
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4795  -     chr3:87226189-87226277 -  3p11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4795  -     3p11.2   [Description]    (hg19-Feb_2009)
EnsemblMIR4795 - 3p11.2 [CytoView hg19]  MIR4795 - 3p11.2 [CytoView hg38]
Mapping of homologs : NCBIMIR4795 [Mapview hg19]  MIR4795 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4795
Alternative Splicing GalleryENSG00000264119
Gene ExpressionMIR4795 [ NCBI-GEO ]   MIR4795 [ EBI - ARRAY_EXPRESS ]   MIR4795 [ SEEK ]   MIR4795 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4795 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100616161
GTEX Portal (Tissue expression)MIR4795
Human Protein AtlasENSG00000264119-MIR4795 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4795
DMDM Disease mutations100616161
Blocks (Seattle)MIR4795
Human Protein Atlas [tissue]ENSG00000264119-MIR4795 [tissue]
Protein Interaction databases
FunCoupENSG00000264119
BioGRIDMIR4795
STRING (EMBL)MIR4795
ZODIACMIR4795
Ontologies - Pathways
Huge Navigator MIR4795 [HugePedia]
snp3D : Map Gene to Disease100616161
BioCentury BCIQMIR4795
ClinGenMIR4795
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100616161
Clinical trialMIR4795
Miscellaneous
canSAR (ICR)MIR4795 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGee Re&ergnces Into Functions (Entrez)
CoreMineMIR4795
EVEXMIR4795
GoPubMedMIR4795
iHOPMIR4795
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 13:08:23 CET 2017

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.