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

MIR4712 (microRNA 4712)

Identity

Alias (NCBI)-
HGNC (Hugo) MIR4712
HGNC Alias symbhsa-mir-4712
LocusID (NCBI) 100616396
Atlas_Id 69626
Location 15q21.2  [Link to chromosome band 15q21]
Location_base_pair Starts at 50360329 and ends at 50360410 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)MIR4712   41732
Cards
Entrez_Gene (NCBI)MIR4712  100616396  microRNA 4712
Aliases
GeneCards (Weizmann)MIR4712
Ensembl hg19 (Hinxton)ENSG00000284284 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000284284 [Gene_View]  ENSG00000284284 [Sequence]  chr15:50360329-50360410 [Contig_View]  MIR4712 [Vega]
ICGC DataPortalENSG00000284284
TCGA cBioPortalMIR4712
AceView (NCBI)MIR4712
Genatlas (Paris)MIR4712
WikiGenes100616396
SOURCE (Princeton)MIR4712
Genetics Home Reference (NIH)MIR4712
miRBaseMIR4712
dbDEMCMIR4712
Genomic and cartography
GoldenPath hg38 (UCSC)MIR4712  -     chr15:50360329-50360410 +  15q21.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR4712  -     15q21.2   [Description]    (hg19-Feb_2009)
GoldenPathMIR4712 - 15q21.2 [CytoView hg19]  MIR4712 - 15q21.2 [CytoView hg38]
ImmunoBaseENSG00000284284
genome Data Viewer NCBIMIR4712 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR4712
Alternative Splicing GalleryENSG00000284284
Gene ExpressionMIR4712 [ NCBI-GEO ]   MIR4712 [ EBI - ARRAY_EXPRESS ]   MIR4712 [ SEEK ]   MIR4712 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR4712 [ Firebrowse - Broad ]
GenevisibleExpression of MIR4712 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100616396
GTEX Portal (Tissue expression)MIR4712
Human Protein AtlasENSG00000284284-MIR4712 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR4712
DMDM Disease mutations100616396
Blocks (Seattle)MIR4712
Human Protein Atlas [tissue]ENSG00000284284-MIR4712 [tissue]
Protein Interaction databases
FunCoupENSG00000284284
BioGRIDMIR4712
STRING (EMBL)MIR4712
ZODIACMIR4712
Ontologies - Pathways
Huge Navigator MIR4712 [HugePedia]
snp3D : Map Gene to Disease100616396
BioCentury BCIQMIR4712
ClinGenMIR4712
Clinical trials, drugs, therapy
Protein Interactions : CTD100616396
Clinical trialMIR4712
Miscellaneous
canSAR (ICR)MIR4712 (select the gene name)
HarmonizomeMIR4712
DataMed IndexMIR4712
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR4712
EVEXMIR4712
GoPubMedMIR4712
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 : Thu Jul 16 16:15:56 CEST 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.