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MIR7978 (microRNA 7978)

Identity

Alias (NCBI)hsa-mir-7978
HGNC (Hugo) MIR7978
HGNC Alias symbhsa-mir-7978
LocusID (NCBI) 102465859
Atlas_Id 76944
Location 4p15.2  [Link to chromosome band 4p15]
Location_base_pair Starts at 21464700 and ends at 21464758 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)MIR7978   50113
Cards
Entrez_Gene (NCBI)MIR7978  102465859  microRNA 7978
Aliaseshsa-mir-7978
GeneCards (Weizmann)MIR7978
Ensembl hg19 (Hinxton)ENSG00000283281 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000283281 [Gene_View]  ENSG00000283281 [Sequence]  chr4:21464700-21464758 [Contig_View]  MIR7978 [Vega]
ICGC DataPortalENSG00000283281
TCGA cBioPortalMIR7978
AceView (NCBI)MIR7978
Genatlas (Paris)MIR7978
WikiGenes102465859
SOURCE (Princeton)MIR7978
Genetics Home Reference (NIH)MIR7978
miRBaseMIR7978
dbDEMCMIR7978
Genomic and cartography
GoldenPath hg38 (UCSC)MIR7978  -     chr4:21464700-21464758 -  4p15.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR7978  -     4p15.2   [Description]    (hg19-Feb_2009)
GoldenPathMIR7978 - 4p15.2 [CytoView hg19]  MIR7978 - 4p15.2 [CytoView hg38]
ImmunoBaseENSG00000283281
genome Data Viewer NCBIMIR7978 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR7978
Alternative Splicing GalleryENSG00000283281
Gene ExpressionMIR7978 [ NCBI-GEO ]   MIR7978 [ EBI - ARRAY_EXPRESS ]   MIR7978 [ SEEK ]   MIR7978 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR7978 [ Firebrowse - Broad ]
GenevisibleExpression of MIR7978 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)102465859
GTEX Portal (Tissue expression)MIR7978
Human Protein AtlasENSG00000283281-MIR7978 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR7978
DMDM Disease mutations102465859
Blocks (Seattle)MIR7978
Human Protein Atlas [tissue]ENSG00000283281-MIR7978 [tissue]
Protein Interaction databases
FunCoupENSG00000283281
BioGRIDMIR7978
STRING (EMBL)MIR7978
ZODIACMIR7978
Ontologies - Pathways
Huge Navigator MIR7978 [HugePedia]
snp3D : Map Gene to Disease102465859
BioCentury BCIQMIR7978
ClinGenMIR7978
Clinical trials, drugs, therapy
Protein Interactions : CTD102465859
Clinical trialMIR7978
Miscellaneous
canSAR (ICR)MIR7978 (select the gene name)
HarmonizomeMIR7978
DataMed IndexMIR7978
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR7978
EVEXMIR7978
GoPubMedMIR7978
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

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indexed on : Sat Aug 22 19:27:39 CEST 2020

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