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MIR7641-2 (microRNA 7641-2)

Identity

Alias_symbol (synonym)hsa-mir-7641-2
Other aliasB-ATF
HGNC (Hugo) MIR7641-2
LocusID (NCBI) 102465753
Atlas_Id 70228
Location 10p15.3  [Link to chromosome band 10p15]
Location_base_pair Starts at 282037 and ends at 282086 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)MIR7641-2   50214
Cards
Entrez_Gene (NCBI)MIR7641-2  102465753  microRNA 7641-2
AliasesB-ATF; hsa-mir-7641-2
GeneCards (Weizmann)MIR7641-2
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr10:282037-282086 [Contig_View]  MIR7641-2 [Vega]
TCGA cBioPortalMIR7641-2
AceView (NCBI)MIR7641-2
Genatlas (Paris)MIR7641-2
WikiGenes102465753
SOURCE (Princeton)MIR7641-2
Genetics Home Reference (NIH)MIR7641-2
miRBaseMIR7641-2
dbDEMCMIR7641-2
Genomic and cartography
GoldenPath hg38 (UCSC)MIR7641-2  -     chr10:282037-282086 -  10p15.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR7641-2  -     10p15.3   [Description]    (hg19-Feb_2009)
EnsemblMIR7641-2 - 10p15.3 [CytoView hg19]  MIR7641-2 - 10p15.3 [CytoView hg38]
Mapping of homologs : NCBIMIR7641-2 [Mapview hg19]  MIR7641-2 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR7641-2
Gene ExpressionMIR7641-2 [ NCBI-GEO ]   MIR7641-2 [ EBI - ARRAY_EXPRESS ]   MIR7641-2 [ SEEK ]   MIR7641-2 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR7641-2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)102465753
GTEX Portal (Tissue expression)MIR7641-2
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR7641-2
DMDM Disease mutations102465753
Blocks (Seattle)MIR7641-2
Protein Interaction databases
BioGRIDMIR7641-2
STRING (EMBL)MIR7641-2
ZODIACMIR7641-2
Ontologies - Pathways
Huge Navigator MIR7641-2 [HugePedia]
snp3D : Map Gene to Disease102465753
BioCentury BCIQMIR7641-2
ClinGenMIR7641-2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD102465753
Clinical trialMIR7641-2
Miscellaneous
canSAR (ICR)MIR7641-2 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR7641-2
EVEXMIR7641-2
GoPubMedMIR7641-2
iHOPMIR7641-2
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 Nov 9 12:17:06 CET 2017

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