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MIRLET7F2 (microRNA let-7f-2)

Identity

Alias_namesMIRNLET7F2
Alias_symbol (synonym)hsa-let-7f-2
Other aliasLET7F2
let-7f-2
HGNC (Hugo) MIRLET7F2
LocusID (NCBI) 406889
Atlas_Id 54876
Location Xp11.22  [Link to chromosome band Xp11]
Location_base_pair Starts at 53557192 and ends at 53557274 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)MIRLET7F2   31484
Cards
Entrez_Gene (NCBI)MIRLET7F2  406889  microRNA let-7f-2
AliasesLET7F2; MIRNLET7F2; let-7f-2
GeneCards (Weizmann)MIRLET7F2
Ensembl hg19 (Hinxton)ENSG00000208012 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000208012 [Gene_View]  ENSG00000208012 [Sequence]  chrX:53557192-53557274 [Contig_View]  MIRLET7F2 [Vega]
ICGC DataPortalENSG00000208012
TCGA cBioPortalMIRLET7F2
AceView (NCBI)MIRLET7F2
Genatlas (Paris)MIRLET7F2
WikiGenes406889
SOURCE (Princeton)MIRLET7F2
Genetics Home Reference (NIH)MIRLET7F2
miRBaseMIRLET7F2
dbDEMCMIRLET7F2
Genomic and cartography
GoldenPath hg38 (UCSC)MIRLET7F2  -     chrX:53557192-53557274 -  Xp11.22   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIRLET7F2  -     Xp11.22   [Description]    (hg19-Feb_2009)
EnsemblMIRLET7F2 - Xp11.22 [CytoView hg19]  MIRLET7F2 - Xp11.22 [CytoView hg38]
Mapping of homologs : NCBIMIRLET7F2 [Mapview hg19]  MIRLET7F2 [Mapview hg38]
OMIM300721   
Gene and transcription
Genbank (Entrez)AJ421732 LM608157
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIRLET7F2
Alternative Splicing GalleryENSG00000208012
Gene ExpressionMIRLET7F2 [ NCBI-GEO ]   MIRLET7F2 [ EBI - ARRAY_EXPRESS ]   MIRLET7F2 [ SEEK ]   MIRLET7F2 [ MEM ]
Gene Expression Viewer (FireBrowse)MIRLET7F2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)406889
GTEX Portal (Tissue expression)MIRLET7F2
Human Protein AtlasENSG00000208012-MIRLET7F2 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIRLET7F2
DMDM Disease mutations406889
Blocks (Seattle)MIRLET7F2
Human Protein Atlas [tissue]ENSG00000208012-MIRLET7F2 [tissue]
Protein Interaction databases
FunCoupENSG00000208012
BioGRIDMIRLET7F2
STRING (EMBL)MIRLET7F2
ZODIACMIRLET7F2
Ontologies - Pathways
Huge Navigator MIRLET7F2 [HugePedia]
snp3D : Map Gene to Disease406889
BioCentury BCIQMIRLET7F2
ClinGenMIRLET7F2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD406889
Chemical/Pharm GKB GenePA164723035
Clinical trialMIRLET7F2
Miscellaneous
canSAR (ICR)MIRLET7F2 (select the gene name)
Probes
Litterature
PubMed16 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIRLET7F2
EVEXMIRLET7F2
GoPubMedMIRLET7F2
iHOPMIRLET7F2
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Fri Jun 22 16:38:08 CEST 2018

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