Atlas of Genetics and Cytogenetics in Oncology and Haematology


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MIR3910-1 (microRNA 3910-1)

Identity

Alias_symbol (synonym)hsa-mir-3910-1
Other aliasmir-3910-1
HGNC (Hugo) MIR3910-1
LocusID (NCBI) 100500821
Atlas_Id 69319
Location 9q22.31  [Link to chromosome band 9q22]
Location_base_pair Starts at 91636251 and ends at 91636361 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)MIR3910-1   38966
Cards
Entrez_Gene (NCBI)MIR3910-1  100500821  microRNA 3910-1
Aliasesmir-3910-1
GeneCards (Weizmann)MIR3910-1
Ensembl hg19 (Hinxton)ENSG00000266855 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000266855 [Gene_View]  chr9:91636251-91636361 [Contig_View]  MIR3910-1 [Vega]
ICGC DataPortalENSG00000266855
TCGA cBioPortalMIR3910-1
AceView (NCBI)MIR3910-1
Genatlas (Paris)MIR3910-1
WikiGenes100500821
SOURCE (Princeton)MIR3910-1
Genetics Home Reference (NIH)MIR3910-1
miRBaseMIR3910-1
dbDEMCMIR3910-1
Genomic and cartography
GoldenPath hg38 (UCSC)MIR3910-1  -     chr9:91636251-91636361 +  9q22.31   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR3910-1  -     9q22.31   [Description]    (hg19-Feb_2009)
EnsemblMIR3910-1 - 9q22.31 [CytoView hg19]  MIR3910-1 - 9q22.31 [CytoView hg38]
Mapping of homologs : NCBIMIR3910-1 [Mapview hg19]  MIR3910-1 [Mapview hg38]
Gene and transcription
Genbank (Entrez)LM611246
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR3910-1
Alternative Splicing GalleryENSG00000266855
Gene ExpressionMIR3910-1 [ NCBI-GEO ]   MIR3910-1 [ EBI - ARRAY_EXPRESS ]   MIR3910-1 [ SEEK ]   MIR3910-1 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR3910-1 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100500821
GTEX Portal (Tissue expression)MIR3910-1
Human Protein AtlasENSG00000266855-MIR3910-1 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR3910-1
DMDM Disease mutations100500821
Blocks (Seattle)MIR3910-1
Human Protein Atlas [tissue]ENSG00000266855-MIR3910-1 [tissue]
Protein Interaction databases
FunCoupENSG00000266855
BioGRIDMIR3910-1
STRING (EMBL)MIR3910-1
ZODIACMIR3910-1
Ontologies - Pathways
Huge Navigator MIR3910-1 [HugePedia]
snp3D : Map Gene to Disease100500821
BioCentury BCIQMIR3910-1
ClinGenMIR3910-1
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100500821
Clinical trialMIR3910-1
Miscellaneous
canSAR (ICR)MIR3910-1 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR3910-1
EVEXMIR3910-1
GoPubMedMIR3910-1
iHOPMIR3910-1
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Thu Nov 9 12:13:58 CET 2017

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