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

MIR1292 (microRNA 1292)

Identity

Alias_namesMIRN1292
Alias_symbol (synonym)hsa-mir-1292
Other aliasmir-1292
HGNC (Hugo) MIR1292
LocusID (NCBI) 100302138
Atlas_Id 69062
Location 20p13  [Link to chromosome band 20p13]
Location_base_pair Starts at 2652777 and ends at 2652842 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)MIR1292   35364
Cards
Entrez_Gene (NCBI)MIR1292  100302138  microRNA 1292
AliasesMIRN1292; hsa-mir-1292; mir-1292
GeneCards (Weizmann)MIR1292
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr20:2652777-2652842 [Contig_View]  MIR1292 [Vega]
TCGA cBioPortalMIR1292
AceView (NCBI)MIR1292
Genatlas (Paris)MIR1292
WikiGenes100302138
SOURCE (Princeton)MIR1292
Genetics Home Reference (NIH)MIR1292
miRBaseMIR1292
dbDEMCMIR1292
Genomic and cartography
GoldenPath hg38 (UCSC)MIR1292  -     chr20:2652777-2652842 +  20p13   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR1292  -     20p13   [Description]    (hg19-Feb_2009)
EnsemblMIR1292 - 20p13 [CytoView hg19]  MIR1292 - 20p13 [CytoView hg38]
Mapping of homologs : NCBIMIR1292 [Mapview hg19]  MIR1292 [Mapview hg38]
OMIM614155   
Gene and transcription
Genbank (Entrez)LM610176
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR1292
Gene ExpressionMIR1292 [ NCBI-GEO ]   MIR1292 [ EBI - ARRAY_EXPRESS ]   MIR1292 [ SEEK ]   MIR1292 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR1292 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100302138
GTEX Portal (Tissue expression)MIR1292
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR1292
DMDM Disease mutations100302138
Blocks (Seattle)MIR1292
Protein Interaction databases
BioGRIDMIR1292
STRING (EMBL)MIR1292
ZODIACMIR1292
Ontologies - Pathways
Huge Navigator MIR1292 [HugePedia]
snp3D : Map Gene to Disease100302138
BioCentury BCIQMIR1292
ClinGenMIR1292
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100302138
Chemical/Pharm GKB GenePA164722446
Clinical trialMIR1292
Miscellaneous
canSAR (ICR)MIR1292 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR1292
EVEXMIR1292
GoPubMedMIR1292
iHOPMIR1292
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 12:13:04 CET 2017

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.