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MIR892C (microRNA 892c)

Identity

Alias_symbol (synonym)hsa-mir-892c
Other alias
HGNC (Hugo) MIR892C
LocusID (NCBI) 102466721
Atlas_Id 70302
Location Xq27.3  [Link to chromosome band Xq27]
Location_base_pair Starts at 145074268 and ends at 145074344 bp from pter ( according to hg19-Feb_2009)

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)MIR892C   50194
Cards
Entrez_Gene (NCBI)MIR892C  102466721  microRNA 892c
Aliaseshsa-mir-892c
GeneCards (Weizmann)MIR892C
Ensembl hg19 (Hinxton)ENSG00000252219 [Gene_View]  chrX:145074268-145074344 [Contig_View]  MIR892C [Vega]
Ensembl hg38 (Hinxton)ENSG00000252219 [Gene_View]  chrX:145074268-145074344 [Contig_View]  MIR892C [Vega]
ICGC DataPortalENSG00000252219
TCGA cBioPortalMIR892C
AceView (NCBI)MIR892C
Genatlas (Paris)MIR892C
WikiGenes102466721
SOURCE (Princeton)MIR892C
Genetics Home Reference (NIH)MIR892C
miRBaseMIR892C
dbDEMCMIR892C
Genomic and cartography
GoldenPath hg19 (UCSC)MIR892C  -     chrX:145074268-145074344 -  Xq27.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MIR892C  -     Xq27.3   [Description]    (hg38-Dec_2013)
EnsemblMIR892C - Xq27.3 [CytoView hg19]  MIR892C - Xq27.3 [CytoView hg38]
Mapping of homologs : NCBIMIR892C [Mapview hg19]  MIR892C [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000023 NC_018934 NT_011681 NW_004929447
Consensus coding sequences : CCDS (NCBI)MIR892C
Alternative Splicing GalleryENSG00000252219
Gene ExpressionMIR892C [ NCBI-GEO ]   MIR892C [ EBI - ARRAY_EXPRESS ]   MIR892C [ SEEK ]   MIR892C [ MEM ]
Gene Expression Viewer (FireBrowse)MIR892C [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)102466721
GTEX Portal (Tissue expression)MIR892C
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR892C
DMDM Disease mutations102466721
Blocks (Seattle)MIR892C
Human Protein AtlasENSG00000252219
Protein Interaction databases
FunCoupENSG00000252219
BioGRIDMIR892C
STRING (EMBL)MIR892C
ZODIACMIR892C
Ontologies - Pathways
Huge Navigator MIR892C [HugePedia]
snp3D : Map Gene to Disease102466721
BioCentury BCIQMIR892C
ClinGenMIR892C
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD102466721
Clinical trialMIR892C
Miscellaneous
canSAR (ICR)MIR892C (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR892C
EVEXMIR892C
GoPubMedMIR892C
iHOPMIR892C
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 12:33:12 CET 2017

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