Atlas of Genetics and Cytogenetics in Oncology and Haematology


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MIR5692C1 (microRNA 5692c-1)

Identity

Alias_symbol (synonym)hsa-mir-5692c-1
Other alias-
HGNC (Hugo) MIR5692C1
LocusID (NCBI) 100847082
Atlas_Id 69887
Location 5q31.1  [Link to chromosome band 5q31]
Location_base_pair Starts at 135802985 and ends at 135803075 bp from pter ( according to hg38-Dec_2013)

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)MIR5692C1   43506
Cards
Entrez_Gene (NCBI)MIR5692C1  100847082  microRNA 5692c-1
Aliases
GeneCards (Weizmann)MIR5692C1
Ensembl hg19 (Hinxton)ENSG00000265924 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000265924 [Gene_View]  chr5:135802985-135803075 [Contig_View]  MIR5692C1 [Vega]
ICGC DataPortalENSG00000265924
TCGA cBioPortalMIR5692C1
AceView (NCBI)MIR5692C1
Genatlas (Paris)MIR5692C1
WikiGenes100847082
SOURCE (Princeton)MIR5692C1
Genetics Home Reference (NIH)MIR5692C1
miRBaseMIR5692C1
dbDEMCMIR5692C1
Genomic and cartography
GoldenPath hg38 (UCSC)MIR5692C1  -     chr5:135802985-135803075 -  5q31.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR5692C1  -     5q31.1   [Description]    (hg19-Feb_2009)
EnsemblMIR5692C1 - 5q31.1 [CytoView hg19]  MIR5692C1 - 5q31.1 [CytoView hg38]
Mapping of homologs : NCBIMIR5692C1 [Mapview hg19]  MIR5692C1 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR5692C1
Alternative Splicing GalleryENSG00000265924
Gene ExpressionMIR5692C1 [ NCBI-GEO ]   MIR5692C1 [ EBI - ARRAY_EXPRESS ]   MIR5692C1 [ SEEK ]   MIR5692C1 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR5692C1 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100847082
GTEX Portal (Tissue expression)MIR5692C1
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR5692C1
DMDM Disease mutations100847082
Blocks (Seattle)MIR5692C1
Human Protein AtlasENSG00000265924
Protein Interaction databases
FunCoupENSG00000265924
BioGRIDMIR5692C1
STRING (EMBL)MIR5692C1
ZODIACMIR5692C1
Ontologies - Pathways
Huge Navigator MIR5692C1 [HugePedia]
snp3D : Map Gene to Disease100847082
BioCentury BCIQMIR5692C1
ClinGenMIR5692C1
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100847082
Clinical trialMIR5692C1
Miscellaneous
canSAR (ICR)MIR5692C1 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR5692C1
EVEXMIR5692C1
GoPubMedMIR5692C1
iHOPMIR5692C1
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 : Fri May 19 11:41:49 CEST 2017

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