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

MIR5692C2 (microRNA 5692c-2)

Identity

Alias_symbol (synonym)hsa-mir-5692c-2
Other alias-
HGNC (Hugo) MIR5692C2
LocusID (NCBI) 100847017
Atlas_Id 69888
Location 7q21.3  [Link to chromosome band 7q21]
Location_base_pair Starts at 97964405 and ends at 97964481 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)MIR5692C2   43448
Cards
Entrez_Gene (NCBI)MIR5692C2  100847017  microRNA 5692c-2
Aliases
GeneCards (Weizmann)MIR5692C2
Ensembl hg19 (Hinxton)ENSG00000266668 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000266668 [Gene_View]  chr7:97964405-97964481 [Contig_View]  MIR5692C2 [Vega]
ICGC DataPortalENSG00000266668
TCGA cBioPortalMIR5692C2
AceView (NCBI)MIR5692C2
Genatlas (Paris)MIR5692C2
WikiGenes100847017
SOURCE (Princeton)MIR5692C2
Genetics Home Reference (NIH)MIR5692C2
miRBaseMIR5692C2
dbDEMCMIR5692C2
Genomic and cartography
GoldenPath hg38 (UCSC)MIR5692C2  -     chr7:97964405-97964481 -  7q21.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR5692C2  -     7q21.3   [Description]    (hg19-Feb_2009)
EnsemblMIR5692C2 - 7q21.3 [CytoView hg19]  MIR5692C2 - 7q21.3 [CytoView hg38]
Mapping of homologs : NCBIMIR5692C2 [Mapview hg19]  MIR5692C2 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR5692C2
Alternative Splicing GalleryENSG00000266668
Gene ExpressionMIR5692C2 [ NCBI-GEO ]   MIR5692C2 [ EBI - ARRAY_EXPRESS ]   MIR5692C2 [ SEEK ]   MIR5692C2 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR5692C2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100847017
GTEX Portal (Tissue expression)MIR5692C2
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR5692C2
DMDM Disease mutations100847017
Blocks (Seattle)MIR5692C2
Human Protein AtlasENSG00000266668
Protein Interaction databases
FunCoupENSG00000266668
BioGRIDMIR5692C2
STRING (EMBL)MIR5692C2
ZODIACMIR5692C2
Ontologies - Pathways
Huge Navigator MIR5692C2 [HugePedia]
snp3D : Map Gene to Disease100847017
BioCentury BCIQMIR5692C2
ClinGenMIR5692C2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100847017
Clinical trialMIR5692C2
Miscellaneous
canSAR (ICR)MIR5692C2 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR5692C2
EVEXMIR5692C2
GoPubMedMIR5692C2
iHOPMIR5692C2
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 : Mon Sep 18 13:29:50 CEST 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.