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

MIR1199 (microRNA 1199)

Identity

Alias_symbol (synonym)hsa-mir-1199
Other alias
HGNC (Hugo) MIR1199
LocusID (NCBI) 102466515
Atlas_Id 69011
Location 19p13.12  [Link to chromosome band 19p13]
Location_base_pair Starts at 14073361 and ends at 14073479 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)MIR1199   50081
Cards
Entrez_Gene (NCBI)MIR1199  102466515  microRNA 1199
Aliaseshsa-mir-1199
GeneCards (Weizmann)MIR1199
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr19:14073361-14073479 [Contig_View]  MIR1199 [Vega]
TCGA cBioPortalMIR1199
AceView (NCBI)MIR1199
Genatlas (Paris)MIR1199
WikiGenes102466515
SOURCE (Princeton)MIR1199
Genetics Home Reference (NIH)MIR1199
miRBaseMIR1199
dbDEMCMIR1199
Genomic and cartography
GoldenPath hg38 (UCSC)MIR1199  -     chr19:14073361-14073479 +  19p13.12   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MIR1199  -     19p13.12   [Description]    (hg19-Feb_2009)
EnsemblMIR1199 - 19p13.12 [CytoView hg19]  MIR1199 - 19p13.12 [CytoView hg38]
Mapping of homologs : NCBIMIR1199 [Mapview hg19]  MIR1199 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MIR1199
Gene ExpressionMIR1199 [ NCBI-GEO ]   MIR1199 [ EBI - ARRAY_EXPRESS ]   MIR1199 [ SEEK ]   MIR1199 [ MEM ]
Gene Expression Viewer (FireBrowse)MIR1199 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)102466515
GTEX Portal (Tissue expression)MIR1199
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MIR1199
DMDM Disease mutations102466515
Blocks (Seattle)MIR1199
Protein Interaction databases
BioGRIDMIR1199
STRING (EMBL)MIR1199
ZODIACMIR1199
Ontologies - Pathways
Huge Navigator MIR1199 [HugePedia]
snp3D : Map Gene to Disease102466515
BioCentury BCIQMIR1199
ClinGenMIR1199
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD102466515
Clinical trialMIR1199
Miscellaneous
canSAR (ICR)MIR1199 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMIR1199
EVEXMIR1199
GoPubMedMIR1199
iHOPMIR1199
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 13:27:27 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.