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MED14OS (MED14 opposite strand)

Identity

Alias_namesMED14-AS1
MED14 antisense RNA 1 (non-protein coding)
MED14 antisense RNA 1
Other alias
HGNC (Hugo) MED14OS
LocusID (NCBI) 100873985
Atlas_Id 68872
Location Xp11.4  [Link to chromosome band Xp11]
Location_base_pair Starts at 40735396 and ends at 40738701 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)MED14OS   40162
Cards
Entrez_Gene (NCBI)MED14OS  100873985  MED14 opposite strand
AliasesMED14-AS1
GeneCards (Weizmann)MED14OS
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]   [Sequence]  chrX:40735396-40738701 [Contig_View]  MED14OS [Vega]
TCGA cBioPortalMED14OS
AceView (NCBI)MED14OS
Genatlas (Paris)MED14OS
WikiGenes100873985
SOURCE (Princeton)MED14OS
Genetics Home Reference (NIH)MED14OS
Genomic and cartography
GoldenPath hg38 (UCSC)MED14OS  -     chrX:40735396-40738701 +  Xp11.4   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MED14OS  -     Xp11.4   [Description]    (hg19-Feb_2009)
GoldenPathMED14OS - Xp11.4 [CytoView hg19]  MED14OS - Xp11.4 [CytoView hg38]
Mapping of homologs : NCBIMED14OS [Mapview hg19]  MED14OS [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC039399
RefSeq transcript (Entrez)NM_001289773
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MED14OS
Cluster EST : UnigeneHs.460579 [ NCBI ]
CGAP (NCI)Hs.460579
Gene ExpressionMED14OS [ NCBI-GEO ]   MED14OS [ EBI - ARRAY_EXPRESS ]   MED14OS [ SEEK ]   MED14OS [ MEM ]
Gene Expression Viewer (FireBrowse)MED14OS [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevestigatorExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100873985
GTEX Portal (Tissue expression)MED14OS
Protein : pattern, domain, 3D structure
UniProt/SwissProtP0DP75   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtP0DP75  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProP0DP75
Splice isoforms : SwissVarP0DP75
PhosPhoSitePlusP0DP75
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MED14OS
DMDM Disease mutations100873985
Blocks (Seattle)MED14OS
SuperfamilyP0DP75
Peptide AtlasP0DP75
Protein Interaction databases
DIP (DOE-UCLA)P0DP75
IntAct (EBI)P0DP75
BioGRIDMED14OS
STRING (EMBL)MED14OS
ZODIACMED14OS
Ontologies - Pathways
QuickGOP0DP75
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkMED14OS
Atlas of Cancer Signalling NetworkMED14OS
Wikipedia pathwaysMED14OS
Orthology - Evolution
OrthoDB100873985
Phylogenetic Trees/Animal Genes : TreeFamMED14OS
HOGENOMP0DP75
Homologs : HomoloGeneMED14OS
Homology/Alignments : Family Browser (UCSC)MED14OS
Gene fusions - Rearrangements
Fusion : QuiverMED14OS
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMED14OS [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MED14OS
dbVarMED14OS
ClinVarMED14OS
1000_GenomesMED14OS 
Exome Variant ServerMED14OS
Varsome BrowserMED14OS
Genetic variants : HAPMAP100873985
Genomic Variants (DGV)MED14OS [DGVbeta]
DECIPHERMED14OS [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisMED14OS 
Mutations
ICGC Data PortalMED14OS 
TCGA Data PortalMED14OS 
Broad Tumor PortalMED14OS
OASIS PortalMED14OS [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDMED14OS
BioMutasearch MED14OS
DgiDB (Drug Gene Interaction Database)MED14OS
DoCM (Curated mutations)MED14OS (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MED14OS (select a term)
intoGenMED14OS
Cancer3DMED14OS(select the gene name)
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETMED14OS
MedgenMED14OS
Genetic Testing Registry MED14OS
NextProtP0DP75 [Medical]
TSGene100873985
GENETestsMED14OS
Target ValidationMED14OS
Huge Navigator MED14OS [HugePedia]
snp3D : Map Gene to Disease100873985
BioCentury BCIQMED14OS
ClinGenMED14OS
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100873985
Clinical trialMED14OS
Miscellaneous
canSAR (ICR)MED14OS (select the gene name)
DataMed IndexMED14OS
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMED14OS
EVEXMED14OS
GoPubMedMED14OS
iHOPMED14OS
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Sep 3 15:51:52 CEST 2019

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