Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumours   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

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 40594648 and ends at 40597953 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)MED14OS   40162
Cards
Entrez_Gene (NCBI)MED14OS  100873985  MED14 opposite strand
AliasesMED14-AS1
GeneCards (Weizmann)MED14OS
Ensembl hg19 (Hinxton) [Gene_View]  chrX:40594648-40597953 [Contig_View]  MED14OS [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chrX:40594648-40597953 [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 hg19 (UCSC)MED14OS  -     chrX:40594648-40597953 +  Xp11.4   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MED14OS  -     Xp11.4   [Description]    (hg38-Dec_2013)
EnsemblMED14OS - Xp11.4 [CytoView hg19]  MED14OS - Xp11.4 [CytoView hg38]
Mapping of homologs : NCBIMED14OS [Mapview hg19]  MED14OS [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC039399 HG512499
RefSeq transcript (Entrez)NM_001289773
RefSeq genomic (Entrez)NC_000023 NC_018934 NG_016325 NT_079573 NW_004929439
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]
BioGPS (Tissue expression)100873985
GTEX Portal (Tissue expression)MED14OS
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MED14OS
DMDM Disease mutations100873985
Blocks (Seattle)MED14OS
Protein Interaction databases
BioGRIDMED14OS
STRING (EMBL)MED14OS
ZODIACMED14OS
Ontologies - Pathways
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)
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

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Mar 14 12:27:56 CET 2017

Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.