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MEG9 (maternally expressed 9 (non-protein coding))

Identity

Alias_symbol (synonym)LINC00584
Other alias
HGNC (Hugo) MEG9
LocusID (NCBI) 100507257
Atlas_Id 68893
Location 14q32.31  [Link to chromosome band 14q32]
Location_base_pair Starts at 101536248 and ends at 101539273 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)MEG9   43874
Cards
Entrez_Gene (NCBI)MEG9  100507257  maternally expressed 9 (non-protein coding)
AliasesLINC00584
GeneCards (Weizmann)MEG9
Ensembl hg19 (Hinxton)ENSG00000223403 [Gene_View]  chr14:101536248-101539273 [Contig_View]  MEG9 [Vega]
Ensembl hg38 (Hinxton)ENSG00000223403 [Gene_View]  chr14:101536248-101539273 [Contig_View]  MEG9 [Vega]
ICGC DataPortalENSG00000223403
TCGA cBioPortalMEG9
AceView (NCBI)MEG9
Genatlas (Paris)MEG9
WikiGenes100507257
SOURCE (Princeton)MEG9
Genetics Home Reference (NIH)MEG9
Genomic and cartography
GoldenPath hg19 (UCSC)MEG9  -     chr14:101536248-101539273 +  14q32.31   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MEG9  -     14q32.31   [Description]    (hg38-Dec_2013)
EnsemblMEG9 - 14q32.31 [CytoView hg19]  MEG9 - 14q32.31 [CytoView hg38]
Mapping of homologs : NCBIMEG9 [Mapview hg19]  MEG9 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK021527 AK094562 CK824083 HG506630 HG506631
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000014 NC_018925 NT_026437 NW_004929393
Consensus coding sequences : CCDS (NCBI)MEG9
Cluster EST : UnigeneHs.301755 [ NCBI ]
CGAP (NCI)Hs.301755
Alternative Splicing GalleryENSG00000223403
Gene ExpressionMEG9 [ NCBI-GEO ]   MEG9 [ EBI - ARRAY_EXPRESS ]   MEG9 [ SEEK ]   MEG9 [ MEM ]
Gene Expression Viewer (FireBrowse)MEG9 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100507257
GTEX Portal (Tissue expression)MEG9
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MEG9
DMDM Disease mutations100507257
Blocks (Seattle)MEG9
Human Protein AtlasENSG00000223403
Protein Interaction databases
FunCoupENSG00000223403
BioGRIDMEG9
STRING (EMBL)MEG9
ZODIACMEG9
Ontologies - Pathways
Huge Navigator MEG9 [HugePedia]
snp3D : Map Gene to Disease100507257
BioCentury BCIQMEG9
ClinGenMEG9
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100507257
Clinical trialMEG9
Miscellaneous
canSAR (ICR)MEG9 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMEG9
EVEXMEG9
GoPubMedMEG9
iHOPMEG9
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 12:28:00 CET 2017

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