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MYEOV2 (myeloma overexpressed 2)

Identity

Other alias-
HGNC (Hugo) MYEOV2
LocusID (NCBI) 150678
Atlas_Id 70605
Location 2q37.3  [Link to chromosome band 2q37]
Location_base_pair Starts at 241070242 and ends at 241075747 bp from pter ( according to hg19-Feb_2009)
Fusion genes
(updated 2016)
BOK (2q37.3) / MYEOV2 (2q37.3)

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)MYEOV2   21314
Cards
Entrez_Gene (NCBI)MYEOV2  150678  myeloma overexpressed 2
Aliases
GeneCards (Weizmann)MYEOV2
Ensembl hg19 (Hinxton)ENSG00000172428 [Gene_View]  chr2:241070242-241075747 [Contig_View]  MYEOV2 [Vega]
Ensembl hg38 (Hinxton)ENSG00000172428 [Gene_View]  chr2:241070242-241075747 [Contig_View]  MYEOV2 [Vega]
ICGC DataPortalENSG00000172428
TCGA cBioPortalMYEOV2
AceView (NCBI)MYEOV2
Genatlas (Paris)MYEOV2
WikiGenes150678
SOURCE (Princeton)MYEOV2
Genetics Home Reference (NIH)MYEOV2
Genomic and cartography
GoldenPath hg19 (UCSC)MYEOV2  -     chr2:241070242-241075747 -  2q37.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)MYEOV2  -     2q37.3   [Description]    (hg38-Dec_2013)
EnsemblMYEOV2 - 2q37.3 [CytoView hg19]  MYEOV2 - 2q37.3 [CytoView hg38]
Mapping of homologs : NCBIMYEOV2 [Mapview hg19]  MYEOV2 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AF453951 AF487338 BC033955 BC140452 CN304277
RefSeq transcript (Entrez)NM_001163424 NM_138336
RefSeq genomic (Entrez)NC_000002 NC_018913 NT_005403 NW_004929308
Consensus coding sequences : CCDS (NCBI)MYEOV2
Cluster EST : UnigeneHs.293884 [ NCBI ]
CGAP (NCI)Hs.293884
Alternative Splicing GalleryENSG00000172428
Gene ExpressionMYEOV2 [ NCBI-GEO ]   MYEOV2 [ EBI - ARRAY_EXPRESS ]   MYEOV2 [ SEEK ]   MYEOV2 [ MEM ]
Gene Expression Viewer (FireBrowse)MYEOV2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)150678
GTEX Portal (Tissue expression)MYEOV2
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ8WXC6   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ8WXC6  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ8WXC6
Splice isoforms : SwissVarQ8WXC6
PhosPhoSitePlusQ8WXC6
Domains : Interpro (EBI)MYEOV2   
Domain families : Pfam (Sanger)MYEOV2 (PF15004)   
Domain families : Pfam (NCBI)pfam15004   
Conserved Domain (NCBI)MYEOV2
DMDM Disease mutations150678
Blocks (Seattle)MYEOV2
SuperfamilyQ8WXC6
Human Protein AtlasENSG00000172428
Peptide AtlasQ8WXC6
HPRD17306
IPIIPI00103507   IPI00890829   
Protein Interaction databases
DIP (DOE-UCLA)Q8WXC6
IntAct (EBI)Q8WXC6
FunCoupENSG00000172428
BioGRIDMYEOV2
STRING (EMBL)MYEOV2
ZODIACMYEOV2
Ontologies - Pathways
QuickGOQ8WXC6
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkMYEOV2
Atlas of Cancer Signalling NetworkMYEOV2
Wikipedia pathwaysMYEOV2
Orthology - Evolution
OrthoDB150678
GeneTree (enSembl)ENSG00000172428
Phylogenetic Trees/Animal Genes : TreeFamMYEOV2
HOVERGENQ8WXC6
HOGENOMQ8WXC6
Homologs : HomoloGeneMYEOV2
Homology/Alignments : Family Browser (UCSC)MYEOV2
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerMYEOV2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)MYEOV2
dbVarMYEOV2
ClinVarMYEOV2
1000_GenomesMYEOV2 
Exome Variant ServerMYEOV2
ExAC (Exome Aggregation Consortium)MYEOV2 (select the gene name)
Genetic variants : HAPMAP150678
Genomic Variants (DGV)MYEOV2 [DGVbeta]
DECIPHER (Syndromes)2:241070242-241075747  ENSG00000172428
CONAN: Copy Number AnalysisMYEOV2 
Mutations
ICGC Data PortalMYEOV2 
TCGA Data PortalMYEOV2 
Broad Tumor PortalMYEOV2
OASIS PortalMYEOV2 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICMYEOV2  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDMYEOV2
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD - Leiden Open Variation Database
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch MYEOV2
DgiDB (Drug Gene Interaction Database)MYEOV2
DoCM (Curated mutations)MYEOV2 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)MYEOV2 (select a term)
intoGenMYEOV2
Cancer3DMYEOV2(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenMYEOV2
Genetic Testing Registry MYEOV2
NextProtQ8WXC6 [Medical]
TSGene150678
GENETestsMYEOV2
Huge Navigator MYEOV2 [HugePedia]
snp3D : Map Gene to Disease150678
BioCentury BCIQMYEOV2
ClinGenMYEOV2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD150678
Chemical/Pharm GKB GenePA142671302
Clinical trialMYEOV2
Miscellaneous
canSAR (ICR)MYEOV2 (select the gene name)
Probes
Litterature
PubMed6 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMYEOV2
EVEXMYEOV2
GoPubMedMYEOV2
iHOPMYEOV2
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 12:34:15 CET 2017

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