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MYEOV myeloma overexpressed (in a subset of t(11;14) positive multiple myelomas)

Identity

Other namesOCIM
HGNC (Hugo) MYEOV
Location 11q13
Location_base_pair Starts at 69061622 and ends at 69064753 bp from pter ( according to hg19-Feb_2009)  [Mapping]
Local_order 350 kb centromeric of cyclin D1
Note detected by application of the NIH/3T3 tumorigenicity assay. However MYEOV cDNA was not positive in NIH/3T3 assay.

DNA/RNA

Description 2 exons; 3.5 kb transcript represents unspliced mRNA.
Transcription main transcript 2.8 kb (broad band because of alternative splice products); minor transcript 3.5 kb.; coding sequence 313 or 255 amino acids. In normal tissues hardly any expression detectable. High expression in a subset of multiple myeloma cell lines with a t(11;14)(q13;q32) and in breast tumors and esophageal squamous cell carcinomas with or without 11q13 amplification.

Protein

Description 313 or 255 amino acids; contains one RNP-1 motif and 6 regions that might function as a transmembrane domain. Leucine-rich stretch at C-terminal.
Expression 5Ô UTR inhibits efficient translation of the protein
Localisation in endoplasmic reticulum and mitochondria.

Implicated in

Entity t(11;14)(q13;q32)
Disease subset of multiple myeloma cell lines with t(11;14)(q13;q32)
Cytogenetics myeov overexpression due to juxtaposition to the 5' enhancer or the most telomeric 3' enhancer of the immunoglobulin heavy chain (IgH).
  
Entity 11q13 amplification and/or overexpression
Disease breast cancer; esophageal squamous cell carcinomas.
Prognosis MYEOV DNA amplification correlated with estrogen and progesterone receptor-positive cancer, invasive lobular carcinoma type and axillary nodal involvement. In contrast to Cyclin D1 amplification, no association with disease outcome could be found.
  

External links

Nomenclature
HGNC (Hugo)MYEOV   7563
Entrez_Gene (NCBI)MYEOV  26579  myeloma overexpressed (in a subset of t(11;14) positive multiple myelomas)
Cards
AtlasMYEOVID395
GeneCards (Weizmann)MYEOV
Ensembl (Hinxton)ENSG00000172927 [Gene_View]  MYEOV [Vega]
AceView (NCBI)MYEOV
Genatlas (Paris)MYEOV
euGene (Indiana)26579
SOURCE (Stanford)NM_138768
Gene Expression (Array Express) ENSG00000172927
Genomic and cartography
GoldenPath (UCSC)MYEOV  -  11q13   chr11:69061622-69064753 +  11q13   [Description]    (hg19-Feb_2009)
EnsemblMYEOV - 11q13 [CytoView]
Mapping of homologs : NCBIMYEOV [Mapview]
OMIM605625   
Gene and transcription
Gene : Genbank (Entrez)AJ223366 AJ223366 AK026148 AK290121 BC011815
Reference sequence (RefSeq transcript) :SRSNM_138768
Reference transcript : EntrezNM_138768
RefSeq genomic : SRSAC_000054 AC_000143 NC_000011 NT_167190 NW_001838026 NW_925106
RefSeq genomic : EntrezAC_000054 AC_000143 NC_000011 NT_167190 NW_001838026 NW_925106
Consensus coding sequences : CCDS NCBIMYEOV
Cluster EST : UnigeneHs.523848 [ SRS ] Hs.523848 [ NCBI ]
Alternative Splicing : Fast-db (Paris)11061
Protein : pattern, domain, 3D structure
Protein : UniProt/SwissProtQ96EZ4 (SRS) Q96EZ4 (Expasy) Q96EZ4 (Uniprot)
With graphics : InterProQ96EZ4
Splice isoforms : VarSplice FASTAQ96EZ4(VarSplice FASTA)
Related proteins : CluSTrQ96EZ4
Domain families : Pfam SRS
Domain families : Pfam Sanger
Domain families : Pfam NCBI
Blocks (Seattle)Q96EZ4
Crystal structure of protein : PDB SRS
Crystal structure of protein : PDBSum
Crystal structure of protein : IMB
Crystal structure of protein : PDB RSDB
Human Protein AtlasENSG00000172927
HPRD16130
Protein Interaction databases
DIP (DOE-UCLA)Q96EZ4
IntAct (EBI)Q96EZ4
FunCoupENSG00000172927
Polymorphism : SNP, mutations, diseases
Single Nucleotide Polymorphism (SNP) : dbSNP NCBIMYEOV
SNP : GeneSNP UtahMYEOV
SNP : HGBaseMYEOV
Genetic variants : HAPMAPMYEOV
Somatic Mutations in Cancer : COSMICMYEOV 
Mutations and Diseases : HGMDMYEOV
Hereditary diseases : OMIM605625   
Hereditary diseases : GENETests605625   
Diseases : Genetic AssociationMYEOV
General knowledge
Homologs : HomoloGeneMYEOV
Homology/Alignments : Family Browser UCSCMYEOV
Phylogenetic Trees/Animal Genes : TreeFamMYEOV
Chemical/Protein Interactions : CTD26579
Keywords Ontology : AmiGO
Keywords Ontology : EGO-EBI
Pathways : BIOCARTA
Pathways : KEGG
Other databases
Probes
Probes : ImagenesMYEOV Related clones (RZPD - Berlin)
Literature
PubMed12 Pubmed reference(s) in Entrez
PubGeneMYEOV

Bibliography

Concurrent activation of a novel putative transforming gene, myeov, and cyclin D1 in a subset of multiple myeloma cell lines with t(11;14)(q13;q32).
Janssen JW, Vaandrager JW, Heuser T, Jauch A, Kluin PM, Geelen E, Bergsagel PL, Kuehl WM, Drexler HG, Otsuki T, Bartram CR, Schuuring E
Blood. 2000 ; 95 (8) : 2691-2698.
PMID 10753852
 
MYEOV, a gene at 11q13, is coamplified with CCND1, but epigenetically inactivated in a subset of esophageal squamous cell carcinomas.
Janssen JW, Imoto I, Inoue J, Shimada Y, Ueda M, Imamura M, Bartram CR, Inazawa J
Journal of human genetics. 2002 ; 47 (9) : 460-464.
PMID 12202983
 
MYEOV: a candidate gene for DNA amplification events occurring centromeric to CCND1 in breast cancer.
Janssen JW, Cuny M, Orsetti B, Rodriguez C, Vallˆ©s H, Bartram CR, Schuuring E, Theillet C
International journal of cancer. Journal international du cancer. 2002 ; 102 (6) : 608-614.
PMID 12448002
 
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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Contributor(s)

Written12-2002Johannes W.G. Janssen
Janssen Institut für Humangenetik Universitätsklinikum Heidelberg Im Neuenheimer Feld 328 D-69120 Heidelberg, Germany

Citation

This paper should be referenced as such :
Janssen JWG . MYEOV myeloma overexpressed (in a subset of t(11;14) positive multiple myelomas). Atlas Genet Cytogenet Oncol Haematol. December 2002 .
URL : http://AtlasGeneticsOncology.org/Genes/MYEOVID395.html

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Thu Jul 15 14:43:27 CEST 2010

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