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Q96EZ4 (MYEOV_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified January 25, 2012. Version 68. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (4) | Third-party data text xml rdf/xml gff fasta
to top of pageNames·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Web links·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
Myeloma-overexpressed gene protein
Alternative name(s):
Oncogene in multiple myeloma
Gene names
Name:MYEOV
Synonyms:OCIM
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length313 AA.
Sequence statusComplete.
Protein existenceEvidence at transcript level

General annotation (Comments)

Developmental stage

Overexpressed in tumor cells lines with a t(11;14)(q13;q32) translocation.

Sequence caution

The sequence CAB65726.1 differs from that shown. Reason: Erroneous initiation. Translation N-terminally extended.

Ontologies

Keywords
   Coding sequence diversityPolymorphism
   DiseaseProto-oncogene
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
None. [Check GOA]

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 313313Myeloma-overexpressed gene protein
PRO_0000096668

Natural variations

Natural variant1591V → A. Ref.1 Ref.3
Corresponds to variant rs7103126 [ dbSNP | Ensembl ].
VAR_016603
Natural variant1981R → Q. Ref.1
Corresponds to variant rs11539762 [ dbSNP | Ensembl ].
VAR_056948
Natural variant2711G → R. Ref.1
Corresponds to variant rs11228610 [ dbSNP | Ensembl ].
VAR_056949
Natural variant2841P → T.
Corresponds to variant rs12274095 [ dbSNP | Ensembl ].
VAR_056950

Experimental info

Sequence conflict2191M → V in AAH11815. Ref.3

Sequences

Sequence LengthMass (Da)Tools
Q96EZ4 [UniParc].

Last modified May 18, 2010. Version 2.
Checksum: 292ABC0D6AFA52B0

FASTA31333,556
        10         20         30         40         50         60 
MALRICVTYT PALPIGLCTR CCLCLEQSPS WCHCLRGVSF LTFHLHQSVP LGDRDSLLMF 

        70         80         90        100        110        120 
TRQAGHFVEG SKAGRSRGRL CLSQALRVAV RGAFVSLWFA AGAGDRERNK GDKGAQTGAG 

       130        140        150        160        170        180 
LSQEAEDVDV SRARRVTDAP QGTLCGTGNR NSGSQSARVV GVAHLGEAFR VGVEQAISSC 

       190        200        210        220        230        240 
PEEVHGRHGL SMEIMWARMD VALRSPGRGL LAGAGALCMT LAESSCPDYE RGRRACLTLH 

       250        260        270        280        290        300 
RHPTPHCSTW GLPLRVAGSW LTVVTVEALG GWRMGVRRTG QVGPTMHPPP VSGASPLLLH 

       310 
HLLLLLLIII LTC 

« Hide

References

« Hide 'large scale' references
[1]"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 J.W.G., Vaandrager J.W., Heuser T., Jauch A., Kluin P.M., Geelen E., Bergsagel P.L., Kuehl W.M., Drexler H.G., Otsuki T., Bartram C.R., Schuuring E.
Blood 95:2691-2698(2000) [PubMed: 10753852] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA], VARIANTS ALA-159; GLN-198 AND ARG-271.
Tissue: Stomach cancer.
[2]"Human chromosome 11 DNA sequence and analysis including novel gene identification."
Taylor T.D., Noguchi H., Totoki Y., Toyoda A., Kuroki Y., Dewar K., Lloyd C., Itoh T., Takeda T., Kim D.-W., She X., Barlow K.F., Bloom T., Bruford E., Chang J.L., Cuomo C.A., Eichler E., FitzGerald M.G. expand/collapse author list , Jaffe D.B., LaButti K., Nicol R., Park H.-S., Seaman C., Sougnez C., Yang X., Zimmer A.R., Zody M.C., Birren B.W., Nusbaum C., Fujiyama A., Hattori M., Rogers J., Lander E.S., Sakaki Y.
Nature 440:497-500(2006) [PubMed: 16554811] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[3]"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
The MGC Project Team
Genome Res. 14:2121-2127(2004) [PubMed: 15489334] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA], VARIANT ALA-159.
Tissue: Brain.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AJ223366 mRNA. Translation: CAB65727.1.
AJ223366 mRNA. Translation: CAB65726.1. Different initiation.
AP005379 Genomic DNA. No translation available.
BC011815 mRNA. Translation: AAH11815.1.
IPIIPI00305042.
RefSeqNP_620123.2. NM_138768.2.
UniGeneHs.523848.

3D structure databases

ProteinModelPortalQ96EZ4.
ModBaseSearch...

Protein-protein interaction databases

STRINGQ96EZ4.

Polymorphism databases

DMDM296439231.

Proteomic databases

PRIDEQ96EZ4.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000308946; ENSP00000308330; ENSG00000172927.
GeneID26579.
KEGGhsa:26579.

Organism-specific databases

CTD26579.
GeneCardsGC11P069061.
H-InvDBHIX0009887.
HGNCHGNC:7563. MYEOV.
HPAHPA012949.
MIM605625. gene.
neXtProtNX_Q96EZ4.
PharmGKBPA31362.
GenAtlasSearch...

Phylogenomic databases

eggNOGprNOG21479.
GeneTreeENSGT00400000022774.
HOVERGENHBG052548.
OMASCPEEVH.
OrthoDBEOG4RXZ0T.
PhylomeDBQ96EZ4.

Gene expression databases

ArrayExpressQ96EZ4.
BgeeQ96EZ4.
CleanExHS_MYEOV.
GenevestigatorQ96EZ4.
GermOnlineENSG00000172927. Homo sapiens.

Family and domain databases

ProtoNetSearch...

Other

NextBio48930.
SOURCESearch...

Entry information

Entry nameMYEOV_HUMAN
AccessionPrimary (citable) accession number: Q96EZ4
Secondary accession number(s): Q9UGN6, Q9UGN7
Entry history
Integrated into UniProtKB/Swiss-Prot: August 22, 2003
Last sequence update: May 18, 2010
Last modified: January 25, 2012
This is version 68 of the entry and version 2 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation programChordata Protein Annotation Program
DisclaimerAny medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care.

Relevant documents

Human chromosome 11

Human chromosome 11: entries, gene names and cross-references to MIM

Human entries with polymorphisms or disease mutations

List of human entries with polymorphisms or disease mutations

Human polymorphisms and disease mutations

Index of human polymorphisms and disease mutations

MIM cross-references

Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot