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CCNB2 (cyclin B2)

Identity

Alias_symbol (synonym)HsT17299
Other alias
HGNC (Hugo) CCNB2
LocusID (NCBI) 9133
Atlas_Id 953
Location 15q22.2  [Link to chromosome band 15q22]
Location_base_pair Starts at 59397284 and ends at 59417244 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)CCNB2   1580
Cards
Entrez_Gene (NCBI)CCNB2  9133  cyclin B2
AliasesHsT17299
GeneCards (Weizmann)CCNB2
Ensembl hg19 (Hinxton)ENSG00000157456 [Gene_View]  chr15:59397284-59417244 [Contig_View]  CCNB2 [Vega]
Ensembl hg38 (Hinxton)ENSG00000157456 [Gene_View]  chr15:59397284-59417244 [Contig_View]  CCNB2 [Vega]
ICGC DataPortalENSG00000157456
TCGA cBioPortalCCNB2
AceView (NCBI)CCNB2
Genatlas (Paris)CCNB2
WikiGenes9133
SOURCE (Princeton)CCNB2
Genetics Home Reference (NIH)CCNB2
Genomic and cartography
GoldenPath hg19 (UCSC)CCNB2  -     chr15:59397284-59417244 +  15q22.2   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)CCNB2  -     15q22.2   [Description]    (hg38-Dec_2013)
EnsemblCCNB2 - 15q22.2 [CytoView hg19]  CCNB2 - 15q22.2 [CytoView hg38]
Mapping of homologs : NCBICCNB2 [Mapview hg19]  CCNB2 [Mapview hg38]
OMIM602755   
Gene and transcription
Genbank (Entrez)AB020981 AF002822 AF087910 AK001404 AK222611
RefSeq transcript (Entrez)NM_004701
RefSeq genomic (Entrez)NC_000015 NC_018926 NT_010194 NW_004929398
Consensus coding sequences : CCDS (NCBI)CCNB2
Cluster EST : UnigeneHs.194698 [ NCBI ]
CGAP (NCI)Hs.194698
Alternative Splicing GalleryENSG00000157456
Gene ExpressionCCNB2 [ NCBI-GEO ]   CCNB2 [ EBI - ARRAY_EXPRESS ]   CCNB2 [ SEEK ]   CCNB2 [ MEM ]
Gene Expression Viewer (FireBrowse)CCNB2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)9133
GTEX Portal (Tissue expression)CCNB2
Protein : pattern, domain, 3D structure
UniProt/SwissProtO95067   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtO95067  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProO95067
Splice isoforms : SwissVarO95067
PhosPhoSitePlusO95067
Domaine pattern : Prosite (Expaxy)CYCLINS (PS00292)   
Domains : Interpro (EBI)Cyclin-like    Cyclin_C-dom    Cyclin_N   
Domain families : Pfam (Sanger)Cyclin_C (PF02984)    Cyclin_N (PF00134)   
Domain families : Pfam (NCBI)pfam02984    pfam00134   
Domain families : Smart (EMBL)CYCLIN (SM00385)  
Conserved Domain (NCBI)CCNB2
DMDM Disease mutations9133
Blocks (Seattle)CCNB2
SuperfamilyO95067
Human Protein AtlasENSG00000157456
Peptide AtlasO95067
HPRD04131
IPIIPI00028266   
Protein Interaction databases
DIP (DOE-UCLA)O95067
IntAct (EBI)O95067
FunCoupENSG00000157456
BioGRIDCCNB2
STRING (EMBL)CCNB2
ZODIACCCNB2
Ontologies - Pathways
QuickGOO95067
Ontology : AmiGOG2/M transition of mitotic cell cycle  in utero embryonic development  cyclin-dependent protein serine/threonine kinase activity  protein binding  nucleoplasm  centrosome  cytosol  mitotic nuclear division  mitotic nuclear envelope disassembly  microtubule cytoskeleton  membrane  growth  T cell homeostasis  thymus development  cell division  regulation of cell cycle  
Ontology : EGO-EBIG2/M transition of mitotic cell cycle  in utero embryonic development  cyclin-dependent protein serine/threonine kinase activity  protein binding  nucleoplasm  centrosome  cytosol  mitotic nuclear division  mitotic nuclear envelope disassembly  microtubule cytoskeleton  membrane  growth  T cell homeostasis  thymus development  cell division  regulation of cell cycle  
Pathways : BIOCARTAEstrogen-responsive protein Efp controls cell cycle and breast tumors growth [Genes]   
Pathways : KEGGFoxO signaling pathway    Cell cycle    Oocyte meiosis    p53 signaling pathway    Progesterone-mediated oocyte maturation    HTLV-I infection   
NDEx NetworkCCNB2
Atlas of Cancer Signalling NetworkCCNB2
Wikipedia pathwaysCCNB2
Orthology - Evolution
OrthoDB9133
GeneTree (enSembl)ENSG00000157456
Phylogenetic Trees/Animal Genes : TreeFamCCNB2
HOVERGENO95067
HOGENOMO95067
Homologs : HomoloGeneCCNB2
Homology/Alignments : Family Browser (UCSC)CCNB2
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerCCNB2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)CCNB2
dbVarCCNB2
ClinVarCCNB2
1000_GenomesCCNB2 
Exome Variant ServerCCNB2
ExAC (Exome Aggregation Consortium)CCNB2 (select the gene name)
Genetic variants : HAPMAP9133
Genomic Variants (DGV)CCNB2 [DGVbeta]
DECIPHER (Syndromes)15:59397284-59417244  ENSG00000157456
CONAN: Copy Number AnalysisCCNB2 
Mutations
ICGC Data PortalCCNB2 
TCGA Data PortalCCNB2 
Broad Tumor PortalCCNB2
OASIS PortalCCNB2 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICCCNB2  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDCCNB2
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 CCNB2
DgiDB (Drug Gene Interaction Database)CCNB2
DoCM (Curated mutations)CCNB2 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)CCNB2 (select a term)
intoGenCCNB2
Cancer3DCCNB2(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM602755   
Orphanet
MedgenCCNB2
Genetic Testing Registry CCNB2
NextProtO95067 [Medical]
TSGene9133
GENETestsCCNB2
Huge Navigator CCNB2 [HugePedia]
snp3D : Map Gene to Disease9133
BioCentury BCIQCCNB2
ClinGenCCNB2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD9133
Chemical/Pharm GKB GenePA26148
Clinical trialCCNB2
Miscellaneous
canSAR (ICR)CCNB2 (select the gene name)
Probes
Litterature
PubMed59 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineCCNB2
EVEXCCNB2
GoPubMedCCNB2
iHOPCCNB2
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Thu Mar 30 14:55:26 CEST 2017

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