Homo sapiens (human): 9133
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Entry
9133 CDS
T01001
Symbol
CCNB2, HsT17299
Name
(RefSeq) cyclin B2
KO
K21770
G2/mitotic-specific cyclin-B2
Organism
hsa
Homo sapiens (human)
Pathway
hsa04068
FoxO signaling pathway
hsa04110
Cell cycle
hsa04114
Oocyte meiosis
hsa04115
p53 signaling pathway
hsa04218
Cellular senescence
hsa04914
Progesterone-mediated oocyte maturation
hsa05166
Human T-cell leukemia virus 1 infection
hsa05170
Human immunodeficiency virus 1 infection
Network
nt06160
Human T-cell leukemia virus 1 (HTLV-1)
nt06161
Human immunodeficiency virus 1 (HIV-1)
nt06230
Cell cycle (cancer)
Element
N00455
CDC25-Cell cycle G2/M
N00456
HIV Vpr to CDC25-cell cycle G2M
N00457
HIV Vpr to cell cycle G2M
N00459
WEE1-Cell cycle G2/M
N00460
HIV Vpr to WEE1-cell cycle G2M
N00499
ATR-p21-Cell cycle G2/M
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04068 FoxO signaling pathway
9133 (CCNB2)
09160 Human Diseases
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
9133 (CCNB2)
05170 Human immunodeficiency virus 1 infection
9133 (CCNB2)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03032 DNA replication proteins [BR:
hsa03032
]
9133 (CCNB2)
03036 Chromosome and associated proteins [BR:
hsa03036
]
9133 (CCNB2)
DNA replication proteins [BR:
hsa03032
]
Eukaryotic type
DNA Replication Termination Factors
Prevention of re-replication factors
9133 (CCNB2)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Centrosome formation proteins
Cyclins
9133 (CCNB2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Cyclin_N
Cyclin_C
Motif
Other DBs
NCBI-GeneID:
9133
NCBI-ProteinID:
NP_004692
OMIM:
602755
HGNC:
1580
Ensembl:
ENSG00000157456
UniProt:
O95067
LinkDB
All DBs
Position
15:59105146..59125045
Genome browser
AA seq
398 aa
AA seq
DB search
MALLRRPTVSSDLENIDTGVNSKVKSHVTIRRTVLEEIGNRVTTRAAQVAKKAQNTKVPV
QPTKTTNVNKQLKPTASVKPVQMEKLAPKGPSPTPEDVSMKEENLCQAFSDALLCKIEDI
DNEDWENPQLCSDYVKDIYQYLRQLEVLQSINPHFLDGRDINGRMRAILVDWLVQVHSKF
RLLQETLYMCVGIMDRFLQVQPVSRKKLQLVGITALLLASKYEEMFSPNIEDFVYITDNA
YTSSQIREMETLILKELKFELGRPLPLHFLRRASKAGEVDVEQHTLAKYLMELTLIDYDM
VHYHPSKVAAAASCLSQKVLGQGKWNLKQQYYTGYTENEVLEVMQHMAKNVVKVNENLTK
FIAIKNKYASSKLLKISMIPQLNSKAVKDLASPLIGRS
NT seq
1197 nt
NT seq
+upstream
nt +downstream
nt
atggcgctgctccgacgcccgacggtgtccagtgatttggagaatattgacacaggagtt
aattctaaagttaagagtcatgtgactattaggcgaactgttttagaagaaattggaaat
agagttacaaccagagcagcacaagtagctaagaaagctcagaacaccaaagttccagtt
caacccaccaaaacaacaaatgtcaacaaacaactgaaacctactgcttctgtcaaacca
gtacagatggaaaagttggctccaaagggtccttctcccacacctgaggatgtctccatg
aaggaagagaatctctgccaagctttttctgatgccttgctctgcaaaatcgaggacatt
gataacgaagattgggagaaccctcagctctgcagtgactacgttaaggatatctatcag
tatctcaggcagctggaggttttgcagtccataaacccacatttcttagatggaagagat
ataaatggacgcatgcgtgccatcctagtggattggctggtacaagtccactccaagttt
aggcttctgcaggagactctgtacatgtgcgttggcattatggatcgatttttacaggtt
cagccagtttcccggaagaagcttcaattagttgggattactgctctgctcttggcttcc
aagtatgaggagatgttttctccaaatattgaagactttgtttacatcacagacaatgct
tataccagttcccaaatccgagaaatggaaactctaattttgaaagaattgaaatttgag
ttgggtcgacccttgccactacacttcttaaggcgagcatcaaaagccggggaggttgat
gttgaacagcacactttagccaagtatttgatggagctgactctcatcgactatgatatg
gtgcattatcatccttctaaggtagcagcagctgcttcctgcttgtctcagaaggttcta
ggacaaggaaaatggaacttaaagcagcagtattacacaggatacacagagaatgaagta
ttggaagtcatgcagcacatggccaagaatgtggtgaaagtaaatgaaaacttaactaaa
ttcatcgccatcaagaataagtatgcaagcagcaaactcctgaagatcagcatgatccct
cagctgaactcaaaagccgtcaaagaccttgcctccccactgataggaaggtcctag
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