KEGG   Homo sapiens (human): 905
Entry
905               CDS       T01001                                 
Symbol
CCNT2, CYCT2
Name
(RefSeq) cyclin T2
  KO
K15188  cyclin T
Organism
hsa  Homo sapiens (human)
Pathway
hsa03250  Viral life cycle - HIV-1
hsa05202  Transcriptional misregulation in cancer
Network
nt06240  Transcription (cancer)
  Element
N00119  MLL-AF4 fusion to transcriptional activation
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09125 Information processing in viruses
   03250 Viral life cycle - HIV-1
    905 (CCNT2)
 09160 Human Diseases
  09161 Cancer: overview
   05202 Transcriptional misregulation in cancer
    905 (CCNT2)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03021 Transcription machinery [BR:hsa03021]
    905 (CCNT2)
Transcription machinery [BR:hsa03021]
 Eukaryotic type
  RNA polymerase II system
   Other transcription-related factors
    Super elongation complex (SEC)
     905 (CCNT2)
    Brd4/P-TEFb complex
     905 (CCNT2)
    7SK RNP complex
     905 (CCNT2)
SSDB
Motif
Pfam: CycT2-like_C Cyclin_N TFIIB
Other DBs
NCBI-GeneID: 905
NCBI-ProteinID: NP_490595
OMIM: 603862
HGNC: 1600
Ensembl: ENSG00000082258
UniProt: O60583 B4DH21
Structure
Position
2:134918822..134959342
AA seq 730 aa
MASGRGASSRWFFTREQLENTPSRRCGVEADKELSCRQQAANLIQEMGQRLNVSQLTINT
AIVYMHRFYMHHSFTKFNKNIISSTALFLAAKVEEQARKLEHVIKVAHACLHPLEPLLDT
KCDAYLQQTQELVILETIMLQTLGFEITIEHPHTDVVKCTQLVRASKDLAQTSYFMATNS
LHLTTFCLQYKPTVIACVCIHLACKWSNWEIPVSTDGKHWWEYVDPTVTLELLDELTHEF
LQILEKTPNRLKKIRNWRANQAARKPKVDGQVSETPLLGSSLVQNSILVDSVTGVPTNPS
FQKPSTSAFPAPVPLNSGNISVQDSHTSDNLSMLATGMPSTSYGLSSHQEWPQHQDSART
EQLYSQKQETSLSGSQYNINFQQGPSISLHSGLHHRPDKISDHSSVKQEYTHKAGSSKHH
GPISTTPGIIPQKMSLDKYREKRKLETLDLDVRDHYIAAQVEQQHKQGQSQAASSSSVTS
PIKMKIPIANTEKYMADKKEKSGSLKLRIPIPPTDKSASKEELKMKIKVSSSERHSSSDE
GSGKSKHSSPHISRDHKEKHKEHPSSRHHTSSHKHSHSHSGSSSGGSKHSADGIPPTVLR
SPVGLSSDGISSSSSSSRKRLHVNDASHNHHSKMSKSSKSSGSSSSSSSSVKQYISSHNS
VFNHPLPPPPPVTYQVGYGHLSTLVKLDKKPVETNGPDANHEYSTSSQHMDYKDTFDMLD
SLLSAQGMNM
NT seq 2193 nt   +upstreamnt  +downstreamnt
atggcgtcgggccgtggagcttcttctcgctggttctttactcgggaacagctggagaac
acgccgagccgccgctgcggagtggaggcggataaagagctctcgtgccgccagcaggcg
gccaacctcatccaggagatgggacagcgtctcaatgtctctcagcttacaataaacact
gcgattgtttatatgcacaggttttatatgcaccattctttcaccaaattcaacaaaaat
ataatatcgtctactgcattatttttggctgcaaaagtggaagaacaggctcgaaaactt
gaacatgttatcaaagtagcacatgcttgtcttcatcctctagagccactgctggatact
aaatgtgatgcttaccttcaacagactcaagaactggttatacttgaaaccataatgcta
caaactctaggttttgagatcaccattgaacacccacacacagatgtggtgaaatgtacc
cagttagtaagagcaagcaaggatttggcacagacatcctatttcatggctaccaacagt
ctgcatcttacaaccttctgtcttcagtacaaaccaacagtgatagcatgtgtatgcatt
catttggcttgcaaatggtccaattgggagatccctgtatcaactgatggaaagcattgg
tgggaatatgtggatcctacagttactctagaattattagatgagctaacacatgagttt
ctacaaatattggagaaaacgcctaataggttgaagaagattcgaaactggagggctaat
caggcagctaggaaaccaaaagtagatggacaggtatcagagacaccacttcttggttca
tctttggtccagaattccattttagtagatagtgtcactggtgtgcctacaaacccaagt
tttcagaaaccatctacatcagcattccctgcgccagtacctctaaattcaggaaatatt
tctgttcaagacagccatacatctgataatttgtcaatgctagcaacaggaatgccaagt
acttcatacggtttatcatcacaccaggaatggcctcaacatcaagactcagcaaggaca
gaacagctatattcacagaaacaggagacatctttgtctggtagccagtacaacatcaac
ttccagcagggaccttctatatcactgcattcaggattacatcacagacctgacaaaatt
tcagatcattcttctgttaagcaagaatatactcataaagcagggagcagtaaacaccat
gggccaatttccactactccaggaataattcctcagaaaatgtctttagataaatataga
gaaaagcgtaaactagaaactcttgatctcgatgtaagggatcattatatagctgcccag
gtagaacagcagcacaaacaagggcagtcacaggcagccagcagcagttctgttacttct
cccattaaaatgaaaatacctatcgcaaatactgaaaaatacatggcagacaaaaaggaa
aagagtgggtcactgaaattacggattccaataccacccactgataaaagcgccagtaaa
gaagaactgaaaatgaaaataaaagtttcttcttcagaaagacacagctcttctgatgaa
ggcagtgggaagagcaaacattcaagcccacatattagcagagaccataaggagaagcac
aaggagcatccttcaagccgccaccacaccagcagccacaagcattcccactcgcatagt
ggcagcagcagcggtggcagtaaacacagtgccgacggaataccacccactgttctgagg
agtcctgttggcctgagcagtgatggcatttcctctagctccagctcttcaaggaagagg
ctgcatgtcaatgatgcatctcacaaccaccactccaaaatgagcaaaagttccaaaagt
tcaggtagttcatctagttcttcctcctctgttaagcagtatatatcctctcacaactct
gtttttaaccatcccttaccccctcctccccctgtcacataccaggtgggctacggacat
ctcagcaccctcgtgaaactggacaagaagccagtggagaccaacggtcctgatgccaat
cacgagtacagtacaagcagccagcatatggactacaaagacacattcgacatgctggac
tcactgttaagtgcccaaggaatgaacatgtaa

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Ontology (2)   
   KEGG BRITE (2)   
Pathway (2)   
   KEGG PATHWAY (2)   
Network (2)   
   KEGG NETWORK (2)   
Disease (1)   
   OMIM (1)   
Genome (1)   
   KEGG GENOME (1)   
Gene (22)   
   KEGG ORTHOLOGY (1)   
   RefGene (15)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (1)   
   OC (1)   
Protein sequence (15)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (12)   
DNA sequence (34)   
   RefSeq(nuc) (14)   
   GenBank (10)   
   EMBL (10)   
3D Structure (1)   
   PDB (1)   
Protein domain (3)   
   Pfam (3)   
All databases (83)   

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