Homo sapiens (human): 7161
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Entry
7161 CDS
T01001
Symbol
TP73, CILD47, P73
Name
(RefSeq) tumor protein p73
KO
K10148
tumor protein p73
Organism
hsa
Homo sapiens (human)
Pathway
hsa04115
p53 signaling pathway
hsa04390
Hippo signaling pathway
hsa04722
Neurotrophin signaling pathway
hsa05162
Measles
Network
nt06169
Measles virus (MV)
Element
N00695
MV V to p73-mediated transcription
Disease
H00564
Primary ciliary dyskinesia
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04390 Hippo signaling pathway
7161 (TP73)
09140 Cellular Processes
09143 Cell growth and death
04115 p53 signaling pathway
7161 (TP73)
09150 Organismal Systems
09156 Nervous system
04722 Neurotrophin signaling pathway
7161 (TP73)
09160 Human Diseases
09172 Infectious disease: viral
05162 Measles
7161 (TP73)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
7161 (TP73)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
beta-Scaffold factors with minor groove contacts
p53
7161 (TP73)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
P53
P53_tetramer
SAM_2
SAM_1
Motif
Other DBs
NCBI-GeneID:
7161
NCBI-ProteinID:
NP_005418
OMIM:
601990
HGNC:
12003
Ensembl:
ENSG00000078900
UniProt:
O15350
Structure
PDB
PDBj
LinkDB
All DBs
Position
1:3652516..3736201
Genome browser
AA seq
636 aa
AA seq
DB search
MAQSTATSPDGGTTFEHLWSSLEPDSTYFDLPQSSRGNNEVVGGTDSSMDVFHLEGMTTS
VMAQFNLLSSTMDQMSSRAASASPYTPEHAASVPTHSPYAQPSSTFDTMSPAPVIPSNTD
YPGPHHFEVTFQQSSTAKSATWTYSPLLKKLYCQIAKTCPIQIKVSTPPPPGTAIRAMPV
YKKAEHVTDVVKRCPNHELGRDFNEGQSAPASHLIRVEGNNLSQYVDDPVTGRQSVVVPY
EPPQVGTEFTTILYNFMCNSSCVGGMNRRPILIIITLEMRDGQVLGRRSFEGRICACPGR
DRKADEDHYREQQALNESSAKNGAASKRAFKQSPPAVPALGAGVKKRRHGDEDTYYLQVR
GRENFEILMKLKESLELMELVPQPLVDSYRQQQQLLQRPSHLQPPSYGPVLSPMNKVHGG
MNKLPSVNQLVGQPPPHSSAATPNLGPVGPGMLNNHGHAVPANGEMSSSHSAQSMVSGSH
CTPPPPYHADPSLVSFLTGLGCPNCIEYFTSQGLQSIYHLQNLTIEDLGALKIPEQYRMT
IWRGLQDLKQGHDYSTAQQLLRSSNAATISIGGSGELQRQRVMEAVHFRVRHTITIPNRG
GPGGGPDEWADFGFDLPDCKARKQPIKEEFTEAEIH
NT seq
1911 nt
NT seq
+upstream
nt +downstream
nt
atggcccagtccaccgccacctcccctgatgggggcaccacgtttgagcacctctggagc
tctctggaaccagacagcacctacttcgaccttccccagtcaagccgggggaataatgag
gtggtgggcggaacggattccagcatggacgtcttccacctggagggcatgactacatct
gtcatggcccagttcaatctgctgagcagcaccatggaccagatgagcagccgcgcggcc
tcggccagcccctacaccccagagcacgccgccagcgtgcccacccactcgccctacgca
caacccagctccaccttcgacaccatgtcgccggcgcctgtcatcccctccaacaccgac
taccccggaccccaccactttgaggtcactttccagcagtccagcacggccaagtcagcc
acctggacgtactccccgctcttgaagaaactctactgccagatcgccaagacatgcccc
atccagatcaaggtgtccaccccgccacccccaggcaccgccatccgggccatgcctgtt
tacaagaaagcggagcacgtgaccgacgtcgtgaaacgctgccccaaccacgagctcggg
agggacttcaacgaaggacagtctgctccagccagccacctcatccgcgtggaaggcaat
aatctctcgcagtatgtggatgaccctgtcaccggcaggcagagcgtcgtggtgccctat
gagccaccacaggtggggacggaattcaccaccatcctgtacaacttcatgtgtaacagc
agctgtgtagggggcatgaaccggcggcccatcctcatcatcatcaccctggagatgcgg
gatgggcaggtgctgggccgccggtcctttgagggccgcatctgcgcctgtcctggccgc
gaccgaaaagctgatgaggaccactaccgggagcagcaggccctgaacgagagctccgcc
aagaacggggccgccagcaagcgtgccttcaagcagagcccccctgccgtccccgccctt
ggtgccggtgtgaagaagcggcggcatggagacgaggacacgtactaccttcaggtgcga
ggccgggagaactttgagatcctgatgaagctgaaagagagcctggagctgatggagttg
gtgccgcagccactggtggactcctatcggcagcagcagcagctcctacagaggccgagt
cacctacagcccccgtcctacgggccggtcctctcgcccatgaacaaggtgcacgggggc
atgaacaagctgccctccgtcaaccagctggtgggccagcctcccccgcacagttcggca
gctacacccaacctggggcccgtgggccccgggatgctcaacaaccatggccacgcagtg
ccagccaacggcgagatgagcagcagccacagcgcccagtccatggtctcggggtcccac
tgcactccgccacccccctaccacgccgaccccagcctcgtcagttttttaacaggattg
gggtgtccaaactgcatcgagtatttcacctcccaagggttacagagcatttaccacctg
cagaacctgaccattgaggacctgggggccctgaagatccccgagcagtaccgcatgacc
atctggcggggcctgcaggacctgaagcagggccacgactacagcaccgcgcagcagctg
ctccgctctagcaacgcggccaccatctccatcggcggctcaggggaactgcagcgccag
cgggtcatggaggccgtgcacttccgcgtgcgccacaccatcaccatccccaaccgcggc
ggcccaggcggcggccctgacgagtgggcggacttcggcttcgacctgcccgactgcaag
gcccgcaagcagcccatcaaggaggagttcacggaggccgagatccactga
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