Pan paniscus (bonobo): 100968381 Help Entry 100968381         CDS       T02283                                  Symbol TP73 Name (RefSeq) tumor protein p73 isoform X2   KO K10148   tumor protein p73 Organism pps  Pan paniscus (bonobo) Pathway pps04115   p53 signaling pathway pps04390   Hippo signaling pathway pps04722   Neurotrophin signaling pathway pps05162   Measles Brite KEGG Orthology (KO) [BR:pps00001]  09130 Environmental Information Processing   09132 Signal transduction    04390 Hippo signaling pathway     100968381 (TP73)  09140 Cellular Processes   09143 Cell growth and death    04115 p53 signaling pathway     100968381 (TP73)  09150 Organismal Systems   09156 Nervous system    04722 Neurotrophin signaling pathway     100968381 (TP73)  09160 Human Diseases   09172 Infectious disease: viral    05162 Measles     100968381 (TP73)  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03000 Transcription factors [BR:pps03000]     100968381 (TP73) Transcription factors [BR:pps03000]  Eukaryotic type   beta-Scaffold factors with minor groove contacts    p53     100968381 (TP73) BRITE hierarchy SSDB OrthologParalogGFIT Motif Pfam:  P53 P53_tetramer SAM_2 SAM_1 Motif Other DBs NCBI-GeneID:  100968381 NCBI-ProteinID:  XP_008969003 Ensembl:  ENSPPAG00000036965 UniProt:  A0A2R9BEG2 LinkDB All DBs Position 1:complement(224577312..224657001) Genome browser AA seq 587 aa AA seqDB search MLYVGDPARHLATAQFNLLSSTMDQMSSRAASASPYTPEHAASVPTHSPYAQPSSTFDTM SPAPVIPSNTDYPGPHHFEVTFQQSSTAKSATWTYSPLLKKLYCQIAKTCPIQIKVSTPP PPGTAIRAMPVYKKAEHVTDVVKRCPNHELGRDFNEGQSAPASHLIRVEGNNLSQYVDDP VTGRQSVVVPYEPPQVGTEFTTILYNFMCNSSCVGGMNRRPILIIITLEMRDGQVLGRRS FEGRICACPGRDRKADEDHYREQQALNESSAKNGAASKRAFKQSPPAVPALGAGVKKRRH GDEDTYYLQVRGRENFEILMKLKESLELMELVPQPLVDSYRQQQQLLQRPSHLQPPSYGP VLSPMNKVHGGMNKLPSVNQLVGQPPPHSSAATPNLGPVGPGMLNNHGHAVPANGEMSSS HSAQSMVSGSHCTPPPPYHADPSLVSFLTGLGCPNCIEYFTSQGLQSIYHLQNLTIEDLG ALKIPEQYRMTIWRGLQDLKQGHDYSTTQQLLRSSNAATISIGGSGELQRQRVMEAVHFR VRHTITIPNRGGPGGGPDEWADFGFDLPDCKARKQPIKEEFTEAEIH NT seq 1764 nt NT seq  +upstreamnt  +downstreamnt atgctgtacgtcggtgaccccgcacggcacctcgccacggcccagttcaatctgctgagc agcaccatggaccagatgagcagccgcgcggcctcggccagtccctacaccccagagcac gccgccagcgtgcccacccactcgccctacgcacagcccagctccaccttcgacaccatg tcgccggcgcctgtcatcccctccaacaccgactaccccggcccccaccacttcgaggtc actttccagcagtccagcacggccaagtcagccacctggacgtactccccgctcttgaag aaactctactgccagatcgccaagacatgccccatccagatcaaggtgtccaccccgcca cccccaggcaccgccatccgggccatgcctgtttacaagaaagcggagcacgtgaccgac gtcgtgaaacgctgccccaaccatgagctcgggagggacttcaacgaaggacagtctgct ccagccagccacctcatccgcgtggaaggcaataatctctcgcagtatgtggatgaccct gtcacgggcaggcagagcgtcgtggtgccctatgagccaccacaggtggggacggaattc accaccatcctgtacaacttcatgtgtaacagcagctgtgtagggggcatgaaccggcgg cccatcctcatcatcatcaccctggagatgcgggatgggcaggtgctgggccgccggtcc tttgagggccgcatctgcgcctgtcctggccgcgaccgaaaagccgatgaggaccactac cgggagcagcaggccctgaacgaaagctccgccaagaacggggccgccagcaagcgtgcc ttcaagcagagcccccctgccgtccccgcccttggcgctggcgtgaagaagcggcggcat ggagacgaggacacgtactacctgcaggtgcgaggccgggagaactttgagatcctgatg aagctgaaagagagcctggagctgatggagttggtgccgcagccactggtggactcctat cggcagcagcagcagctcctacagaggccgagtcacctacagcccccgtcctacgggccg gtcctctcgcccatgaacaaggtgcacgggggcatgaacaagctgccctccgtcaaccag ctggtgggccagcctcccccgcacagttcggcagctacacccaacctggggcccgtgggc cctgggatgctcaacaaccatggccacgcagtgccagccaacggcgagatgagcagcagc cacagcgcccagtccatggtctcggggtcccactgcactccgccacccccgtaccacgcc gaccccagcctcgtcagttttttaacaggattggggtgtccaaactgcatcgagtatttc acctcccaagggttacagagcatttaccacctgcagaacctgaccattgaggacctgggg gccctgaagatccccgagcagtaccgcatgaccatctggcggggcctgcaggacctgaag cagggccacgactacagcaccacgcagcagctgctccgctccagcaacgcggccaccatc tccatcggcggctcaggggaactgcagcgccagcgggtcatggaggccgtgcacttccgc gtgcgccacaccatcaccatccccaaccgcggcggcccaggcggcggccctgacgagtgg gcagactttggcttcgacctgcccgactgcaaggcccgcaagcagcccatcaaggaggag ttcacggaggccgagatccattga

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