KEGG   Homo sapiens (human): 8626
Entry
8626              CDS       T01001                                 
Symbol
TP63, AIS, B(p51A), B(p51B), EEC3, KET, LMS, NBP, OFC8, RHS, SHFM4, TP53CP, TP53L, TP73L, p40, p51, p53CP, p63, p73H, p73L
Name
(RefSeq) tumor protein p63
  KO
K10149  tumor protein p63
Organism
hsa  Homo sapiens (human)
Pathway
hsa05206  MicroRNAs in cancer
Disease
H00471  Split-hand/foot malformation
H00516  Cleft lip and/or cleft palate
H00627  Premature ovarian failure
H00638  Ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome
H00640  Limb-mammary syndrome
H00641  ADULT syndrome
H00752  Ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome and Rapp-Hodgkin syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09160 Human Diseases
  09161 Cancer: overview
   05206 MicroRNAs in cancer
    8626 (TP63)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    8626 (TP63)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  beta-Scaffold factors with minor groove contacts
   p53
    8626 (TP63)
SSDB
Motif
Pfam: P53 P53_tetramer SAM_2
Other DBs
NCBI-GeneID: 8626
NCBI-ProteinID: NP_003713
OMIM: 603273
HGNC: 15979
Ensembl: ENSG00000073282
UniProt: Q9H3D4 A0A0S2Z4N5
Structure
Position
3:189596746..189897276
AA seq 680 aa
MNFETSRCATLQYCPDPYIQRFVETPAHFSWKESYYRSTMSQSTQTNEFLSPEVFQHIWD
FLEQPICSVQPIDLNFVDEPSEDGATNKIEISMDCIRMQDSDLSDPMWPQYTNLGLLNSM
DQQIQNGSSSTSPYNTDHAQNSVTAPSPYAQPSSTFDALSPSPAIPSNTDYPGPHSFDVS
FQQSSTAKSATWTYSTELKKLYCQIAKTCPIQIKVMTPPPQGAVIRAMPVYKKAEHVTEV
VKRCPNHELSREFNEGQIAPPSHLIRVEGNSHAQYVEDPITGRQSVLVPYEPPQVGTEFT
TVLYNFMCNSSCVGGMNRRPILIIVTLETRDGQVLGRRCFEARICACPGRDRKADEDSIR
KQQVSDSTKNGDGTKRPFRQNTHGIQMTSIKKRRSPDDELLYLPVRGRETYEMLLKIKES
LELMQYLPQHTIETYRQQQQQQHQHLLQKQTSIQSPSSYGNSSPPLNKMNSMNKLPSVSQ
LINPQQRNALTPTTIPDGMGANIPMMGTHMPMAGDMNGLSPTQALPPPLSMPSTSHCTPP
PPYPTDCSIVSFLARLGCSSCLDYFTTQGLTTIYQIEHYSMDDLASLKIPEQFRHAIWKG
ILDHRQLHEFSSPSHLLRTPSSASTVSVGSSETRGERVIDAVRFTLRQTISFPPRDEWND
FNFDMDARRNKQQRIKEEGE
NT seq 2043 nt   +upstreamnt  +downstreamnt
atgaattttgaaacttcacggtgtgccaccctacagtactgccctgacccttacatccag
cgtttcgtagaaaccccagctcatttctcttggaaagaaagttattaccgatccaccatg
tcccagagcacacagacaaatgaattcctcagtccagaggttttccagcatatctgggat
tttctggaacagcctatatgttcagttcagcccattgacttgaactttgtggatgaacca
tcagaagatggtgcgacaaacaagattgagattagcatggactgtatccgcatgcaggac
tcggacctgagtgaccccatgtggccacagtacacgaacctggggctcctgaacagcatg
gaccagcagattcagaacggctcctcgtccaccagtccctataacacagaccacgcgcag
aacagcgtcacggcgccctcgccctacgcacagcccagctccaccttcgatgctctctct
ccatcacccgccatcccctccaacaccgactacccaggcccgcacagtttcgacgtgtcc
ttccagcagtcgagcaccgccaagtcggccacctggacgtattccactgaactgaagaaa
ctctactgccaaattgcaaagacatgccccatccagatcaaggtgatgaccccacctcct
cagggagctgttatccgcgccatgcctgtctacaaaaaagctgagcacgtcacggaggtg
gtgaagcggtgccccaaccatgagctgagccgtgaattcaacgagggacagattgcccct
cctagtcatttgattcgagtagaggggaacagccatgcccagtatgtagaagatcccatc
acaggaagacagagtgtgctggtaccttatgagccaccccaggttggcactgaattcacg
acagtcttgtacaatttcatgtgtaacagcagttgtgttggagggatgaaccgccgtcca
attttaatcattgttactctggaaaccagagatgggcaagtcctgggccgacgctgcttt
gaggcccggatctgtgcttgcccaggaagagacaggaaggcggatgaagatagcatcaga
aagcagcaagtttcggacagtacaaagaacggtgatggtacgaagcgcccgtttcgtcag
aacacacatggtatccagatgacatccatcaagaaacgaagatccccagatgatgaactg
ttatacttaccagtgaggggccgtgagacttatgaaatgctgttgaagatcaaagagtcc
ctggaactcatgcagtaccttcctcagcacacaattgaaacgtacaggcaacagcaacag
cagcagcaccagcacttacttcagaaacagacctcaatacagtctccatcttcatatggt
aacagctccccacctctgaacaaaatgaacagcatgaacaagctgccttctgtgagccag
cttatcaaccctcagcagcgcaacgccctcactcctacaaccattcctgatggcatggga
gccaacattcccatgatgggcacccacatgccaatggctggagacatgaatggactcagc
cccacccaggcactccctcccccactctccatgccatccacctcccactgcacaccccca
cctccgtatcccacagattgcagcattgtcagtttcttagcgaggttgggctgttcatca
tgtctggactatttcacgacccaggggctgaccaccatctatcagattgagcattactcc
atggatgatctggcaagtctgaaaatccctgagcaatttcgacatgcgatctggaagggc
atcctggaccaccggcagctccacgaattctcctccccttctcatctcctgcggacccca
agcagtgcctctacagtcagtgtgggctccagtgagacccggggtgagcgtgttattgat
gctgtgcgattcaccctccgccagaccatctctttcccaccccgagatgagtggaatgac
ttcaactttgacatggatgctcgccgcaataagcaacagcgcatcaaagaggagggggag
tga

  All links  
Disease (9)   
   OMIM (9)   
Gene (16)   
   RefGene (6)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (5)   
   OC (1)   
Protein sequence (16)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (13)   
DNA sequence (61)   
   RefSeq(nuc) (13)   
   GenBank (24)   
   EMBL (24)   
3D Structure (28)   
   PDB (28)   
Protein domain (3)   
   Pfam (3)   
All databases (133)   

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