KEGG   Homo sapiens (human): 5090
Entry
5090              CDS       T01001                                 
Symbol
PBX3
Name
(RefSeq) PBX homeobox 3
  KO
K15610  pre-B-cell leukemia transcription factor 3
Organism
hsa  Homo sapiens (human)
Pathway
hsa05202  Transcriptional misregulation in cancer
Network
nt06240  Transcription (cancer)
  Element
N00119  MLL-AF4 fusion to transcriptional activation
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09160 Human Diseases
  09161 Cancer: overview
   05202 Transcriptional misregulation in cancer
    5090 (PBX3)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    5090 (PBX3)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Helix-turn-helix
   Homeo domain TALE
    5090 (PBX3)
SSDB
Motif
Pfam: PBC Homeobox_KN Homeodomain LZ3wCH DUF7260 UCH TOG_MAP3K1 DptA
Other DBs
NCBI-GeneID: 5090
NCBI-ProteinID: NP_006186
OMIM: 176312
HGNC: 8634
Ensembl: ENSG00000167081
UniProt: P40426 Q96AL5
Position
9:125747373..125967377
AA seq 434 aa
MDDQSRMLQTLAGVNLAGHSVQGGMALPPPPHGHEGADGDGRKQDIGDILHQIMTITDQS
LDEAQAKKHALNCHRMKPALFSVLCEIKEKTGLSIRGAQEEDPPDPQLMRLDNMLLAEGV
SGPEKGGGSAAAAAAAAASGGSSDNSIEHSDYRAKLTQIRQIYHTELEKYEQACNEFTTH
VMNLLREQSRTRPISPKEIERMVGIIHRKFSSIQMQLKQSTCEAVMILRSRFLDARRKRR
NFSKQATEILNEYFYSHLSNPYPSEEAKEELAKKCSITVSQVSNWFGNKRIRYKKNIGKF
QEEANLYAAKTAVTAAHAVAAAVQNNQTNSPTTPNSGSSGSFNLPNSGDMFMNMQSLNGD
SYQGSQVGANVQSQVDTLRHVINQTGGYSDGLGGNSLYSPHNLNANGGWQDATTPSSVTS
PTEGPGSVHSDTSN
NT seq 1305 nt   +upstreamnt  +downstreamnt
atggacgatcaatccaggatgctgcagactctggccggggtgaacctggctggccactcg
gtgcaggggggcatggccctgccgcctcccccgcacggccacgaaggggcggacggcgac
ggcaggaagcaggacatcggcgacatcctccaccagatcatgaccatcaccgaccagagc
ttggacgaggcgcaagcaaagaaacatgccctgaactgtcacagaatgaaaccagcgctc
ttcagcgtcctgtgtgagatcaaagagaaaacaggtctcagcatcagaggagcccaggag
gaggaccctcccgatccccagctaatgagactggacaatatgcttttggcagaaggggtt
tcaggtcctgagaaaggtgggggatcggcggcagcagctgcagccgcggcagcctctgga
ggttcttcagataactctattgaacactcagattacagagccaaattgacccagatcaga
caaatctatcacacagaactggagaaatatgaacaggcatgtaatgaatttactacacat
gtgatgaaccttctccgagaacagagtagaacacgtcccatttctccaaaagagattgaa
agaatggtgggcatcatccatcgaaaatttagttccattcagatgcagctcaaacaaagc
acttgtgaagcagttatgattttaagatcaaggttccttgatgccagacggaaaaggcgt
aacttcagtaaacaggccacagaaatcttgaatgaatatttttactcacacctcagcaac
ccctaccccagtgaagaagccaaagaggagctggccaagaaatgcagcatcacagtgtca
caggtatccaattggtttggcaacaaacgaatcaggtacaagaagaacattggcaagttt
caggaagaagccaacctctatgctgcaaagacggccgtgacagctgcacacgcagtagca
gcagctgtgcagaacaaccagaccaattcgcccaccacaccaaattccggttcttctggt
tcttttaacctcccaaattctggggacatgttcatgaacatgcagagtctgaatggggat
tcttaccaagggtcccaagtcggagccaatgtgcaatcacaggtggataccctccgtcat
gttatcaatcagacgggaggctacagtgatggccttggaggaaattcactgtacagtcca
cataatttaaatgctaatggaggctggcaggacgcaacaactccatcttctgtgacttct
cctacagaaggcccaggaagtgtgcactcggatacctctaactaa

  All links  
Disease (1)   
   OMIM (1)   
Gene (18)   
   RefGene (9)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (4)   
   OC (1)   
Protein sequence (17)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (14)   
DNA sequence (52)   
   RefSeq(nuc) (16)   
   GenBank (18)   
   EMBL (18)   
Protein domain (6)   
   Pfam (6)   
All databases (94)   

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