Entry |
|
Symbol |
PBX1, CAKUHED
|
Name |
|
KO |
K09355 | pre-B-cell leukemia transcription factor 1 |
|
Organism |
|
Pathway |
hsa04927 | Cortisol synthesis and secretion |
hsa05202 | Transcriptional misregulation in cancer |
|
Network |
|
Element |
N00117 | E2A-PBX1 fusion to transcriptional activation |
N00297 | ACTH-cortisol signaling pathway |
N00298 | CYP11B1-CYP11B2 fusion to ACTH-cortisol signaling pathway |
N00320 | Mutation-activated PRKACA to ACTH-cortisol signaling pathway |
N00321 | Mutation-activated GNAS to ACTH-cortisol signaling pathway |
N00322 | Mutation-inactivated PRKAR1A to ACTH-cortisol signaling pathway |
N00323 | Mutation-inactivated PDE11A/PDE8B to ACTH-cortisol signaling pathway |
N01778 | Production of IL10 via the Sirtuin1 signaling cascade |
|
Disease |
H00001 | B-cell acute lymphoblastic leukemia |
H01867 | Congenital anomalies of kidney and urinary tract |
|
Brite |
KEGG Orthology (KO) [BR:hsa00001]
09140 Cellular Processes
09141 Transport and catabolism
04148 Efferocytosis
5087 (PBX1)
09150 Organismal Systems
09152 Endocrine system
04927 Cortisol synthesis and secretion
5087 (PBX1)
09160 Human Diseases
09161 Cancer: overview
05202 Transcriptional misregulation in cancer
5087 (PBX1)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
5087 (PBX1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:hsa03000]
5087 (PBX1)
Transcription factors [BR:hsa03000]
Eukaryotic type
Helix-turn-helix
Homeo domain TALE
5087 (PBX1)
|
SSDB |
|
Motif |
|
Other DBs |
|
Structure |
|
LinkDB |
|
Position |
1:164559184..164886047
|
AA seq |
430 aa
MDEQPRLMHSHAGVGMAGHPGLSQHLQDGAGGTEGEGGRKQDIGDILQQIMTITDQSLDE
AQARKHALNCHRMKPALFNVLCEIKEKTVLSIRGAQEEEPTDPQLMRLDNMLLAEGVAGP
EKGGGSAAAAAAAAASGGAGSDNSVEHSDYRAKLSQIRQIYHTELEKYEQACNEFTTHVM
NLLREQSRTRPISPKEIERMVSIIHRKFSSIQMQLKQSTCEAVMILRSRFLDARRKRRNF
NKQATEILNEYFYSHLSNPYPSEEAKEELAKKCGITVSQVSNWFGNKRIRYKKNIGKFQE
EANIYAAKTAVTATNVSAHGSQANSPSTPNSAGSSSSFNMSNSGDLFMSVQSLNGDSYQG
AQVGANVQSQVDTLRHVISQTGGYSDGLAASQMYSPQGISANGGWQDATTPSSVTSPTEG
PGSVHSDTSN |
NT seq |
1293 nt +upstreamnt +downstreamnt
atggacgagcagcccaggctgatgcattcccatgctggggtcgggatggccggacacccc
ggcctgtcccagcacttgcaggatggggccggagggaccgagggggagggcgggaggaag
caggacattggagacattttacagcaaattatgaccatcacagaccagagtttggatgag
gcgcaggccagaaaacatgctttaaactgccacagaatgaagcctgccttgtttaatgtg
ttgtgtgaaatcaaagaaaaaacagttttgagtatccgaggagcccaggaggaggaaccc
acagacccccagctgatgcggctggacaacatgctgttagcggaaggcgtggcggggcct
gagaagggcggagggtcggcggcagcggcggcagcggcggcggcttctggaggggcaggt
tcagacaactcagtggagcattcagattacagagccaaactctcacagatcagacaaatc
taccatacggagctggagaaatacgagcaggcctgcaacgagttcaccacccacgtgatg
aatctcctgcgagagcaaagccggaccaggcccatctccccaaaggagattgagcggatg
gtcagcatcatccaccgcaagttcagctccatccagatgcagctcaagcagagcacgtgc
gaggcggtgatgatcctgcgttcccgatttctggatgcgcggcggaagagacggaatttc
aacaagcaagcgacagaaatcctgaatgaatatttctattcccatctcagcaacccttac
cccagtgaggaagccaaagaggagttagccaagaagtgtggcatcacagtctcccaggta
tcaaactggtttggaaataagcgaatccggtacaagaagaacataggtaaatttcaagag
gaagccaatatttatgctgccaaaacagctgtcactgctaccaatgtgtcagcccatgga
agccaagctaactcgccctcaactcccaactcggctggttcttccagttcttttaacatg
tcaaactctggagatttgttcatgagcgtgcagtcactcaatggggattcttaccaaggg
gcccaggttggagccaacgtgcaatcacaggtggatacccttcgccatgttatcagccag
acaggaggatacagtgatggactcgcagccagtcagatgtacagtccgcagggcatcagt
gctaatggaggttggcaggatgctactaccccttcatcagtgacctcccctacagaaggc
cctggcagtgttcactctgatacctccaactga |