Homo sapiens (human): 1051
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Entry
1051 CDS
T01001
Symbol
CEBPB, C/EBP-beta, IL6DBP, NF-IL6, TCF5
Name
(RefSeq) CCAAT enhancer binding protein beta
KO
K10048
CCAAT/enhancer binding protein (C/EBP), beta
Organism
hsa
Homo sapiens (human)
Pathway
hsa04148
Efferocytosis
hsa04657
IL-17 signaling pathway
hsa04668
TNF signaling pathway
hsa05152
Tuberculosis
hsa05202
Transcriptional misregulation in cancer
Network
nt06240
Transcription (cancer)
nt06535
Efferocytosis
Element
N00139
FUS-DDIT3 fusion to CEBPB-mediated transcription
N01751
Macrophage EPO signaling
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04668 TNF signaling pathway
1051 (CEBPB)
09140 Cellular Processes
09141 Transport and catabolism
04148 Efferocytosis
1051 (CEBPB)
09150 Organismal Systems
09151 Immune system
04657 IL-17 signaling pathway
1051 (CEBPB)
09160 Human Diseases
09161 Cancer: overview
05202 Transcriptional misregulation in cancer
1051 (CEBPB)
09171 Infectious disease: bacterial
05152 Tuberculosis
1051 (CEBPB)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
1051 (CEBPB)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Basic leucine zipper (bZIP)
C/EBP-like factors
1051 (CEBPB)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
bZIP_2
bZIP_1
ATG16
Taxilin
DUF3450
CCD48
Uds1
DivIC
UPF0242
Nup54
bZIP_Maf
Motif
Other DBs
NCBI-GeneID:
1051
NCBI-ProteinID:
NP_005185
OMIM:
189965
HGNC:
1834
Ensembl:
ENSG00000172216
Pharos:
P17676
(Tbio)
UniProt:
P17676
Structure
PDB
LinkDB
All DBs
Position
20:50190583..50192690
Genome browser
AA seq
345 aa
AA seq
DB search
MQRLVAWDPACLPLPPPPPAFKSMEVANFYYEADCLAAAYGGKAAPAAPPAARPGPRPPA
GELGSIGDHERAIDFSPYLEPLGAPQAPAPATATDTFEAAPPAPAPAPASSGQHHDFLSD
LFSDDYGGKNCKKPAEYGYVSLGRLGAAKGALHPGCFAPLHPPPPPPPPPAELKAEPGFE
PADCKRKEEAGAPGGGAGMAAGFPYALRAYLGYQAVPSGSSGSLSTSSSSSPPGTPSPAD
AKAPPTACYAGAAPAPSQVKSKAKKTVDKHSDEYKIRRERNNIAVRKSRDKAKMRNLETQ
HKVLELTAENERLQKKVEQLSRELSTLRNLFKQLPEPLLASSGHC
NT seq
1038 nt
NT seq
+upstream
nt +downstream
nt
atgcaacgcctggtggcctgggacccagcatgtctccccctgccgccgccgccgcctgcc
tttaaatccatggaagtggccaacttctactacgaggcggactgcttggctgctgcgtac
ggcggcaaggcggcccccgcggcgccccccgcggccagacccgggccgcgcccccccgcc
ggcgagctgggcagcatcggcgaccacgagcgcgccatcgacttcagcccgtacctggag
ccgctgggcgcgccgcaggccccggcgcccgccacggccacggacaccttcgaggcggct
ccgcccgcgcccgcccccgcgcccgcctcctccgggcagcaccacgacttcctctccgac
ctcttctccgacgactacgggggcaagaactgcaagaagccggccgagtacggctacgtg
agcctggggcgcctgggggccgccaagggcgcgctgcaccccggctgcttcgcgcccctg
cacccaccgcccccgccgccgccgccgcccgccgagctcaaggcggagccgggcttcgag
cccgcggactgcaagcggaaggaggaggccggggcgccgggcggcggcgcaggcatggcg
gcgggcttcccgtacgcgctgcgcgcttacctcggctaccaggcggtgccgagcggcagc
agcgggagcctctccacgtcctcctcgtccagcccgcccggcacgccgagccccgctgac
gccaaggcgcccccgaccgcctgctacgcgggggccgcgccggcgccctcgcaggtcaag
agcaaggccaagaagaccgtggacaagcacagcgacgagtacaagatccggcgcgagcgc
aacaacatcgccgtgcgcaagagccgcgacaaggccaagatgcgcaacctggagacgcag
cacaaggtcctggagctcacggccgagaacgagcggctgcagaagaaggtggagcagctg
tcgcgcgagctcagcaccctgcggaacttgttcaagcagctgcccgagcccctgctcgcc
tcctccggccactgctag
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