Homo sapiens (human): 1053
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Entry
1053 CDS
T01001
Symbol
CEBPE, C/EBP-epsilon, CRP1, IMD108, SGD1, c/EBP_epsilon
Name
(RefSeq) CCAAT enhancer binding protein epsilon
KO
K10051
CCAAT/enhancer binding protein (C/EBP), epsilon
Organism
hsa
Homo sapiens (human)
Pathway
hsa05202
Transcriptional misregulation in cancer
hsa05221
Acute myeloid leukemia
Network
nt06240
Transcription (cancer)
nt06275
Acute myeloid leukemia
Element
N00113
PML-RARA fusion to transcriptional repression
Disease
H02024
Neutrophil specific granule deficiency
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09160 Human Diseases
09161 Cancer: overview
05202 Transcriptional misregulation in cancer
1053 (CEBPE)
09162 Cancer: specific types
05221 Acute myeloid leukemia
1053 (CEBPE)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
1053 (CEBPE)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Basic leucine zipper (bZIP)
C/EBP-like factors
1053 (CEBPE)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
bZIP_2
bZIP_1
Taxilin
Myc-LZ
UPF0449
Nmad5
Nup54
DUF2605
SBE2
Fib_alpha
Motif
Other DBs
NCBI-GeneID:
1053
NCBI-ProteinID:
NP_001796
OMIM:
600749
HGNC:
1836
Ensembl:
ENSG00000092067
UniProt:
Q15744
Structure
PDB
LinkDB
All DBs
Position
14:complement(23117306..23119255)
Genome browser
AA seq
281 aa
AA seq
DB search
MSHGTYYECEPRGGQQPLEFSGGRAGPGELGDMCEHEASIDLSAYIESGEEQLLSDLFAV
KPAPEARGLKGPGTPAFPHYLPPDPRPFAYPPHTFGPDRKALGPGIYSSPGSYDPRAVAV
KEEPRGPEGSRAASRGSYNPLQYQVAHCGQTAMHLPPTLAAPGQPLRVLKAPLATAAPPC
SPLLKAPSPAGPLHKGKKAVNKDSLEYRLRRERNNIAVRKSRDKAKRRILETQQKVLEYM
AENERLRSRVEQLTQELDTLRNLFRQIPEAANLIKGVGGCS
NT seq
846 nt
NT seq
+upstream
nt +downstream
nt
atgtcccacgggacctactacgagtgtgagccccggggtggccagcagccactcgagttc
tcagggggccgagctgggcccggggagctaggggacatgtgtgagcatgaggcctccatt
gacctctccgcctacatcgagtctggggaagagcagcttctctccgatctctttgccgtg
aagccagcgcctgaggccagaggcctcaagggccccggaacccctgccttcccccactac
ttgccgcctgaccctcggccctttgcctaccctccacataccttcggcccagacaggaag
gcgctggggcctggcatctacagcagcccagggagctacgaccccagggctgtggcggtg
aaggaggagccccgggggccagagggcagccgagctgccagccgaggcagctacaatccc
ctgcagtaccaagtggcacactgtgggcagacagccatgcacctgcccccaactctggca
gcacccggccagcctctgcgcgttctcaaggcccctttggccactgccgcacccccctgc
agtcccctcctgaaggcgccctccccggctggccccttacacaagggcaagaaggcagtg
aacaaagatagccttgagtaccggctgaggcgggagcgcaacaacatcgccgtgcgcaag
agccgagacaaggccaagaggcgcattctggagacgcagcagaaggtgctggagtacatg
gcagagaacgagcgcctccgcagccgcgtggagcagctcacccaggagctagacaccctc
cgcaacctcttccgccagattcctgaggcggccaacctcatcaagggcgtggggggttgc
agctga
Homo sapiens (human): 597
Help
Entry
597 CDS
T01001
Symbol
BCL2A1, ACC-1, ACC-2, ACC1, ACC2, BCL2L5, BFL1, GRS, HBPA1
Name
(RefSeq) BCL2 related protein A1
KO
K02162
hematopoietic Bcl-2-related protein A1
Organism
hsa
Homo sapiens (human)
Pathway
hsa04064
NF-kappa B signaling pathway
hsa04210
Apoptosis
hsa05202
Transcriptional misregulation in cancer
hsa05221
Acute myeloid leukemia
Network
nt06240
Transcription (cancer)
nt06275
Acute myeloid leukemia
Element
N00113
PML-RARA fusion to transcriptional repression
N00123
Amplified REL to transcription
Drug target
Navitoclax (
DG03204
):
D09935
D09936
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04064 NF-kappa B signaling pathway
597 (BCL2A1)
09140 Cellular Processes
09143 Cell growth and death
04210 Apoptosis
597 (BCL2A1)
09160 Human Diseases
09161 Cancer: overview
05202 Transcriptional misregulation in cancer
597 (BCL2A1)
09162 Cancer: specific types
05221 Acute myeloid leukemia
597 (BCL2A1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Bcl-2
CCDC24
DDE_Tnp_1_assoc
Motif
Other DBs
NCBI-GeneID:
597
NCBI-ProteinID:
NP_004040
OMIM:
601056
HGNC:
991
Ensembl:
ENSG00000140379
UniProt:
Q16548
Structure
PDB
LinkDB
All DBs
Position
15:complement(79960892..79971196)
Genome browser
AA seq
175 aa
AA seq
DB search
MTDCEFGYIYRLAQDYLQCVLQIPQPGSGPSKTSRVLQNVAFSVQKEVEKNLKSCLDNVN
VVSVDTARTLFNQVMEKEFEDGIINWGRIVTIFAFEGILIKKLLRQQIAPDVDTYKEISY
FVAEFIMNNTGEWIRQNGGWENGFVKKFEPKSGWMTFLEVTGKICEMLSLLKQYC
NT seq
528 nt
NT seq
+upstream
nt +downstream
nt
atgacagactgtgaatttggatatatttacaggctggctcaggactatctgcagtgcgtc
ctacagataccacaacctggatcaggtccaagcaaaacgtccagagtgctacaaaatgtt
gcgttctcagtccaaaaagaagtggaaaagaatctgaagtcatgcttggacaatgttaat
gttgtgtccgtagacactgccagaacactattcaaccaagtgatggaaaaggagtttgaa
gacggcatcattaactggggaagaattgtaaccatatttgcatttgaaggtattctcatc
aagaaacttctacgacagcaaattgccccggatgtggatacctataaggagatttcatat
tttgttgcggagttcataatgaataacacaggagaatggataaggcaaaacggaggctgg
gaaaatggctttgtaaagaagtttgaacctaaatctggctggatgacttttctagaagtt
acaggaaagatctgtgaaatgctatctctcctgaagcaatactgttga
DBGET
integrated database retrieval system