Homo sapiens (human): 8915
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Entry
8915 CDS
T01001
Symbol
BCL10, CARMEN, CIPER, CLAP, IMD37, c-E10, mE10
Name
(RefSeq) BCL10 immune signaling adaptor
KO
K07368
B-cell CLL/lymphoma 10
Organism
hsa
Homo sapiens (human)
Pathway
hsa04064
NF-kappa B signaling pathway
hsa04625
C-type lectin receptor signaling pathway
hsa04660
T cell receptor signaling pathway
hsa04662
B cell receptor signaling pathway
hsa05131
Shigellosis
hsa05152
Tuberculosis
Disease
H00093
Combined immunodeficiency
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04064 NF-kappa B signaling pathway
8915 (BCL10)
09150 Organismal Systems
09151 Immune system
04625 C-type lectin receptor signaling pathway
8915 (BCL10)
04660 T cell receptor signaling pathway
8915 (BCL10)
04662 B cell receptor signaling pathway
8915 (BCL10)
09160 Human Diseases
09171 Infectious disease: bacterial
05131 Shigellosis
8915 (BCL10)
05152 Tuberculosis
8915 (BCL10)
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Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
CARD
TcaA_2nd
Flu_B_NS1
Motif
Other DBs
NCBI-GeneID:
8915
NCBI-ProteinID:
NP_003912
OMIM:
603517
HGNC:
989
Ensembl:
ENSG00000142867
Pharos:
O95999
(Tbio)
UniProt:
O95999
Structure
PDB
PDBj
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All DBs
Position
1:complement(85265776..85276632)
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AA seq
233 aa
AA seq
DB search
MEPTAPSLTEEDLTEVKKDALENLRVYLCEKIIAERHFDHLRAKKILSREDTEEISCRTS
SRKRAGKLLDYLQENPKGLDTLVESIRREKTQNFLIQKITDEVLKLRNIKLEHLKGLKCS
SCEPFPDGATNNLSRSNSDESNFSEKLRASTVMYHPEGESSTTPFFSTNSSLNLPVLEVG
RTENTIFSSTTLPRPGDPGAPPLPPDLQLEEEGTCANSSEMFLPLRSRTVSRQ
NT seq
702 nt
NT seq
+upstream
nt +downstream
nt
atggagcccaccgcaccgtccctcaccgaggaggacctcactgaagtgaagaaggacgcc
ttagaaaatttacgtgtatacctgtgtgagaaaatcatagctgagagacattttgatcat
ctacgtgcaaaaaaaatactcagtagagaagacactgaagaaatttcttgtcgaacatca
agtagaaaaagggctggaaaattgttagactacttacaggaaaacccaaaaggtctggac
acccttgttgaatctattcggcgagaaaaaacacagaacttcctgatacagaagattaca
gatgaagtgctgaaacttagaaatataaaactagaacatctgaaaggactaaaatgtagc
agttgtgaaccttttccagatggagccacgaacaacctctccagatcaaattcagatgag
agtaatttctctgaaaaactgagggcatccactgtcatgtaccatccagaaggagaatcc
agcacgacgccctttttttctactaattcttctctgaatttgcctgttctagaagtaggc
agaactgaaaataccatcttctcttcaactacacttcccagacctggggacccaggggct
cctcctttgccaccagatctacagttagaagaagaaggaacttgtgcaaactctagtgag
atgtttcttcccttaagatcacgtactgtttcacgacaatga
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