KEGG    Network variation - RLR signaling
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ENTRYnt06519
NameRLR signaling
CategoryPathway view; Immune system
Pathwayhsa04622 RIG-I-like receptor signaling pathway
DiseaseH00290 Aicardi-Goutieres syndrome
H01571 Singleton-Merten syndrome
Display drug-target relation   disease type
N00469      RNA→RIGI→MAVS→TRAF3→(TANK+NAP1+SINTBAD..→(TBK1+IKBKE)→(IRF7,IRF3)⇒(IFNA,IFNB1)
    SGMRT2     RIGI*↗
    IIAE5         TRAF3*
N00728    IAV   NS1⊣RIGI
N00565    HSV   US11⊣(RIGI,MDA5)
N00685    MV   V⊣MDA5→MAVS
N00271    HCV     (NS3,NS4A)⊣MAVS
N00268    HBV     X⊣MAVS
N00732    IAV     (PB1F2,PB2)⊣MAVS
N00566    HSV       UL36USP⊣TRAF3
N00567    HSV           ICP34.5⊣(TBK1+IKBKE)
N00734    IAV           (PB1F2+CALCOCO2)⊣(TBK1+IKBKE)
N01310    SARS-CoV-2           nsp13⊣TBK1
N01320    SARS-CoV-2           nsp3⊣ISG15=IRF3
N00686    MV             N→IRF3⇒IFNB1
N00568    HSV             US3⊣IRF3
N00470    EBV             BGLF4⊣IRF3
N00687    MV             (V,C)⊣IRF3
N01319    SARS-CoV-2             (nsp6,ORF6)⊣IRF3
 
N01308      RNA→(MDA5,ZNFX1)→MAVS→TRAF3→(TANK+NAP1+SINTBAD..→(TBK1+IKBKE)→(IRF7,IRF3)⇒(IFNA,IFNB1)
    AGS7/SGMRT1     MDA5*↗
    IMD95     MDA5*
    IMD91     ZNFX1*
N01309    SARS-CoV-2 nsp3⊣ISG15=MDA5
 
N00688      RNA→RIGI→MAVS→IKK→NFKBIA→NFKB⇒(IFNA,IFNB1)
N00689    MV           (V,P,C)⊣NFKB
N00730    IAV           NS1⊣NFKB
 
N01564      RNF125⊣(RIGI,MDA5)
    Tenorio syndrome   RNF125*
 
N01565    ADAR⊣RNA
    AGS6/DSH ADAR*

Disease nameDisease category
SGMRT2H01571Singleton-Merten syndromeCongenital malformation
IIAE5H02536Infection-induced acute encephalopathyNervous system disease
IAVH00398InfluenzaViral infectious disease
HSVH00365Herpes simplex virus infectionViral infectious disease
MVH00394MeaslesViral infectious disease
HCVH00048Hepatocellular carcinomaCancer
HBVH00048Hepatocellular carcinomaCancer
SARS-CoV-2H02398COVID-19Viral infectious disease
EBVH00008Burkitt lymphomaCancer
H00007Hodgkin lymphomaCancer
H00054Nasopharyngeal cancerCancer
AGS7/SGMRT1H00290Aicardi-Goutieres syndromeImmune system disease
H01571Singleton-Merten syndromeCongenital malformation
IMD95H02525Disorders of innate immunityImmune system disease
IMD91H02525Disorders of innate immunityImmune system disease
Tenorio syndromeH01806Tenorio syndromeCongenital malformation
AGS6/DSHH00290Aicardi-Goutieres syndromeImmune system disease
H00880Dyschromatosis symmetrica hereditariaSkin disease