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MyD88 variants [cytosol]
Stable Identifier
R-HSA-5602754
Type
Set [CandidateSet]
Species
Homo sapiens
Compartment
cytosol
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of Immune System (Homo sapiens)
Diseases associated with the TLR signaling cascade (Homo sapiens)
MyD88 deficiency (TLR2/4) (Homo sapiens)
Defective MyD88 does not oligomerize within the activated TLR2/4 complex (Homo sapiens)
MyD88 variant:TIRAP:BTK:activated TLR2/4 [plasma membrane] (Homo sapiens)
MyD88 variants [cytosol] (Homo sapiens)
MyD88 variants [cytosol] (Homo sapiens)
MyD88 deficiency (TLR5) (Homo sapiens)
Defective MyD88 does not oligomerize within the complex of activated TLR5 (Homo sapiens)
MyD88 variant:TLR5:bacterial flagellin [plasma membrane] (Homo sapiens)
MyD88 variants [cytosol] (Homo sapiens)
MyD88 variants [cytosol] (Homo sapiens)
Participants
members
MyD88 E52del [cytosol]
(Homo sapiens)
MyD88 L93P [cytosol]
(Homo sapiens)
candidates
MyD88 S34Y [cytosol]
(Homo sapiens)
MyD88 E65del [cytosol]
(Homo sapiens)
Participates
as an input of
Defective MyD88 does not oligomerize within the complex of activated TLR5 (Homo sapiens)
Defective MyD88 does not oligomerize within the activated TLR2/4 complex (Homo sapiens)
as a component of
MyD88 variant:TLR5:bacterial flagellin [plasma membrane] (Homo sapiens)
MyD88 variant:TIRAP:BTK:activated TLR2/4 [plasma membrane] (Homo sapiens)
Disease
Name
Identifier
Synonyms
primary immunodeficiency disease
DOID:612
immune deficiency disorder, immunodeficiency syndrome, hypoimmunity
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