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TPR mutants [nucleoplasm]
Stable Identifier
R-HSA-5661416
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
nucleoplasm
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Disorders of transmembrane transporters (Homo sapiens)
SLC transporter disorders (Homo sapiens)
Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC) (Homo sapiens)
Defective NPC does not transport GCK1:GKRP from cytosol to nucleoplasm (Homo sapiens)
Defective NPC [nuclear envelope] (Homo sapiens)
TPR mutants [nucleoplasm] (Homo sapiens)
Participants
members
TPR L458P [nucleoplasm]
(Homo sapiens)
TPR M489P [nucleoplasm]
(Homo sapiens)
Participates
as a component of
Defective NPC [nuclear envelope] (Homo sapiens)
Disease
Name
Identifier
Synonyms
papillary carcinoma
DOID:3113
Papillary carcinoma (morphologic abnormality), Papillary carcinoma, Papillary carcinoma NOS (morphologic abnormality)
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