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CYP26C1 mutants [endoplasmic reticulum membrane]
Stable Identifier
R-HSA-5602169
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
endoplasmic reticulum membrane
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of metabolism (Homo sapiens)
Metabolic disorders of biological oxidation enzymes (Homo sapiens)
Defective CYP26C1 causes FFDD4 (Homo sapiens)
Defective CYP26C1 does not 4-hydroxylate 9cRA (Homo sapiens)
CYP26C1 mutants [endoplasmic reticulum membrane] (Homo sapiens)
Participants
members
CYP26C1 Q284Hfs*129 [endoplasmic reticulum membrane]
(Homo sapiens)
CYP26C1 R478H [endoplasmic reticulum membrane]
(Homo sapiens)
Disease
Name
Identifier
Synonyms
skin benign neoplasm
DOID:3165
neoplasm of skin (disorder), tumor of the skin, neoplasm of skin by site, skin neoplasm
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