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CYP17A1 mutants [endoplasmic reticulum membrane]
Stable Identifier
R-HSA-5601806
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 CYP17A1 causes AH5 (Homo sapiens)
Defective CYP17A1 does not 17-hydroxylate P4 (Homo sapiens)
CYP17A1 mutants [endoplasmic reticulum membrane] (Homo sapiens)
Defective CYP17A1 does not 17-hydroxylate PREG (Homo sapiens)
CYP17A1 mutants [endoplasmic reticulum membrane] (Homo sapiens)
Defective CYP17A1 does not cleave 17aHPROG (Homo sapiens)
CYP17A1 mutants [endoplasmic reticulum membrane] (Homo sapiens)
Participants
members
CYP17A1 R347H [endoplasmic reticulum membrane]
(Homo sapiens)
CYP17A1 R358Q [endoplasmic reticulum membrane]
(Homo sapiens)
CYP17A1 R362C [endoplasmic reticulum membrane]
(Homo sapiens)
CYP17A1 R96Q [endoplasmic reticulum membrane]
(Homo sapiens)
CYP17A1 R96W [endoplasmic reticulum membrane]
(Homo sapiens)
CYP17A1 S106P [endoplasmic reticulum membrane]
(Homo sapiens)
CYP17A1 W17* [endoplasmic reticulum membrane]
(Homo sapiens)
CYP17A1 W406R [endoplasmic reticulum membrane]
(Homo sapiens)
Disease
Name
Identifier
Synonyms
adrenal gland disease
DOID:9553
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