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MUT mutants [mitochondrial matrix]
Stable Identifier
R-HSA-3323182
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
mitochondrial matrix
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of metabolism (Homo sapiens)
Diseases of mitochondrial beta oxidation (Homo sapiens)
Diseases of propionyl-CoA catabolism (Homo sapiens)
Defective MUT causes MMAM (Homo sapiens)
Defective MUT does not isomerise L-MM-CoA to SUCC-CoA (Homo sapiens)
2xMMAA:mutant MUT:AdoCbl [mitochondrial matrix] (Homo sapiens)
mutant MUT:AdoCbl [mitochondrial matrix] (Homo sapiens)
MUT mutants [mitochondrial matrix] (Homo sapiens)
Participants
members
MUT A378E [mitochondrial matrix]
(Homo sapiens)
MUT G215S [mitochondrial matrix]
(Homo sapiens)
MUT G623R [mitochondrial matrix]
(Homo sapiens)
MUT G703R [mitochondrial matrix]
(Homo sapiens)
MUT N219Y [mitochondrial matrix]
(Homo sapiens)
MUT Q17* [mitochondrial matrix]
(Homo sapiens)
MUT R108C [mitochondrial matrix]
(Homo sapiens)
MUT R93H [mitochondrial matrix]
(Homo sapiens)
MUT W105R [mitochondrial matrix]
(Homo sapiens)
Participates
as a component of
mutant MUT:AdoCbl [mitochondrial matrix] (Homo sapiens)
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