Entry |
|
Name |
Mutation-caused aberrant Abeta to electron transfer in Complex IV
|
Definition |
APP* -> Abeta -| CxIV -> H2O |
Expanded |
351v1 -> (C16515,C16514) -| (4514+4512+4513+(1327,84701)+9377+1329+(1337,1339)+(1340,125965)+1345+(1346,1347,9167)+1349+1350+(1351,341947)) -> C00001 |
Class |
|
Type |
Variant
|
Pathway |
|
Disease |
|
Gene |
351 | APP; amyloid beta precursor protein |
4514 | COX3; cytochrome c oxidase III |
4512 | COX1; cytochrome c oxidase subunit I |
4513 | COX2; cytochrome c oxidase subunit II |
1327 | COX4I1; cytochrome c oxidase subunit 4I1 |
84701 | COX4I2; cytochrome c oxidase subunit 4I2 |
9377 | COX5A; cytochrome c oxidase subunit 5A |
1329 | COX5B; cytochrome c oxidase subunit 5B |
1337 | COX6A1; cytochrome c oxidase subunit 6A1 |
1339 | COX6A2; cytochrome c oxidase subunit 6A2 |
1340 | COX6B1; cytochrome c oxidase subunit 6B1 |
125965 | COX6B2; cytochrome c oxidase subunit 6B2 |
1345 | COX6C; cytochrome c oxidase subunit 6C |
1346 | COX7A1; cytochrome c oxidase subunit 7A1 |
1347 | COX7A2; cytochrome c oxidase subunit 7A2 |
9167 | COX7A2L; cytochrome c oxidase subunit 7A2 like |
1349 | COX7B; cytochrome c oxidase subunit 7B |
1350 | COX7C; cytochrome c oxidase subunit 7C |
1351 | COX8A; cytochrome c oxidase subunit 8A |
341947 | COX8C; cytochrome c oxidase subunit 8C |
|
Variant |
351v1 (APP*) APP mutation
|
Metabolite |
C16515 | Beta-amyloid protein 42 |
C16514 | Beta-amyloid protein 40 |
|
Reference |
|
Authors |
Hauptmann S, Keil U, Scherping I, Bonert A, Eckert A, Muller WE |
Title |
Mitochondrial dysfunction in sporadic and genetic Alzheimer's disease. |
Journal |
|
Reference |
|
Authors |
Golpich M, Amini E, Mohamed Z, Azman Ali R, Mohamed Ibrahim N, Ahmadiani A |
Title |
Mitochondrial Dysfunction and Biogenesis in Neurodegenerative diseases: Pathogenesis and Treatment. |
Journal |
|
Reference |
|
Authors |
Lin MT, Beal MF |
Title |
Mitochondrial dysfunction and oxidative stress in neurodegenerative diseases. |
Journal |
|
Reference |
|
Authors |
Rodolfo C, Ciccosanti F, Giacomo GD, Piacentini M, Fimia GM |
Title |
Proteomic analysis of mitochondrial dysfunction in neurodegenerative diseases. |
Journal |
|
LinkDB |
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