Entry
Name
Mutation-caused aberrant PSEN1 to mGluR5-Ca2+ -apoptotic pathway
Definition
PSEN1* -> ITPR -> Ca2+ -- MCU -> Ca2+(mito) -- MPTP -> CYCS
Expanded
5663v1 -> (3708,3709,3710) -> C00076 -- 90550 -> C00076 -- (7416,7417,7419,291,292,293,83447) -> 54205
Class
Type
Variant
Pathway
Disease
Gene
3708 ITPR1; inositol 1,4,5-trisphosphate receptor type 1
3709 ITPR2; inositol 1,4,5-trisphosphate receptor type 2
3710 ITPR3; inositol 1,4,5-trisphosphate receptor type 3
90550 MCU; mitochondrial calcium uniporter
7416 VDAC1; voltage dependent anion channel 1
7417 VDAC2; voltage dependent anion channel 2
7419 VDAC3; voltage dependent anion channel 3
291 SLC25A4; solute carrier family 25 member 4
292 SLC25A5; solute carrier family 25 member 5
293 SLC25A6; solute carrier family 25 member 6
83447 SLC25A31; solute carrier family 25 member 31
54205 CYCS; cytochrome c, somatic
Variant
5663v1 (PSEN1*) PSEN1 mutation
Metabolite
Reference
Authors
Toglia P, Ullah G
Title
The gain-of-function enhancement of IP3-receptor channel gating by familial Alzheimer's disease-linked presenilin mutants increases the open probability of mitochondrial permeability transition pore.
Journal
Reference
Authors
Honarnejad K, Herms J
Title
Presenilins: role in calcium homeostasis.
Journal
Reference
Authors
Mattson MP
Title
ER calcium and Alzheimer's disease: in a state of flux.
Journal
Reference
Authors
Cowburn RF, Popescu BO, Ankarcrona M, Dehvari N, Cedazo-Minguez A
Title
Presenilin-mediated signal transduction.
Journal
LinkDB
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