Alzheimer's disease and miRNA effects (Homo sapiens)

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C83ATP depletionCalcium overloadp-Mitochondiral dysfunctionsAPP-alpha(Tau-P)nalpha-SecretaseAICDAggr. amyloidOligomeric intracellular ABAmyloid Beta (AB)Neuronp+MicrogliaEndoplasmic reticulum (ER)Modulation of gene expressionNeuronal InjuryCalcium Signaling PathwayIP3APPBP1APPInduction of ApoptosisNOProtein oxidationCell DeathHydrogen peroxideCalciumIronOxidative PhosphorylationCopperApoptosisAPBB1GAPDHADAM10BACE1PSENENPSEN1NCSTNAPH1AIDEMMELPLAPOELRP1FASTNFRSF1AFADDCASP8Cx ICx IICx IIICx IVCx VAPP processingLower energy production?beta-Secretasegamma-SecretaseHSD17B10Fall in mitochondrialsAPP-betaC99membrane potentialIncreased ROSDegredationInactivationBIDCYCSCALM1CHPBADCALM2CALM3CALML3CALML5PPP3CAPPP3CBPPP3CCPPP3R1PPP3R2CHP2ADAM17PSEN2APAF1CASP9CASP3AB AggregationOligomeric ABalpha-synucleinSNCASenileplaqueNACGPCRGRIN1CACNA1CGRIN2AGRIN2BGRIN2CGRIN2DCACNA1DCACNA1FCACNA1SGNAQPLCB1PLCB2PLCB3PLCB4TNFIL1BMAPK1MAPK3CASP12ApoptosisRYR3PSENENATP2A2ATP2A1ATP2A3EIF2AK3ERN1ATF6ITPR1ITPR2ITPR3CalciumCalciumER stressCAPN1CAPN2TP53CDK5R1NOS1CDK5TAUGSK3BCASP3CASP7Paired helical filaments (PHFs)Neurofibrillarytangles (NFTs)p+ABMitochondrial dysfunctionApoptosisDNA damageInflammationLipid peroxidationONOO-


Description

This pathway displays current genes, proteolytic events and other processes associated with the progression of Alzheimer's disease. This pathway was adapted from KEGG on 10/7/2011. Note: mitochondrial associated genes Cx I through Cx V are not currently included, as these correspond to over a hundred distinct factors. See below source URL for more information. Source: KEGG (http://www.genome.jp/kegg/pathway/hsa/hsa05010.html)

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Adapted from KEGG

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Bibliography

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History

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CompareRevisionActionTimeUserComment
128085view01:23, 24 January 2024EweitzFix typo, fix graphically truncated label, standardize case
119468view17:53, 29 June 2021Khanspersadded literature references
119429view23:47, 28 June 2021KhanspersModified title
119428view23:46, 28 June 2021KhanspersModified title
119427view23:43, 28 June 2021Khanspersupdated nonamyloidogenic APP processing
119164view01:14, 19 June 2021Khanspersadded literature references
119163view00:21, 19 June 2021Khanspersadded legend
119162view00:13, 19 June 2021Khanspersadded ptms and updated mutated genes
119161view19:18, 18 June 2021KhanspersUpdated Ab degradation part
119089view05:55, 17 June 2021KhanspersCleaned up the mitochondria part
118932view22:17, 4 June 2021Khansperswork in progress
118931view18:59, 4 June 2021Khanspersreplaced peptide labels with protein nodes
118913view04:38, 4 June 2021KhanspersAdded detail to top left corner
118912view04:15, 4 June 2021Khansperswork in progress
118863view01:01, 3 June 2021KhanspersAdded Wnt signaling
118862view00:29, 3 June 2021Khanspersadded axonal transport defects
118861view00:10, 3 June 2021Khansperswork in progress
118791view23:39, 1 June 2021KhanspersWork in progress
118790view23:12, 1 June 2021Khansperswork in progress
118789view22:28, 1 June 2021KhanspersUpdating with latest information. Work in progress.
118198view05:10, 26 May 2021Khanspersupdate in progress
116396view23:18, 6 May 2021EweitzModified title
115412view11:55, 18 February 2021EgonwMade five more pathways clickable
108233view14:43, 1 December 2019EgonwBetter point to a pathway than a inhibitor metabolite.
108214view11:18, 29 November 2019FehrhartOntology Term : 'DOID:10652' removed !
108091view11:56, 28 November 2019FehrhartOntology Term : 'disease pathway' added !
106706view13:13, 17 September 2019MaintBotHMDB identifier normalization
106521view23:41, 5 September 2019KhanspersModified description
105877view04:50, 16 August 2019KhanspersModified description
105524view05:58, 9 August 2019KhanspersModified description
104977view18:27, 27 June 2019Khanspersremoved KEGG
104976view18:26, 27 June 2019KhanspersModified description
102211view00:06, 11 December 2018Khanspersfixed unconnected interaction
102163view22:07, 4 December 2018Khanspersupdated xrefs for miRNAs
101829view09:35, 12 November 2018EgonwReplaced an old Uniprot data source with the new one.
99069view14:16, 29 October 2018SusanFixed interactions
99043view10:32, 27 October 2018Lovnish.thakurReverted to version '10:25, 27 October 2018' by Lovnish.thakur
99042view10:31, 27 October 2018Lovnish.thakurIncluded RAGE(Receptor for glycosylation end products)interaction with Aβ
99041view10:25, 27 October 2018Lovnish.thakurI have included the Receptor for advanced glycosylation end products(RAGE)in this pathway.Interaction of RAGE with Abeta is also responsible for neuronal damage & inflamation mediated which is mediated by NF-κB & JAK/STAT signaling pathways.
97494view14:02, 23 May 2018Fehrhartfixed connections
97492view13:57, 23 May 2018Fehrhartfixed connections
97491view13:56, 23 May 2018Fehrhartfixed connections
87372view09:56, 22 July 2016MaintBotadded missing graphids
85192view16:05, 23 April 2016EgonwReplaced a mim-conversion with Arrow.
85191view16:01, 23 April 2016EgonwFixed a weird char in a reference.
82906view15:21, 11 November 2015JmeliusCorrect outdated id
79765view02:16, 11 April 2015AlexanderPicoAdded miRNA interactions and refs
79302view19:04, 20 March 2015AlexanderPicoupdated miRNA label
78941view22:47, 16 February 2015KhanspersAdded mir132
78916view21:58, 13 February 2015KhanspersAdded lit ref for mir29

External references

DataNodes

View all...
NameTypeDatabase referenceComment
ADAM10GeneProductENSG00000137845 (Ensembl Human)
ADAM17GeneProductENSG00000151694 (Ensembl Human)
APAF1GeneProductENSG00000120868 (Ensembl Human)
APBB1GeneProductENSG00000166313 (Ensembl Human)
APH1AGeneProductENSG00000117362 (Ensembl Human)
APOEGeneProductENSG00000130203 (Ensembl Human)
APP processingPathway
APPBP1GeneProductENSG00000159593 (Ensembl Human)
APPGeneProductENSG00000142192 (Ensembl Human)
ATF6GeneProductENSG00000118217 (Ensembl Human)
ATP2A1GeneProductENSG00000196296 (Ensembl Human)
ATP2A2GeneProductENSG00000174437 (Ensembl Human)
ATP2A3GeneProductENSG00000074370 (Ensembl Human)
ApoptosisPathwayWP254 (WikiPathways)
BACE1GeneProductENSG00000186318 (Ensembl Human)
BADGeneProductENSG00000002330 (Ensembl Human)
BIDGeneProductENSG00000015475 (Ensembl Human)
CACNA1CGeneProductENSG00000151067 (Ensembl Human)
CACNA1DGeneProductENSG00000157388 (Ensembl Human)
CACNA1FGeneProductENSG00000102001 (Ensembl Human)
CACNA1SGeneProductENSG00000081248 (Ensembl Human)
CALM1GeneProductENSG00000198668 (Ensembl Human)
CALM2GeneProductENSG00000143933 (Ensembl Human)
CALM3GeneProductENSG00000160014 (Ensembl Human)
CALML3GeneProductENSG00000178363 (Ensembl Human)
CALML5GeneProductENSG00000178372 (Ensembl Human)
CAPN1GeneProductENSG00000014216 (Ensembl Human)
CAPN2GeneProductENSG00000162909 (Ensembl Human)
CASP12GeneProductENSG00000204403 (Ensembl Human)
CASP3GeneProductENSG00000164305 (Ensembl Human)
CASP7GeneProductENSG00000165806 (Ensembl Human)
CASP8GeneProductENSG00000064012 (Ensembl Human)
CASP9GeneProductENSG00000132906 (Ensembl Human)
CDK5GeneProductENSG00000164885 (Ensembl Human)
CDK5R1GeneProductENSG00000176749 (Ensembl Human)
CHPGeneProduct11261 (Entrez Gene)
CHP2GeneProduct63928 (Entrez Gene)
CYCSGeneProductENSG00000172115 (Ensembl Human)
Calcium Signaling PathwayPathway
CalciumMetaboliteHMDB00464 (HMDB)
Cell DeathPathway
CopperMetaboliteHMDB00657 (HMDB)
Cx IGeneProduct
Cx IIGeneProduct
Cx IIIGeneProduct
Cx IVGeneProduct
Cx VGeneProduct
DNA damagePathway
EIF2AK3GeneProductENSG00000172071 (Ensembl Human)
ERN1GeneProductENSG00000178607 (Ensembl Human)
FADDGeneProductENSG00000168040 (Ensembl Human)
FASGeneProductENSG00000026103 (Ensembl Human)
GAPDHGeneProductENSG00000111640 (Ensembl Human)
GNAQGeneProductENSG00000156052 (Ensembl Human)
GPCRGeneProduct
GRIN1GeneProductENSG00000176884 (Ensembl Human)
GRIN2AGeneProductENSG00000183454 (Ensembl Human)
GRIN2BGeneProductENSG00000150086 (Ensembl Human)
GRIN2CGeneProductENSG00000161509 (Ensembl Human)
GRIN2DGeneProductENSG00000105464 (Ensembl Human)
GSK3BGeneProductENSG00000082701 (Ensembl Human)
HSD17B10GeneProductENSG00000072506 (Ensembl Human)
Hydrogen peroxideMetaboliteHMDB03125 (HMDB)
IDEGeneProductENSG00000119912 (Ensembl Human)
IL1BGeneProductENSG00000125538 (Ensembl Human)
IP3MetaboliteHMDB01498 (HMDB)
ITPR1GeneProductENSG00000150995 (Ensembl Human)
ITPR2GeneProductENSG00000123104 (Ensembl Human)
ITPR3GeneProductENSG00000096433 (Ensembl Human)
Induction of ApoptosisPathwayWP1896 (WikiPathways)
InflammationPathwayWP453 (WikiPathways)
IronMetaboliteHMDB00692 (HMDB)
LPLGeneProductENSG00000175445 (Ensembl Human)
LRP1GeneProductENSG00000123384 (Ensembl Human)
Lipid peroxidationPathwayWP1878 (WikiPathways)
Lower energy production?Pathway
MAPK1GeneProductENSG00000100030 (Ensembl Human)
MAPK3GeneProductENSG00000102882 (Ensembl Human)
MMEGeneProductENSG00000196549 (Ensembl Human)
Mitochondrial dysfunctionPathway
Modulation of gene expressionPathwayWP1821 (WikiPathways)
NCSTNGeneProductENSG00000162736 (Ensembl Human)
NOMetaboliteHMDB03378 (HMDB)
NOS1GeneProductENSG00000089250 (Ensembl Human)
Neuronal InjuryPathway
ONOO-MetaboliteHMDB02179 (HMDB)
Oxidative PhosphorylationPathwayWP623 (WikiPathways)
PLCB1GeneProductENSG00000182621 (Ensembl Human)
PLCB2GeneProductENSG00000137841 (Ensembl Human)
PLCB3GeneProductENSG00000149782 (Ensembl Human)
PLCB4GeneProductENSG00000101333 (Ensembl Human)
PPP3CAGeneProductENSG00000138814 (Ensembl Human)
PPP3CBGeneProductENSG00000107758 (Ensembl Human)
PPP3CCGeneProductENSG00000120910 (Ensembl Human)
PPP3R1GeneProductENSG00000221823 (Ensembl Human)
PPP3R2GeneProductENSG00000188386 (Ensembl Human)
PSEN1GeneProductENSG00000080815 (Ensembl Human)
PSEN2GeneProductENSG00000143801 (Ensembl Human)
PSENENGeneProductENSG00000205155 (Ensembl Human)
Protein oxidationPathway
RYR3GeneProductENSG00000198838 (Ensembl Human)
SNCAGeneProductENSG00000145335 (Ensembl Human)
TAUGeneProductENSG00000186868 (Ensembl Human)
TNFGeneProductENSG00000232810 (Ensembl Human)
TNFRSF1AGeneProductENSG00000067182 (Ensembl Human)
TP53GeneProductENSG00000141510 (Ensembl Human)

Annotated Interactions

No annotated interactions
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