concept

CRY

Entity Detail — Knowledge Graph Node

Understanding Entity Pages

This page aggregates everything SciDEX knows about CRY: its mechanistic relationships (Knowledge Graph edges), hypotheses targeting it, analyses mentioning it, and supporting scientific papers. The interactive graph below shows its immediate neighbors. All content is AI-synthesized from peer-reviewed literature.

126Connections
5Hypotheses
0Analyses
50Outgoing
41Incoming
10Experiments
0Debates

Summary

CRY is a concept in neurodegeneration research. Key relationships include: regulates, expressed in, activates. Associated with ALS, Als, Alzheimer. Connected to 84 entities in the SciDEX knowledge graph.

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💡 Concept Info
NameCRY
Key Genes/ProteinsALZHEIMER, AMPK, AND, ARNT, BMAL1, CAMK2A
Related DiseasesAls, ALS, Alzheimer, Cancer, Cardiovascular

Wiki Pages (6)

Knowledge base pages for this entity

CRYAB Gene

gene · 2300 words

αB-Crystallin (CRYAB)

protein · 2119 words

CRY1 Gene

gene · 879 words

CRY2 Gene

gene · 716 words

CRY1 Protein

protein · 664 words

Pathway Diagram

graph TD
    CRY["CRY"]
    CRY -->|"inhibits"| CLOCK_BMAL1["CLOCK-BMAL1"]
    CRY -->|"involved_in"| Circadian_Rhythms["Circadian Rhythms"]
    CRY -->|"regulates"| Cellular_Metabolism["Cellular Metabolism"]
    CRY -->|"regulates"| Inflammation["Inflammation"]
    CRY -->|"regulates"| Als["Als"]
    CRY -->|"regulates"| Neuroinflammation["Neuroinflammation"]
    CRY -->|"regulates"| Alzheimer["Alzheimer"]
    CRY -->|"regulates"| Parkinson["Parkinson"]
    CRY -->|"regulates"| Obesity["Obesity"]
    CRY -->|"regulates"| Ms["Ms"]
    PER["PER"] -->|"interacts"| CRY
    GENES["GENES"] -->|"expressed in"| CRY
    ARNT["ARNT"] -->|"expressed in"| CRY
    BMAL1["BMAL1"] -->|"expressed in"| CRY
    CLOCK["CLOCK"] -->|"expressed in"| CRY
    CAMK2A["CAMK2A"] -->|"expressed in"| CRY

Outgoing (85)

TargetRelationTypeStr
METABOLIC HEALTHregulatesentity0.95
circadian rhythmdrivesprocess0.95
CLOCK-BMAL1inhibitsprotein0.90
Circadian Rhythmsinvolved_inprocess0.90
Cellular Metabolismregulatesprocess0.90

Incoming (41)

SourceRelationTypeStr
PERinteracts_withgene0.80
GENESexpressed_ingene0.60
GENESactivatesgene0.60
ALZHEIMERregulatesgene0.60
NEURODEGENERATIVE DISORDERSregulatesgene0.60

Targeting Hypotheses (5)

Hypotheses where this entity is a therapeutic target

HypothesisScoreDiseaseAnalysis
SFPQ Paralog Displacement Triggers Cryptic Polyadenylation a 0.850 ALS -
STMN2 Cryptic Exon Inclusion is the Earliest Loss-of-Functio 0.702 ALS Causal Sequence of TDP-43 Nuclear Cleara
H2: H3K9me3 Heterochromatin Collapse Enables Cryptic Transcr 0.610 neurodegeneration Investigate mechanisms of epigenetic rep
TDP-43 Cryptic Exon–Targeted ASOs to Restore Hippocampal Gam 0.577 neurodegeneration RNA binding protein dysregulation across
Cryptic Exon Silencing Restoration 0.531 neurodegeneration RNA binding protein dysregulation across

Mentioning Analyses (0)

Scientific analyses that reference this entity

No analyses mention this entity

Experiments (10)

Experimental studies targeting or related to this entity

ExperimentTypeDiseaseScoreFeasibilityModelStatusEst. Cost
TDP-43 mutant mouse model cGAS/STING pathway analysis validation amyotrophic lateral sclerosis 0.900 0.00 TDP-43 mutant mice proposed N/A
TDP-43 mitochondrial invasion and DNA release via mPTP exploratory amyotrophic lateral sclerosis 0.900 0.00 cultured cells proposed N/A
TDP-43 mitochondrial invasion and mtDNA release in iPSC motor neurons exploratory Amyotrophic Lateral Sclerosis 0.900 0.00 iPSC-derived motor neurons proposed N/A
cGAS/STING pathway validation in TDP-43 mutant mice validation Amyotrophic Lateral Sclerosis 0.850 0.00 TDP-43 mutant mice proposed N/A
cGAMP biomarker analysis in ALS patient spinal cord samples exploratory Amyotrophic Lateral Sclerosis 0.800 0.00 Human ALS patient spinal cord proposed N/A
TDP-43 pathology prevalence and distribution in AD cases exploratory Alzheimer's disease 0.800 0.00 human postmortem brain tissue proposed N/A
Cognitive impact of TDP-43 pathology in AD patients clinical Alzheimer's disease 0.700 0.00 human patients completed N/A
s:** - Temporal analysis showing mitochondrial defects precede other p falsification Neurodegeneration 0.400 0.50 cell_line proposed $80,000
Proposed experiment from debate on TDP-43 undergoes liquid-liquid phas falsification Neurodegeneration 0.400 0.50 cell_line proposed $80,000
s:** - Single-cell RNA-seq to measure editing efficiency across differ falsification ALS 0.400 0.50 cell_line proposed $150,000

Related Papers (20)

Scientific publications cited in analyses involving this entity

Title & PMIDAuthorsJournalYearCitations
Targets and Gene Therapy of ALS (Part 1). [PMID:40362304] Shiryaeva O, Tolochko C, Alekseeva T, Dy Int J Mol Sci 2025 1
The genetics of amyotrophic lateral sclerosis. [PMID:38967083] Nijs M, Van Damme P Curr Opin Neurol 2024 1
TDP-43 regulates LC3ylation in neural tissue through ATG4B cryptic splicing inhi [PMID:39305312] Torres P, Rico-Rios S, Ceron-Codorniu M, Acta Neuropathol 2024 1
TDP-43 loss and ALS-risk SNPs drive mis-splicing and depletion of UNC13A. [PMID:35197628] Brown AL, Wilkins OG, Keuss MJ, Kargbo-H Nature 2022 1
Therapeutic reduction of ataxin-2 extends lifespan and reduces pathology in TDP- [PMID:28405022] Becker LA, Huang B, Bieri G, Ma R, Knowl Nature 2017 1
Selective Silencing of TDP-43 P. G376D Mutation Reverses Key Amyotrophic Lateral [PMID:41897327] Romano R, Ruotolo G, Perrone F, Tomasell Biomolecules 2026 0
ALS-related proteinopathies: From TDP-43 to mitochondrial proteinopathies. [PMID:41570741] Genin EC, Paquis-Flucklinger V Current opinion in neurobiolog 2026 0
Chemical and Molecular Strategies in Restoring Autophagic Flux in TDP-43 Protein [PMID:41900026] Jamerlan A, Hulme J Molecules (Basel, Switzerland) 2026 0
Axonal transport impairment as an upstream mechanism in amyotrophic lateral scle [PMID:41890591] Gabbay U Frontiers in neuroscience 2026 0
Role of Alpha-Synuclein in Frontotemporal Dementia: Narrative Review. [PMID:41827903] Bougea A Cells 2026 0
Versatile CRISPR-Cas Tools for Gene Regulation in Zebrafish via an Enhanced Q Bi [PMID:41671402] ["Shi M", "Ge W", "Li C", "Liu B", "Deng Advanced science (Weinheim, Ba 2026 0
Splicing the narrative: alternative TARDBP splicing and its relation to neurodeg [PMID:41837283] Miller MR, Dykstra M, Barmada S The Journal of clinical invest 2026 0
Multi-modal dissection of cell-type specific TDP-43 pathology in the motor corte [PMID:41803120] Ruf WP, Kühlwein JK, Meier L, Brockmann Nature communications 2026 0
A neurotoxic cryptic peptide arising from TDP-43-dependent cryptic splicing of P [PMID:41720774] ["Yang M", "Wang Q", "Yan R", "Kang D", Nature communications 2026 0
The Genetics of TDP-43 Type C Neurodegeneration: A Whole-Genome Sequencing Study [PMID:41883703] Nassan M, Ayala I, Sloan J, Bonfitto A, Neurology. Genetics 2026 0
Excitotoxicity in amyotrophic lateral sclerosis: a key pathogenic mechanism. [PMID:41890274] Silva-Hucha S, Hernández RG, Baena-López Brain communications 2026 0
PPAR-Delta Agonist Therapies Did Not Rescue Hallmark Disease Phenotypes in Two S [PMID:41751955] ["Luong D", "Niu C", "Kim E", "Tanji N", International journal of molec 2026 0
Transcriptomic signature of frontotemporal lobar degeneration with TDP-43 type C [PMID:41789476] ["Rajicic A", "Mol M", "Melhem S", "Kisi Brain : a journal of neurology 2026 0
Antisense oligonucleotide targeting TARDBP-EGFR splicing axis inhibits progressi [PMID:41540015] Ni N, Wang M, Yuan Z, Zhang L, Cai J, Du International journal of oral 2026 0
TDP-43 impairs glycolysis by sequestering hexokinase 1 in amyotrophic lateral sc [PMID:41838122] Barone C, Wang R, Cooke S, Ng HP, Ferrei Acta neuropathologica 2026 0

Debates (0)

Multi-agent debates referencing this entity

No debates reference this entity

Related Research

Hypotheses and analyses mentioning CRY in their description or question text

No additional research found