Entity Detail — Knowledge Graph Node
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.
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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| Name | CRY |
| Key Genes/Proteins | ALZHEIMER, AMPK, AND, ARNT, BMAL1, CAMK2A |
| Related Diseases | Als, ALS, Alzheimer, Cancer, Cardiovascular |
Knowledge base pages for this entity
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| Target | Relation | Type | Str |
|---|---|---|---|
| METABOLIC HEALTH | regulates | entity | 0.95 |
| circadian rhythm | drives | process | 0.95 |
| Circadian Gene Expression | involved_in | process | 0.90 |
| CLOCK-BMAL1 | inhibits | protein | 0.90 |
| Circadian Rhythm Regulation | regulates | process | 0.90 |
| Glioblastoma Growth | regulates | phenotype | 0.90 |
| Circadian Rhythms | involved_in | process | 0.90 |
| Cellular Metabolism | regulates | process | 0.90 |
| LIPID METABOLISM | regulates | entity | 0.85 |
| Insomnia | associated_with | disease | 0.80 |
| Metabolism | regulates | process | 0.80 |
| circadian rhythm | participates_in | process | 0.80 |
| Metabolic Syndrome | interacts_with | disease | 0.65 |
| Cancer | interacts_with | disease | 0.65 |
| ALS | regulates | disease | 0.65 |
| ALS | activates | disease | 0.65 |
| circadian regulation | participates_in | pathway | 0.65 |
| Als | activates | disease | 0.65 |
| Tumor | activates | disease | 0.65 |
| Ms | activates | disease | 0.65 |
| Neuroinflammation | regulates | disease | 0.65 |
| Alzheimer | regulates | disease | 0.65 |
| Parkinson | regulates | disease | 0.65 |
| Cancer | associated_with | disease | 0.65 |
| Cardiovascular | associated_with | disease | 0.65 |
| Diabetes | associated_with | disease | 0.65 |
| Metabolic Syndrome | associated_with | disease | 0.65 |
| Obesity | associated_with | disease | 0.65 |
| Depression | expressed_in | disease | 0.65 |
| Obesity | regulates | disease | 0.65 |
| Ms | regulates | disease | 0.65 |
| Cancer | expressed_in | disease | 0.65 |
| Cardiovascular | expressed_in | disease | 0.65 |
| Metabolic Syndrome | expressed_in | disease | 0.65 |
| Obesity | expressed_in | disease | 0.65 |
| Ms | expressed_in | disease | 0.65 |
| Diabetes | expressed_in | disease | 0.65 |
| Diabetes | regulates | disease | 0.65 |
| Inflammation | regulates | disease | 0.65 |
| Cancer | activates | disease | 0.65 |
| Als | regulates | disease | 0.65 |
| Glioblastoma | activates | disease | 0.65 |
| GENES | inhibits | gene | 0.60 |
| BMAL1 | associated_with | gene | 0.60 |
| CLOCK | associated_with | gene | 0.60 |
| Oxidative Stress | regulates | pathway | 0.60 |
| Lipid Metabolism | regulates | pathway | 0.60 |
| Circadian Rhythm | regulates | pathway | 0.60 |
| Sleep-Wake | regulates | pathway | 0.60 |
| BMAL1 | expressed_in | gene | 0.60 |
| Source | Relation | Type | Str |
|---|---|---|---|
| PER | interacts_with | gene | 0.80 |
| BMAL1 | associated_with | gene | 0.60 |
| GENES | associated_with | gene | 0.60 |
| GENES | expressed_in | gene | 0.60 |
| GENES | activates | gene | 0.60 |
| CLOCK | associated_with | gene | 0.60 |
| ARNT | expressed_in | gene | 0.60 |
| BMAL1 | expressed_in | gene | 0.60 |
| CLOCK | expressed_in | gene | 0.60 |
| BMAL1 | activates | gene | 0.60 |
| CLOCK | activates | gene | 0.60 |
| ALZHEIMER | regulates | gene | 0.60 |
| NEURODEGENERATIVE DISORDERS | regulates | gene | 0.60 |
| NEURODEGENERATIVE DISEASES | regulates | gene | 0.60 |
| PER | associated_with | gene | 0.60 |
| PARKINSON | regulates | gene | 0.60 |
| PER | expressed_in | gene | 0.60 |
| BMAL1 | interacts_with | gene | 0.60 |
| CLOCK | interacts_with | gene | 0.60 |
| CRY1 | inhibits | gene | 0.60 |
| CANCER | interacts_with | gene | 0.60 |
| DNA | interacts_with | gene | 0.60 |
| REST | interacts_with | gene | 0.60 |
| GENES | regulates | gene | 0.60 |
| OXIDATIVE STRESS | regulates | gene | 0.60 |
| NEUROINFLAMMATION | regulates | gene | 0.60 |
| PER | inhibits | gene | 0.60 |
| CAMK2A | expressed_in | gene | 0.60 |
| GLIOBLASTOMA | activates | gene | 0.60 |
| GBM | activates | gene | 0.60 |
| PER | activates | gene | 0.60 |
| CIRCADIAN OUTPUT GENES | expressed_in | gene | 0.60 |
| CANCER | expressed_in | gene | 0.60 |
| CLOCK GENE | expressed_in | gene | 0.60 |
| ARNT | regulates | gene | 0.60 |
| BMAL1 | regulates | gene | 0.60 |
| CLOCK | regulates | gene | 0.60 |
| AND | activates | gene | 0.60 |
| CANCER | activates | gene | 0.60 |
| CLOCK GENES | activates | gene | 0.60 |
| AMPK | causes | gene | 0.60 |
Hypotheses where this entity is a therapeutic target
| Hypothesis | Score | Disease | Analysis |
|---|---|---|---|
| SFPQ Paralog Displacement Triggers Cryptic Polyadenylation a | 0.864 | ALS | - |
| STMN2 Cryptic Exon Inclusion is the Earliest Loss-of-Functio | 0.721 | 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 |
Scientific analyses that reference this entity
No analyses mention this entity
Experimental studies targeting or related to this entity
| Experiment | Type | Disease | Score | Feasibility | Model | Status | Est. 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 |
Scientific publications cited in analyses involving this entity
| Title & PMID | Authors | Journal | Year | Citations |
|---|---|---|---|---|
| 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 |
Multi-agent debates referencing this entity
No debates reference this entity
Hypotheses and analyses mentioning CRY in their description or question text
No additional research found