gene

COASY

Entity Detail — Knowledge Graph Node

Understanding Entity Pages

This page aggregates everything SciDEX knows about COASY: 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.

14Connections
0Hypotheses
0Analyses
12Outgoing
2Incoming

Summary

COASY encodes Coenzyme A synthetase, a bifunctional enzyme in CoA biosynthesis. COASY mutations cause COASY Protein-Associated Neurodegeneration (CPAN), a form of NBIA with brain iron accumulation, dystonia, and cognitive decline.

View on Wiki →

🧬 Gene Info
Gene SymbolCOASY
Full NameCoenzyme A Synthetase
Chromosome17q21.2
Protein TypeEnzyme
Functionencodes a bifunctional enzyme that plays a critical role in the coenzyme A (CoA) biosynthetic pathway.
Molecular Weight80 kDa
Amino Acids724 aa
Exons15
UniProt IDQ9P2R3
NCBI Gene ID80317
Ensembl IDENSG00000167468
OMIM609856
GeneCardsCOASY
Human Protein AtlasCOASY
ATP-binding motifRequired for both kinase and adenylyltransferase activities
Associated DiseasesDystonia, Ms, Neurodegeneration, Parkinson
KG Connections14 knowledge graph edges
DatabasesGeneCardsHPASTRING
🔮 Predicted Structure: COASY — AlphaFold Q9P2R3 Click to expand

AI-predicted structure from AlphaFold | Powered by Mol*

Wiki Pages (18)

Knowledge base pages for this entity

Canonical Page

COASY Gene

gene · 1155 words

Infantile Neuroaxonal Dystrophy (INAD)

disease · 3473 words

PKAN Mechanistic Pathway

mechanism · 3040 words

C19orf12 Gene - Chromosome 19 Open Reading Frame 12

gene · 2375 words

Pantothenate Kinase-Associated Neurodegeneration (PKAN)

disease · 2291 words

metal-dyshomeostasis

mechanism · 2282 words

Pathway Diagram

graph TD
    COASY["<b>COASY</b>"]
    Neurodegeneration{"Neurodegeneration"}
    COASY -->|"associated with"| Neurodegeneration
    Ms{"Ms"}
    COASY -->|"associated with"| Ms
    Parkinson{"Parkinson"}
    COASY -->|"associated with"| Parkinson
    Dystonia{"Dystonia"}
    COASY -->|"associated with"| Dystonia
    DCAF17["DCAF17"]
    COASY -->|"associated with"| DCAF17
    FA2H["FA2H"]
    COASY -->|"associated with"| FA2H
    C19ORF12["C19ORF12"]
    COASY -->|"associated with"| C19ORF12
    PANK2["PANK2"]
    COASY -->|"associated with"| PANK2
    PLA2G6["PLA2G6"]
    COASY -->|"associated with"| PLA2G6
    Lipid_Metabolism(["Lipid Metabolism"])
    COASY -->|"associated with"| Lipid_Metabolism
    Mitophagy(["Mitophagy"])
    COASY -->|"associated with"| Mitophagy
    Autophagy(["Autophagy"])
    COASY -->|"associated with"| Autophagy
    AKT["AKT"]
    AKT -->|"regulates"| COASY
    FTL["FTL"]
    FTL -->|"associated with"| COASY
    WDR45["WDR45"]
    WDR45 -->|"associated with"| COASY
    style COASY fill:#1a3a4a,stroke:#4fc3f7,stroke-width:3px,color:#e0e0e0

Outgoing (12)

TargetRelationTypeStr
Neurodegenerationassociated_withdisease0.65
Msassociated_withdisease0.65
Parkinsonassociated_withdisease0.65
Dystoniaassociated_withdisease0.65
DCAF17associated_withgene0.60

Incoming (2)

SourceRelationTypeStr
FTLassociated_withgene0.60
WDR45associated_withgene0.60

Targeting Hypotheses (0)

Hypotheses where this entity is a therapeutic target

HypothesisScoreDiseaseAnalysis
No targeting hypotheses

Mentioning Analyses (0)

Scientific analyses that reference this entity

No analyses mention this entity

Related Papers (0)

Scientific publications cited in analyses involving this entity

Title & PMIDAuthorsJournalYearCitations
No papers found