gene

VPS13A

Entity Detail — Knowledge Graph Node

Understanding Entity Pages

This page aggregates everything SciDEX knows about VPS13A: 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.

6Connections
0Hypotheses
0Analyses
4Outgoing
2Incoming

Summary

Page for VPS13A

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🧬 Gene Info
Gene SymbolVPS13A
Full NameVacuolar Protein Sorting 13 Homolog A
Chromosome9q21.13
FunctionVPS13A encodes a member of the vacuolar protein sorting 13 (VPS13) family of proteins, which are involved in membrane trafficking between organelles.
Primary Expressionthe brain, with high expression in the basal ganglia (caudate nucleus, putamen), cerebral cortex, and cerebellum
Molecular Weight350 kDa
Amino Acids3179 aa
UniProt IDQ9UPQ3
NCBI Gene ID23286
Ensembl IDENSG00000140320
OMIM216950
GeneCardsVPS13A
Human Protein AtlasVPS13A
VPS13B, VPS13C, VPS13DRelated lipid transport proteins with distinct tissue distributions and roles in Cohen syndrome and other lipid storage disorders
ERMES ComplexER-mitochondrial encounter structure components that functionally interact with VPS13A
Associated DiseasesHuntington's disease, neurodegeneration
InteractionsXK
KG Connections6 knowledge graph edges
DatabasesGeneCardsHPASTRING
🔮 Predicted Structure: VPS13A — AlphaFold Q9UPQ3 Click to expand

AI-predicted structure from AlphaFold | Powered by Mol*

Wiki Pages (16)

Knowledge base pages for this entity

Canonical Page

VPS13A

gene · 667 words

Creatine for Neuroprotection

therapeutic · 3742 words

Mitochondria-Lysosome Contact Site Dysfunction in Parkinson's Disease

mechanism · 3314 words

Neuroacanthocytosis Syndromes

disease · 3156 words

VPS13C Protein

protein · 2807 words

huntingtons-disease-like-1

disease · 2647 words

Pathway Diagram

flowchart TD
    N0["VPS13A"]
    N1["XK"]
    N1 -->|"interacts with"| N0
    N2["neurodegeneration"]
    N0 -->|"implicated in"| N2

    classDef gene fill:#1a3a2a,stroke:#4caf50,color:#e0e0e0
    classDef protein fill:#1a2a3a,stroke:#4fc3f7,color:#e0e0e0
    classDef disease fill:#3a1a1a,stroke:#ef5350,color:#e0e0e0
    classDef pathway fill:#2a1a3a,stroke:#ce93d8,color:#e0e0e0
    classDef mechanism fill:#2a2a1a,stroke:#ffd54f,color:#e0e0e0
    class N1 gene

Outgoing (4)

TargetRelationTypeStr
ferroptosisparticipates_inpathway0.60
neurodegenerationcausesdisease0.60
Huntington's diseasecausesdisease0.60
oxidative stress responseparticipates_inpathway0.60

Incoming (2)

SourceRelationTypeStr
XKinteracts_withgene0.90
GPX4translocates_togene0.60

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