gene

NIPA1

Entity Detail — Knowledge Graph Node

Understanding Entity Pages

This page aggregates everything SciDEX knows about NIPA1: 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.

3Connections
0Hypotheses
0Analyses
1Outgoing
2Incoming

Summary

Page for NIPA1 Gene

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🧬 Gene Info
Gene SymbolNIPA1
Full NameNon-imprinted in Prader-Willi/Angelman Syndrome 1
Chromosome9q21.13
Protein TypeTransporter
Functionencodes a magnesium transporter protein that plays critical roles in neuronal function, synaptic transmission, and intracellular magnesium homeostasis.
Amino Acids317 aa
UniProt ID[Q9BUE2](https://www.uniprot.org/uniprot/Q9BUE2)
Ensembl IDENSG00000139970
GeneCardsNIPA1
Human Protein AtlasNIPA1
Ion SpecificityHighly selective for magnesium over other divalent cations
Transport MechanismElectrogenic Mg²⁺/H⁺ antiport mechanism
pH SensitivityActivity modulated by intracellular pH
RegulationControlled by cellular magnesium status and neuronal activity
Associated Diseasesneurodegeneration
KG Connections3 knowledge graph edges
DatabasesGeneCardsNCBI GeneHPASTRING

Wiki Pages (3)

Knowledge base pages for this entity

Canonical Page

NIPA1 Gene

gene · 988 words

hereditary-spastic-paraplegia

disease · 2618 words

Genes

index · 271 words

Pathway Diagram

flowchart TD
    N0["NIPA1"]
    N1["ATXN1"]
    N1 -->|"associated with"| N0
    N2["ATXN2"]
    N2 -->|"associated with"| N0
    N3["UNC13A"]
    N0 -->|"associated with"| N3
    N4["neurodegeneration"]
    N0 -->|"implicated in"| N4

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    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
    classDef drug fill:#1a2a2a,stroke:#26c6da,color:#e0e0e0
    classDef cell_type fill:#2a1a2a,stroke:#ab47bc,color:#e0e0e0
    classDef phenotype fill:#2a2a1a,stroke:#ffa726,color:#e0e0e0
    classDef process fill:#1a2a2a,stroke:#66bb6a,color:#e0e0e0
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    classDef therapeutic fill:#1a2a2a,stroke:#26c6da,color:#e0e0e0
    classDef index fill:#1a1a2a,stroke:#7986cb,color:#e0e0e0
    class N0 gene
    class N1 gene
    class N2 gene
    class N3 gene

Outgoing (1)

TargetRelationTypeStr
UNC13Aassociated_withgene0.60

Incoming (2)

SourceRelationTypeStr
ATXN1associated_withgene0.60
ATXN2associated_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