gene

SPG35

Entity Detail — Knowledge Graph Node

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This page aggregates everything SciDEX knows about SPG35: 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.

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Summary

Page for SPG35 Gene

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🧬 Gene Info
Gene SymbolSPG35
Full NameFA2H (Fatty Acid 2-Hydroxylase)
Chromosome16q23.3
Functionis a member of the fatty acid hydroxylase family and plays a vital role in maintaining myelin integrity in the central nervous system (CNS) [@myelin_lipids_2011].
Subcellular Localizations and enzymatic activities, which could explain the tissue-specific phenotype of FA2H-related disorders
Molecular Weight44 kDa
Amino Acids383 aa
Exons13
UniProt ID[Q8IWA4](https://www.uniprot.org/uniprotkb/Q8IWA4/entry)
GeneCardsSPG35
Human Protein AtlasSPG35
Isoform 1 (canonical)Full-length 383 amino acids, predominantly expressed in brain
Isoform 2Lacks exon 6, expressed in peripheral tissues
Isoform 3Alternative start site, truncated variant
Substrate specificityPrefers C24 and C26 fatty acids
Associated Diseasesneurodegeneration
DatabasesGeneCardsNCBI GeneHPASTRING

Wiki Pages (1)

Knowledge base pages for this entity

Canonical Page

SPG35 Gene

gene · 2714 words

Pathway Diagram

graph TD
    SPG35["SPG35"]
    neurodegeneration["neurodegeneration"]
    SPG35 -->|"implicated_in"| neurodegeneration
    style SPG35 fill:#4a1a6b,stroke:#4fc3f7,stroke-width:2px,color:#e0e0e0

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Targeting Hypotheses (0)

Hypotheses where this entity is a therapeutic target

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Mentioning Analyses (0)

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Experiments (0)

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Related Papers (0)

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Debates (0)

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Related Research

Hypotheses and analyses mentioning SPG35 in their description or question text

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