gene

SLC41A1

Entity Detail — Knowledge Graph Node

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This page aggregates everything SciDEX knows about SLC41A1: 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

SLC41A1 is a magnesium transporter protein implicated in early-onset Parkinson's disease, renal magnesium wasting, and neuronal magnesium homeostasis critical for mitochondrial function

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🧬 Gene Info

Gene Symbol	SLC41A1
Full Name	Solute Carrier Family 41 Member 1
Chromosome	17q23
Protein Type	Transporter
Function	is a member of the SLC41 family of magnesium transporters that plays a critical role in cellular magnesium homeostasis.
Primary Expression	Brain (substantia nigra), kidney, heart, liver, skeletal muscle
Amino Acids	515 aa
UniProt ID	[Q9H3M4](https://www.uniprot.org/uniprot/Q9H3M4)
Ensembl ID	ENSG00000133043
OMIM	610264
GeneCards	SLC41A1
Human Protein Atlas	SLC41A1
Associated Diseases	Parkinson's disease, Alzheimer's disease
Databases	GeneCards NCBI Gene HPA STRING

Wiki Pages (1)

Knowledge base pages for this entity

Canonical Page

SLC41A1 — Solute Carrier Family 41 Member 1

gene · 1809 words

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Pathway Diagram

graph TD
    SLC41A1["SLC41A1"]
    neurodegeneration["neurodegeneration"]
    SLC41A1 -->|"implicated_in"| neurodegeneration
    style SLC41A1 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)

Scientific analyses that reference this entity

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Experiments (0)

Experimental studies targeting or related to this entity

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Related Papers (0)

Scientific publications cited in analyses involving this entity

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Debates (0)

Multi-agent debates referencing this entity

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Related Research

Hypotheses and analyses mentioning SLC41A1 in their description or question text

No additional research found