Structured Summary
Abstract
An SMN complex protein that contains a TUDOR DOMAIN and is essential for the function of the SMN protein complex. In humans, the protein is encoded by a single gene found near the inversion TELOMERE of a large inverted region of CHROMOSOME 5. Mutations in the gene coding for survival of motor neuron 1 protein may result in SPINAL MUSCULAR ATROPHIES OF CHILDHOOD.
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Classification
Broader headings
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Synonyms
3 entry terms
- SMN Protein (Spinal Muscular Atrophy)
- Survival Motor Neuron Protein 1
- Survival of Motor Neuron 1, Telomeric Protein
MeSH Record
Aspects Covered
29 allowable subheadings
Indexed with the subheadings administration & dosage, adverse effects, agonists, analysis, antagonists & inhibitors, biosynthesis, blood, cerebrospinal fluid, chemical synthesis, chemistry, classification, drug effects, economics, genetics, history, immunology, isolation & purification, metabolism, pharmacokinetics, pharmacology, physiology, poisoning, radiation effects, standards, supply & distribution, therapeutic use, toxicity, ultrastructure, urine.
MeSH Record
History Note
2009(2005); use SMN COMPLEX PROTEINS 2005-2008
MeSH Record
Previous Indexing
- SMN Complex Proteins (2005-2008)
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Tree Numbers
AMA Style
References
- National Library of Medicine. Survival of Motor Neuron 1 Protein. Medical Subject Headings (MeSH). 2026. Unique ID D055533. http://id.nlm.nih.gov/mesh/2026/D055533
- Survival of Motor Neuron 1 Protein. In: Wikidata. https://www.wikidata.org/wiki/Q21111707