Structured Summary
Abstract
A tight junction-associated MARVEL protein that may play a role in separating the endolymphatic and perilymphatic spaces of the ORGAN OF CORTI. Defects in the gene that codes for MARVELD2 protein are a cause of deafness autosomal recessive type 49.
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Synonyms
2 entry terms
- MARVELD2 Protein
- Tricellulin
MeSH Record
Aspects Covered
30 allowable subheadings
Indexed with the subheadings administration & dosage, adverse effects, agonists, analysis, antagonists & inhibitors, biosynthesis, blood, cerebrospinal fluid, chemical synthesis, chemistry, classification, deficiency, 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
2013
MeSH Record
Previous Indexing
- Membrane Proteins (2007-2012)
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AMA Style
References
- National Library of Medicine. MARVEL Domain Containing 2 Protein. Medical Subject Headings (MeSH). 2026. Unique ID D062794. http://id.nlm.nih.gov/mesh/2026/D062794
- MARVEL Domain Containing 2 Protein. In: Wikidata. https://www.wikidata.org/wiki/Q21120817