Structured Summary
Abstract
Transmembrane proteins belonging to the tumor necrosis factor superfamily that play an essential role in the normal development of several ectodermally derived organs. Several isoforms of the ectodysplasins exist due to multiple ALTERNATIVE SPLICING of the MRNA for the protein. The isoforms ectodysplasin A1 and ectodysplasin A2 are considered biologically active and each bind distinct ECTODYSPLASIN RECEPTORS. Genetic mutations that result in loss of function of ectodysplasin result in ECTODERMAL DYSPLASIA 1, ANHIDROTIC.
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Synonyms
7 entry terms
- Ectodysplasin
- Ectodysplasin-A
- Ectodysplasin A
- Ectodysplasin A, Isoform 1
- Ectodysplasin A, Isoform 2
- Ectodysplasin A1
- Ectodysplasin A2
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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.
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History Note
2007(1999)
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References
- National Library of Medicine. Ectodysplasins. Medical Subject Headings (MeSH). 2026. Unique ID D053331. http://id.nlm.nih.gov/mesh/2026/D053331
- Ectodysplasins. In: Wikidata. https://www.wikidata.org/wiki/Q76715386