Chemicals and Drugs

Wiskott-Aldrich Syndrome Protein

WASP protein is mutated in WISKOTT-ALDRICH SYNDROME and is expressed primarily in hematopoietic cells. It is the founding member of the WASP protein family and interacts with CDC42 PROTEIN to help regulate ACTIN polymerization.

National Library of MedicineMedical Subject Headings2026

Structured Summary

Abstract

WASP protein is mutated in WISKOTT-ALDRICH SYNDROME and is expressed primarily in hematopoietic cells. It is the founding member of the WASP protein family and interacts with CDC42 PROTEIN to help regulate ACTIN polymerization.

MeSH Record

Classification

Broader headings

Related Concepts

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MeSH Record

Synonyms

2 entry terms
  • WASP Protein
  • Wiskott Aldrich Syndrome Protein

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

Indexing Annotation

WISKOTT-ALDRICH SYNDROME PROTEIN FAMILY and WISKOTT-ALDRICH SYNDROME PROTEIN, NEURONAL are also available

MeSH Record

History Note

2006(1994)

MeSH Hierarchy

Tree Numbers

  1. D05.750w.078w.730.912.500
  2. D12.776w.220.525.912.500

AMA Style

References

  1. National Library of Medicine. Wiskott-Aldrich Syndrome Protein. Medical Subject Headings (MeSH). 2026. Unique ID D051316. http://id.nlm.nih.gov/mesh/2026/D051316
  2. Wiskott-Aldrich Syndrome Protein. In: Wikidata. https://www.wikidata.org/wiki/Q24788128