Structured Summary
Abstract
A homeodomain protein that is highly expressed in the nuclei of skeletal muscle, bone marrow, and osteogenic cells and has critical roles in growth and development. Its gene resides within PSEUDOAUTOSOMAL REGION 1 of X and Y chromosomes and mutations are associated with several growth disorders including LERI-WEIL SYNDROME; LANGER MESOMELIC DYSPLASIA; and SHORT STATURE, IDIOPATHIC, X-LINKED.
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Classification
Broader headings
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Synonyms
4 entry terms
- GCFX Protein
- PHOG Protein
- SHOX Protein
- SHOXY 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
History Note
2018
MeSH Record
Previous Indexing
- Homeodomain Proteins (1997-2017)
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Tree Number
AMA Style
References
- National Library of Medicine. Short Stature Homeobox Protein. Medical Subject Headings (MeSH). 2026. Unique ID D000074122. http://id.nlm.nih.gov/mesh/2026/D000074122
- Short Stature Homeobox Protein. In: Wikipedia. https://en.wikipedia.org/wiki/Short-stature_homeobox_gene
- Short Stature Homeobox Protein. In: Wikidata. https://www.wikidata.org/wiki/Q2206154