chromosome Xp21 deletion syndrome

Summary
Synonym
  • Xp21 microdeletion syndrome
  • complex glycerol kinase deficiency
  • monosomy Xp21
Definition
A chromosomal deletion syndrome that has_material_basis_in deletion of the chromosome Xp21 region.
Super Class
chromosomal deletion syndrome
External Links
Disease Ontology
DOID:0060427
Mondo Disease Ontology
ORDO
OMIM
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
2710 GK glycerol kinase
11141 IL1RAPL1 interleukin 1 receptor accessory protein like 1
Related Glycoprotein
Displaying all 2 entries
UniProt ID Protein Name Source
P32189 Glycerol kinase
Q9NZN1 Interleukin-1 receptor accessory protein-like 1

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024