Disorders


 

X-Linked Mental Retardation 21


Synonym(s): MRX21, MRX34, X-Linked Mental Retardation 34

 

OMIM

GeneLocusProtein
IL1RAPL1Xp22.1-p21.3X-linked interleukin-1 receptor accessory protein-like 1

Laboratory Test Method Prenatal Carrier *
Ambry Genetics Corp, Ambry Genetics - Aliso Viejo, CA, USA• Sequence analysis of the entire coding region
• Deletion/duplication analysis
  
Centogene AG, Rare Disease Company - Rostock, Germany• Sequence analysis of the entire coding region
 
Emory University School of Medicine, Emory Molecular Genetics Laboratory - Atlanta, GA, USA• Sequence analysis of the entire coding region
• Deletion/duplication analysis
PerkinElmer, Signature Genomic Laboratories - Spokane, WA, USA• FISH-metaphase
 

* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.

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