MID2

OMIMHGNC

Synonym(s): FXY2, TRIM1, RNF60, MRX101

Locus: Xq22.3

Protein: Probable E3 ubiquitin-protein ligase MID2

 

Disorders

Tests

Test Type
Molecular (5)
Multi-Gene Panel (3)
Multi-Method Panel (2)
Test Method
Del/Dup (CNV) (4)
Sequencing, Capillary (Sanger) (2)
Sequencing, Next Gen (4)
Prenatal/Carrier
Carrier (1)
Lab Location
USA(3)
Portugal(1)
Germany(1)
 
TAT: 8-9 weeks
price: contact lab
Mental retardation, X-linked (NGS panel for 89 genes)
method(s): ◦ Sequencing, Next Gen 
CGC Genetics - Porto, Portugal
TAT: 2-4 weeks
price: contact lab
Nonsyndromic Intellectual Disability (NextGen Sequencing Panel and Copy Number Analysis; 81 genes)
method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen 
MNG Laboratories (Medical Neurogenetics, LLC.) - Atlanta, GA, USA
TAT: 2-4 weeks
price: contact lab
Comprehensive Intellectual Disability (NextGen Sequencing Panel and Copy Number Analysis; 349 Genes)
method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen 
MNG Laboratories (Medical Neurogenetics, LLC.) - Atlanta, GA, USA
TAT: 4-5 Weeks
price: contact lab
MID2
method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Fulgent Diagnostics - Temple City, CA, USA
TAT: 3-4 weeks
price: contact lab
Mental retardation, X-linked type 101
method(s): ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Centogene AG, Rare Disease Company - Rostock, Germany