EFHC2

OMIMHGNC

Synonym(s): FLJ22843, MRX74

Locus: Xp11.3

Protein: EF-hand domain-containing family member C2

Tests

Test Type
Molecular (3)
Multi-Gene Panel (1)
Multi-Method Panel (3)
Test Method
Del/Dup (CNV) (3)
Sequencing, Capillary (Sanger) (3)
Sequencing, Next Gen (2)
Prenatal/Carrier
Carrier (2)
Lab Location
USA(2)
Germany(1)
 
TAT: 4-5 Weeks
price: contact lab
EFHC2
method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Fulgent Diagnostics - Temple City, CA, USA
TAT: 3-4 weeks
price: contact lab
Comprehensive Epilepsy Panel
method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen 
Fulgent Diagnostics - Temple City, CA, USA
TAT: 3-4 weeks
price: contact lab
Mental retardation, x-linked, EFHC2 related
method(s): ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Centogene AG, Rare Disease Company - Rostock, Germany