C1QC

OMIMHGNC

Synonym(s): C1QG

Locus: 1p36.12

 

Disorders

Tests

Test Type
Molecular (9)
Multi-Gene Panel (8)
Multi-Method Panel (3)
Test Method
Del/Dup (CNV) (3)
Sequencing, Capillary (Sanger) (1)
Sequencing, Next Gen (9)
Prenatal/Carrier
Prenatal (2)
Carrier (3)
Lab Location
USA(1)
Poland(1)
Germany(2)
Portugal(3)
Finland(2)
 
Kidney Diseases Panel
method(s): ◦ Sequencing, Next Gen 
Genomic Laboratory of the DNA Research Center LTD (Centrum Badań DNA sp z o.o.) - Poznań, Poland
TAT: 4-6 weeks
price: contact lab
C1q Deficiency Panel
method(s): ◦ Sequencing, Next Gen 
CeGaT GmbH - Tübingen, Germany
TAT: 4-6 weeks
price: contact lab
Complement Deficiencies Panel
method(s): ◦ Sequencing, Next Gen 
CeGaT GmbH - Tübingen, Germany
TAT: 4-5 Weeks
price: contact lab
C1QC
method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Fulgent Diagnostics - Temple City, CA, USA
Complement deficiencies � all subtypes (NGS panel of 33 genes)
method(s): ◦ Sequencing, Next Gen 
CGC Genetics - Porto, Portugal
Complement deficiencies � Low susceptibility to infections: SLE-like syndrome, atypical hemolytic uremic syndrome and others (NGS panel of 19 genes)
method(s): ◦ Sequencing, Next Gen 
CGC Genetics - Porto, Portugal
Complement deficiencies � SLE-like syndrome (NGS panel of 8 genes)
method(s): ◦ Sequencing, Next Gen 
CGC Genetics - Porto, Portugal
TAT: 3-4 weeks
price: contact lab
Primary Immunodeficiency Panel
method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen 
Blueprint Genetics - Helsinki, Finland
TAT: 3-4 weeks
price: contact lab
Complement System Disorder Panel
method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen 
Blueprint Genetics - Helsinki, Finland