SH2B3

OMIMHGNC

Synonym(s): LNK, IDDM20

Locus: 12q24.12

Protein: SH2B adapter protein 3

 

Disorders

Tests

Test Type
Molecular (10)
Multi-Gene Panel (8)
Multi-Method Panel (2)
Test Method
Del/Dup (CNV) (2)
Sequencing, Capillary (Sanger) (3)
Genotyping (Microarray, Beads, etc.) (1)
Sequencing, Next Gen (8)
Prenatal/Carrier
Carrier (3)
Lab Location
Portugal(1)
USA(4)
Germany(1)
Spain(2)
Austria(2)
 
TAT: 2-3 weeks
price: contact lab
Cardiac DNA Inisight
method(s): ◦ Genotyping (Microarray, Beads, etc.) 
Pathway Genomics Corporation - San Diego, CA, USA
TAT: 2-3 weeks
price: contact lab
NGS HemeOnc Panel
method(s): ◦ Sequencing, Next Gen 
Diagnostic Labs at BloodCenter of Wisconsin - Milwaukee, WI, USA
Erythrocytosis, somatic (sequence analysis of SH2B3 gene)
method(s): ◦ Sequencing, Capillary (Sanger) 
CGC Genetics - Porto, Portugal
TAT: 4-6 weeks
price: contact lab
Erythrocytes, Anemia Panel
method(s): ◦ Sequencing, Next Gen 
CeGaT GmbH - Tübingen, Germany
Myelofibrosis NGS panel
method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen 
Fulgent Diagnostics - Temple City, CA, USA
TAT: 4-5 Weeks
price: contact lab
SH2B3
method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Fulgent Diagnostics - Temple City, CA, USA
Bone Marrow Failure Related Disorders, Panel Massive Sequencing (NGS) 61 Genes
method(s): ◦ Sequencing, Next Gen 
Reference Laboratory Genetics - Hospitalet de Llobregat, Spain
Erythrocytosis, familial/ Polycythemia (Polyzythämie/ Erythrozytose)
method(s): ◦ Sequencing, Next Gen 
Praxis fuer Humangenetik Wien - Vienna, Austria
Somatic Myelofibrosis, Panel Massive Sequencing (NGS) 4 Genes
method(s): ◦ Sequencing, Next Gen 
Reference Laboratory Genetics - Hospitalet de Llobregat, Spain
Erythrocytosis (Erythrozytosis)
method(s): ◦ Sequencing, Next Gen 
Praxis fuer Humangenetik Wien - Vienna, Austria