Integrin, Beta-3; Itgb3

Description

The ITGB3 gene encodes glycoprotein IIIa (GP IIIa), the beta subunit of the platelet membrane adhesive protein receptor complex GP IIb/IIIa. The alpha subunit, GP IIb, is encoded by the ITGA2B gene (OMIM ). The GP IIb/IIIa complex belongs to the integrin class of cell adhesion molecule receptors that share a common heterodimeric structure with alpha and beta subunits (summary by Bray et al., 1987 and Bajt et al., 1992).Glycoprotein IIIa is also the beta subunit of 2 other integrins, fibronectin receptor (FNRB ) and vitronectin receptor (OMIM ), which have distinctive alpha subunits.

Clinical Features

Top most frequent phenotypes and symptoms related to Integrin, Beta-3; Itgb3

  • Anemia
  • Neoplasm
  • Thrombocytopenia
  • Bruising susceptibility
  • Gastrointestinal hemorrhage
  • Epistaxis
  • Purpura
  • Intracranial hemorrhage
  • Abnormality of coagulation
  • Menorrhagia
And another 6 symptoms. If you need more information about this disease we can help you.
Click here to know more about Mendelian.

Incidence and onset information

— Based on the latest data available Integrin, Beta-3; Itgb3 have a estimated prevalence of 0 per 100k worldwide.


Mendelian

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Integrin, Beta-3; Itgb3 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Platelet Antigen Genotyping Panel.

By BloodCenter of Wisconsin Diagnostic Laboratories BloodCenter of Wisconsin, part of Versiti in United States.

GP1BA, ITGA2, ITGB3, ITGA2B, CD109
Specificity
100 %
Genes
84 %
CD109.

By Fulgent Genetics Fulgent Genetics in United States.

CD109
Specificity
100 %
Genes
17 %
Platelet Disorders.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

RUNX1, DTNBP1, HPS1, HPS6, HPS5, HPS4, HPS3, AP3B1, ANKRD26, DPAGT1, MPL, WAS, FLNA, MYH9, GATA1, BLOC1S6, LYST, VWF, GNAS, F8 , (...)

View the complete list with 35 more genes
Specificity
8 %
Genes
67 %
ITGA2.

By Institute for Human Genetics University Clinic Freiburg in Germany.

ITGA2
Specificity
100 %
Genes
17 %
Bleeding Disorders Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

F2, F5, RUNX1, DTNBP1, HPS1, BLOC1S3, HPS6, HPS5, HPS4, HPS3, CYCS, AP3B1, ANKRD26, MPL, WAS, FLNA, MYH9, GATA1, F11, VWF , (...)

View the complete list with 41 more genes
Specificity
9 %
Genes
84 %
Platelet Function Disorder Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

DTNBP1, HPS1, BLOC1S3, HPS6, HPS5, HPS4, HPS3, AP3B1, GP1BA, ANO6, GP6, TBXA2R, P2RX1, P2RY12, TBXAS1, PLAU, ITGA2, CD36, ITGB3, ITGA2B , (...)

View the complete list with 2 more genes
Specificity
23 %
Genes
84 %
Glycoprotein Ia C807T polymorphism.

By Centogene AG - the Rare Disease Company in Germany.

ITGA2
Specificity
100 %
Genes
17 %
Glycoprotein 1a Deficiency (ITGA2).

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

ITGA2
Specificity
100 %
Genes
17 %
ITGA2.

By Fulgent Genetics Fulgent Genetics in United States.

ITGA2
Specificity
100 %
Genes
17 %
Thrombocytopenia Panel.

By Blueprint Genetics in Finland.

RUNX1, CYCS, ANKRD26, MPL, WAS, FLNA, MYH9, GATA1, THBD, ADAMTS13, ABCG5, ABCG8, GP1BA, NBEAL2, ITGA2, HOXA11, GFI1B, ITGB3, ITGA2B, MASTL , (...)

View the complete list with 14 more genes
Specificity
15 %
Genes
84 %
Comprehensive Hematology Panel.

By Blueprint Genetics in Finland.

BRCA1, BRCA2, F2, F5, HFE, EPCAM, MSH2, PMS2, MSH6, MLH1, RECQL4, RUNX1, TP53, YARS2, PC, HBB, TYRP1, OCA2, AMN, SLC45A2 , (...)

View the complete list with 219 more genes
Specificity
3 %
Genes
84 %
Thrombocytopenia Sequencing Panel.

By Genetic Services Laboratory University of Chicago in United States.

CYCS, ANKRD26, GATA2, MPL, WAS, FLNA, MYH9, GATA1, TERC, TERT, VWF, CFB, CFI, CFH, CFHR5, CD46, C3, THBD, CFHR1, CFHR3 , (...)

View the complete list with 23 more genes
Specificity
10 %
Genes
67 %
Thrombocytopenia Deletion/Duplication Panel.

By Genetic Services Laboratory University of Chicago in United States.

RUNX1, CYCS, ANKRD26, GATA2, MPL, WAS, FLNA, MYH9, GATA1, TERC, TERT, VWF, CFB, CFI, CFH, CFHR5, CD46, C3, THBD, CFHR1 , (...)

View the complete list with 23 more genes
Specificity
10 %
Genes
67 %
Bernard Soulier Syndrome.

By Institute of Human Genetics Universitätsmedizin Greifswald in Germany.

GP1BA, GP1BB, GP9
Specificity
67 %
Genes
34 %
VWD Platelet Type (GP1BA) 4 Mutations.

By ARUP Laboratories, Molecular Genetics and Genomics in United States.

GP1BA
Specificity
100 %
Genes
17 %
Bernard-Soulier syndrome.

By Sheffield Diagnostic Genetics Service Sheffield Children's NHS Foundation Trust in United Kingdom.

GP1BA, GP1BB, GP9
Specificity
67 %
Genes
34 %
GP1BA. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

GP1BA
Specificity
100 %
Genes
17 %
Bernard-Soulier syndrome (sequence analysis of GP1BA gene).

By CGC Genetics in Portugal.

GP1BA
Specificity
100 %
Genes
17 %
Bernard-Soulier syndrome, type A.

By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders in Germany.

GP1BA
Specificity
100 %
Genes
17 %
Pseudo von Willebrand disease.

By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders in Germany.

GP1BA
Specificity
100 %
Genes
17 %
BERNARD-SOULIER SYNDROME.

By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders in Germany.

GP1BA, GP1BB, GP9
Specificity
67 %
Genes
34 %
Thrombocytopenia Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

RUNX1, CYCS, ANKRD26, MPL, WAS, MYH9, GATA1, ADAMTS13, GP1BA, MASTL, GP1BB, GP9
Specificity
17 %
Genes
34 %
Bernard-Soulier Syndrome via GP1BA Gene Sequencing with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

GP1BA
Specificity
100 %
Genes
17 %
Thrombocytopenia Sequencing Panel with CNV Detection - Expanded.

By PreventionGenetics PreventionGenetics in United States.

RUNX1, CYCS, ANKRD26, MPL, WAS, FLNA, MYH9, GATA1, ADAMTS13, ABCG5, ABCG8, GP1BA, NBEAL2, HOXA11, GFI1B, CD36, ITGB3, ITGA2B, MASTL, ETV6 , (...)

View the complete list with 9 more genes
Specificity
14 %
Genes
67 %
Platelet bleeding disorders NGS panel.

By Connective Tissue Gene Tests in United States.

DTNBP1, SMPD1, HPS1, BLOC1S3, HPS6, HPS5, HPS4, HPS3, AP3B1, GBA, WAS, MYH9, BLOC1S6, LYST, VWF, GP1BA, ANO6, GP6, TBXA2R, P2RY12 , (...)

View the complete list with 14 more genes
Specificity
12 %
Genes
67 %
Platelet bleeding disorders Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

DTNBP1, SMPD1, HPS1, BLOC1S3, HPS6, HPS5, HPS4, HPS3, AP3B1, GBA, WAS, MYH9, BLOC1S6, LYST, VWF, GP1BA, ANO6, GP6, TBXA2R, P2RY12 , (...)

View the complete list with 14 more genes
Specificity
12 %
Genes
67 %
Platelet bleeding disorders Comprehensive panel.

By Connective Tissue Gene Tests in United States.

DTNBP1, SMPD1, HPS1, BLOC1S3, HPS6, HPS5, HPS4, HPS3, AP3B1, GBA, WAS, MYH9, BLOC1S6, LYST, VWF, GP1BA, ANO6, GP6, TBXA2R, P2RY12 , (...)

View the complete list with 14 more genes
Specificity
12 %
Genes
67 %
Bernard-Soulier Panel.

By FirmaLab in United States.

GP1BA, GP1BB, GP9
Specificity
67 %
Genes
34 %
Bernard Soulier syndrome type A1.

By Centogene AG - the Rare Disease Company in Germany.

GP1BA
Specificity
100 %
Genes
17 %
Bernard Soulier syndrome type A2.

By Centogene AG - the Rare Disease Company in Germany.

GP1BA
Specificity
100 %
Genes
17 %
Thrombocytopenia panel.

By Centogene AG - the Rare Disease Company in Germany.

RUNX1, MPL, WAS, MYH9, GATA1, ADAMTS13, GP1BA, ITGB3, ITGA2B, MASTL, GP1BB, GP9
Specificity
34 %
Genes
67 %
von Willebrand disease platelet type.

By Centogene AG - the Rare Disease Company in Germany.

GP1BA
Specificity
100 %
Genes
17 %
Nonarteritic anterior ischemic optic neuropathy.

By Centogene AG - the Rare Disease Company in Germany.

GP1BA
Specificity
100 %
Genes
17 %
AllNeuro panel.

By Centogene AG - the Rare Disease Company in Germany.

F2, F5, FMR1, HTT, HFE, MTHFR, TTR, UBE3A, VHL, PTEN, AARS2, ABHD12, ACACA, ACAD9, ACADL, ACADM, ACADS, AGL, ACADVL, ACAT1 , (...)

View the complete list with 1185 more genes
Specificity
1 %
Genes
17 %
CentoICU platinum plus.

By Centogene AG - the Rare Disease Company in Germany.

BRCA2, F2, F5, MTHFR, UBE3A, MCCC1, MCCC2, AARS2, ACAD9, ACADL, ACADM, ACADS, AGL, ACADVL, ACAT1, ALDOA, ALDOB, FBP1, PC, GYS2 , (...)

View the complete list with 494 more genes
Specificity
1 %
Genes
50 %
CentoICU platinum.

By Centogene AG - the Rare Disease Company in Germany.

BRCA2, F2, F5, MTHFR, UBE3A, MCCC1, MCCC2, AARS2, ACAD9, ACADL, ACADM, ACADS, AGL, ACADVL, ACAT1, ALDOA, ALDOB, FBP1, PC, GYS2 , (...)

View the complete list with 494 more genes
Specificity
1 %
Genes
50 %
Bernard Soulier Syndrome.

By Molecular Haemostasis & Thrombosis GSTS Pathology - Guy's and St. Thomas' NHS Foundation Trust in United Kingdom.

GP1BA, GP1BB, GP9
Specificity
67 %
Genes
34 %
Bernard-Soulier syndrome A.

By Medical Genetics Laboratory Diagenom GmbH in Germany.

GP1BA
Specificity
100 %
Genes
17 %
Thrombocytopenia Panel.

By CeGaT GmbH in Germany.

AP3B1, MPL, MYH9, GATA1, THBD, ADAMTS13, GP1BA, ITGB3, ITGA2B, MASTL, GP1BB, RBM8A, GP9
Specificity
31 %
Genes
67 %
Thrombocytopenia.

By Asper Biogene Asper Biogene LLC in Estonia.

RUNX1, CYCS, ANKRD26, MPL, WAS, MYH9, GATA1, ADAMTS13, GP1BA, ITGA2B, MASTL, GP1BB, GP9
Specificity
24 %
Genes
50 %
VWD Platelet-Type Sequence Analysis.

By BloodCenter of Wisconsin Diagnostic Laboratories BloodCenter of Wisconsin, part of Versiti in United States.

GP1BA
Specificity
100 %
Genes
17 %
Bernard-Soulier Syndrome Sequence Analysis.

By BloodCenter of Wisconsin Diagnostic Laboratories BloodCenter of Wisconsin, part of Versiti in United States.

GP1BA, GP1BB, GP9
Specificity
67 %
Genes
34 %
aCGH Deletion/Duplication Analysis.

By BloodCenter of Wisconsin Diagnostic Laboratories BloodCenter of Wisconsin, part of Versiti in United States.

F2, F5, RUNX1, COL1A1, HPS1, BLOC1S3, HPS6, HPS5, HPS4, HPS3, CYCS, HAX1, ENG, MPL, WAS, LMNA, MYH9, GATA1, BLOC1S6, ACVRL1 , (...)

View the complete list with 45 more genes
Specificity
4 %
Genes
34 %
Bernard-Soulier syndrome A1.

By Praxis fuer Humangenetik Wien in Austria.

GP1BA
Specificity
100 %
Genes
17 %
Bernard-Soulier syndrome A2.

By Praxis fuer Humangenetik Wien in Austria.

GP1BA
Specificity
100 %
Genes
17 %
von Willebrand disease, platelet-type.

By Praxis fuer Humangenetik Wien in Austria.

GP1BA
Specificity
100 %
Genes
17 %
Bernard-Soulier Syndrome Type A.

By Regional Molecular Haemostasis Laboratory Birmingham Childrens Hospital NHS Foundation Trust in United Kingdom.

GP1BA
Specificity
100 %
Genes
17 %
Pseudo-von Willebrand Disease.

By Regional Molecular Haemostasis Laboratory Birmingham Childrens Hospital NHS Foundation Trust in United Kingdom.

GP1BA
Specificity
100 %
Genes
17 %
Bernard-Soulier syndrome A1.

By MedGene in Slovakia.

GP1BA
Specificity
100 %
Genes
17 %
Bernard-Soulier syndrome A2.

By MedGene in Slovakia.

GP1BA
Specificity
100 %
Genes
17 %
von Willebrand disease, platelet-type.

By MedGene in Slovakia.

GP1BA
Specificity
100 %
Genes
17 %
Thrombocytopenia NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

RUNX1, MPL, WAS, MYH9, GATA1, ADAMTS13, GP1BA, MASTL, GP1BB, GP9
Specificity
20 %
Genes
34 %
Coagulation NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

VWF, F9, F8, GP1BA
Specificity
25 %
Genes
17 %
GP1BA.

By Fulgent Genetics Fulgent Genetics in United States.

GP1BA
Specificity
100 %
Genes
17 %
Platelet Function Disorder Panel.

By Blueprint Genetics in Finland.

RUNX1, DTNBP1, HPS1, BLOC1S3, HPS6, HPS5, HPS4, HPS3, AP3B1, BLOC1S6, THPO, GP1BA, TBXA2R, P2RY12, NBEAL2, ITGB3, ITGA2B, GP1BB, WIPF1, GP9 , (...)

View the complete list with 1 more genes
Specificity
20 %
Genes
67 %
Bleeding Disorder/Coagulopathy Panel.

By Blueprint Genetics in Finland.

F2, F5, RUNX1, DTNBP1, HPS1, BLOC1S3, HPS6, HPS5, HPS4, HPS3, CYCS, AP3B1, ANKRD26, MPL, WAS, FLNA, MYH9, GATA1, BLOC1S6, F11 , (...)

View the complete list with 42 more genes
Specificity
7 %
Genes
67 %
Genetic Study of Hereditary Thrombophilia (11 genes).

By HeartGenetics, Genetics and Biotechnology, SA in Portugal.

F2, F5, MTHFR, GP1BA, SERPINE1, PROS1, F12, F13A1, SERPINC1, PROCR
Specificity
10 %
Genes
17 %
BERNARD-SOULIER SYNDROME.

By Laboratorio de Genetica Clinica SL in Spain.

GP1BA, GP1BB, GP9
Specificity
67 %
Genes
34 %
Bernard-Soulier Syndrome Type A2 , Sequencing GP1BA Gene.

By Reference Laboratory Genetics in Spain.

GP1BA
Specificity
100 %
Genes
17 %
Bernard-Soulier Syndrome Type A1 , Sequencing GP1BA Gene.

By Reference Laboratory Genetics in Spain.

GP1BA
Specificity
100 %
Genes
17 %
Bleeding Disorders , Panel Massive Sequencing (NGS) 23 Genes.

By Reference Laboratory Genetics in Spain.

F2, F5, MTHFR, F11, VWF, F9, F8, ADAMTS13, GP1BA, FGA, FGB, FGG, ITGB3, ITGA2B, GP1BB, F7, GP9, F10, F12, F13A1 , (...)

View the complete list with 2 more genes
Specificity
19 %
Genes
67 %
Thrombocytopenia and Related Disorders , Panel Massive Sequencing (NGS) 14 Genes.

By Reference Laboratory Genetics in Spain.

RUNX1, CYCS, ANKRD26, MPL, WAS, MYH9, GATA1, ADAMTS13, GP1BA, ITGB3, ITGA2B, JAK2, GP1BB, SRC, GP9
Specificity
27 %
Genes
67 %
Bernard-Soulier Syndrome , Panel Massive Sequencing (NGS) GP9, GP1BA, GP1BB Genes.

By Reference Laboratory Genetics in Spain.

GP1BA, GP1BB, GP9
Specificity
67 %
Genes
34 %
Platelet Function Related Disorders , Panel Massive Sequencing (NGS) 17 Genes.

By Reference Laboratory Genetics in Spain.

DTNBP1, HPS1, BLOC1S3, HPS6, HPS5, HPS4, HPS3, AP3B1, GP1BA, ANO6, GP6, TBXA2R, P2RY12, ITGB3, ITGA2B, GP1BB, GP9
Specificity
24 %
Genes
67 %
Glanzmann thrombasthenia.

By Institute of Human Genetics Universitätsmedizin Greifswald in Germany.

ITGB3, ITGA2B
Specificity
100 %
Genes
34 %
Glanzmann thrombasthenia.

By Sheffield Diagnostic Genetics Service Sheffield Children's NHS Foundation Trust in United Kingdom.

ITGB3, ITGA2B
Specificity
100 %
Genes
34 %
ITGB3. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

ITGB3
Specificity
100 %
Genes
17 %
Fetal and neonatal alloimmune thrombocytopenia (sequence analysis of ITGB3 gene).

By CGC Genetics in Portugal.

ITGB3
Specificity
100 %
Genes
17 %
Glanzmann's thrombasthenia.

By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders in Germany.

ITGB3, ITGA2B
Specificity
100 %
Genes
34 %
Glanzmann's thrombasthenia.

By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders in Germany.

ITGB3, ITGA2B
Specificity
100 %
Genes
34 %
Alloimmune thrombocytopenia.

By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders in Germany.

ITGB3, ITGA2B
Specificity
100 %
Genes
34 %
Glanzmann's Thrombasthenia Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

ITGB3, ITGA2B
Specificity
100 %
Genes
34 %
Glanzmann's Thrombasthenia via the ITGB3 Gene.

By PreventionGenetics PreventionGenetics in United States.

ITGB3
Specificity
100 %
Genes
17 %
Thrombocytopenia NGS Panel.

By Connective Tissue Gene Tests in United States.

RUNX1, SMPD1, CYCS, AP3B1, ANKRD26, GBA, MPL, WAS, MYH9, GATA1, LYST, ADAMTS13, TBXAS1, NBEAL2, HOXA11, ITGB3, ITGA2B, MASTL, ETV6, RBM8A , (...)

View the complete list with 8 more genes
Specificity
8 %
Genes
34 %
Thrombocytopenia Deletion / Duplication Panel.

By Connective Tissue Gene Tests in United States.

RUNX1, SMPD1, CYCS, AP3B1, ANKRD26, GBA, MPL, WAS, MYH9, GATA1, LYST, ADAMTS13, TBXAS1, NBEAL2, HOXA11, ITGB3, ITGA2B, MASTL, ETV6, RBM8A , (...)

View the complete list with 8 more genes
Specificity
8 %
Genes
34 %
Thrombocytopenia Comprehensive Panel.

By Connective Tissue Gene Tests in United States.

RUNX1, SMPD1, CYCS, AP3B1, ANKRD26, GBA, MPL, WAS, MYH9, GATA1, LYST, ADAMTS13, TBXAS1, NBEAL2, HOXA11, ITGB3, ITGA2B, MASTL, ETV6, RBM8A , (...)

View the complete list with 8 more genes
Specificity
8 %
Genes
34 %
Thrombocytopenia, neonatal alloimmune.

By Centogene AG - the Rare Disease Company in Germany.

ITGB3
Specificity
100 %
Genes
17 %
Glanzmann Thrombasthenia (ITGA2B & ITGB3).

By Molecular Haemostasis & Thrombosis GSTS Pathology - Guy's and St. Thomas' NHS Foundation Trust in United Kingdom.

ITGB3, ITGA2B
Specificity
100 %
Genes
34 %
Glanzmann thrombasthenia.

By Medical Genetics Laboratory Diagenom GmbH in Germany.

ITGB3, ITGA2B
Specificity
100 %
Genes
34 %
Thrombasthenia (Glanzmann and Naegli).

By Praxis fuer Humangenetik Wien in Austria.

ITGB3
Specificity
100 %
Genes
17 %
Glanzmann Thrombasthenia ITGB3.

By Regional Molecular Haemostasis Laboratory Birmingham Childrens Hospital NHS Foundation Trust in United Kingdom.

ITGB3
Specificity
100 %
Genes
17 %
Thrombasthenia (Glanzmann and Naegli).

By MedGene in Slovakia.

ITGB3
Specificity
100 %
Genes
17 %
ITGB3.

By Fulgent Genetics Fulgent Genetics in United States.

ITGB3
Specificity
100 %
Genes
17 %
Glanzmann thrombasthenia.

By Bioarray in Spain.

ITGB3
Specificity
100 %
Genes
17 %
GLANZMANN THROMBASTHENIA.

By Laboratorio de Genetica Clinica SL in Spain.

ITGB3, ITGA2B
Specificity
100 %
Genes
34 %
Glanzmann Thrombasthenia , Sequencing ITGB3 Gene.

By Reference Laboratory Genetics in Spain.

ITGB3
Specificity
100 %
Genes
17 %
Thrombasthenia of Glanzmann , Panel Massive Sequencing (NGS) ITGA2B,ITGB3 Genes.

By Reference Laboratory Genetics in Spain.

ITGB3, ITGA2B
Specificity
100 %
Genes
34 %
ITGA2B. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

ITGA2B
Specificity
100 %
Genes
17 %
Glanzmann thrombasthenia (sequence analysis of ITGA2B gene).

By CGC Genetics in Portugal.

ITGA2B
Specificity
100 %
Genes
17 %
Glanzmann's Thrombasthenia via the ITGA2B Gene.

By PreventionGenetics PreventionGenetics in United States.

ITGA2B
Specificity
100 %
Genes
17 %
Thrombocytopenia, neonatal alloimmune.

By Centogene AG - the Rare Disease Company in Germany.

ITGA2B
Specificity
100 %
Genes
17 %
Glanzmann Thrombasthenia ITGA2B.

By Regional Molecular Haemostasis Laboratory Birmingham Childrens Hospital NHS Foundation Trust in United Kingdom.

ITGA2B
Specificity
100 %
Genes
17 %
ITGA2B.

By Fulgent Genetics Fulgent Genetics in United States.

ITGA2B
Specificity
100 %
Genes
17 %
Glanzmann thrombasthenia.

By Bioarray in Spain.

ITGA2B
Specificity
100 %
Genes
17 %
Glanzmann Thrombasthenia , Sequencing ITGA2B Gene.

By Reference Laboratory Genetics in Spain.

ITGA2B
Specificity
100 %
Genes
17 %
Bernard Soulier syndrome Type B.

By Genetics Laboratory University of Oklahoma Health Sciences Center in United States.

GP1BB
Specificity
100 %
Genes
17 %
GP1BB Deletion/duplication analysis.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

GP1BB
Specificity
100 %
Genes
17 %
GP1BB Sequencing.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

GP1BB
Specificity
100 %
Genes
17 %
GPIbß sequencing.

By Genetic Services Laboratory University of Chicago in United States.

GP1BB
Specificity
100 %
Genes
17 %
GPIbß deletion/duplication analysis.

By Genetic Services Laboratory University of Chicago in United States.

GP1BB
Specificity
100 %
Genes
17 %
GP1BB. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

GP1BB
Specificity
100 %
Genes
17 %
Bernard-Soulier syndrome (sequence analysis of GP1BB gene).

By CGC Genetics in Portugal.

GP1BB
Specificity
100 %
Genes
17 %
Bernard-Soulier Syndrome Type B.

By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders in Germany.

GP1BB
Specificity
100 %
Genes
17 %
Bernard-Soulier Syndrome via GP1BB Gene Sequencing with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

GP1BB
Specificity
100 %
Genes
17 %
Bernard Soulier syndrome type B.

By Centogene AG - the Rare Disease Company in Germany.

GP1BB
Specificity
100 %
Genes
17 %
Bernard-Soulier syndrome B.

By Praxis fuer Humangenetik Wien in Austria.

GP1BB
Specificity
100 %
Genes
17 %
Bernard-Soulier Syndrome Type B.

By Regional Molecular Haemostasis Laboratory Birmingham Childrens Hospital NHS Foundation Trust in United Kingdom.

GP1BB
Specificity
100 %
Genes
17 %
Bernard-Soulier syndrome B.

By MedGene in Slovakia.

GP1BB
Specificity
100 %
Genes
17 %
Pan-Ethnic Carrier Screen: Gene Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

FMR1, HFE, ACADM, ACADS, AGL, ACADVL, ACAT1, ALDOB, ALPL, BTD, ATP7B, BCKDHA, BCKDHB, BCS1L, GAA, HBB, MMACHC, CHM, TYR, SLC37A4 , (...)

View the complete list with 127 more genes
Specificity
1 %
Genes
17 %
GP1BB.

By Fulgent Genetics Fulgent Genetics in United States.

GP1BB
Specificity
100 %
Genes
17 %
Bernard-Soulier Syndrome Type B , Sequencing GP1BB Gene.

By Reference Laboratory Genetics in Spain.

GP1BB
Specificity
100 %
Genes
17 %
Pan-Ethnic Carrier Screen: Full Gene Sequencing and SMA Analysis.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

HFE, ACADM, ACADS, AGL, ACADVL, ACAT1, ALDOB, ALPL, BTD, ATP7B, BCKDHA, BCKDHB, BCS1L, GAA, HBB, MMACHC, TYR, SLC37A4, HSD17B4, CPT2 , (...)

View the complete list with 116 more genes
Specificity
1 %
Genes
17 %

Alternate names

Integrin, Beta-3; Itgb3 Is also known as platelet glycoprotein iiia;gp3a, gp iiia, platelet fibrinogen receptor, beta subunit, cd61;nait.



If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like PRECOCIOUS PUBERTY, CENTRAL, 2; CPPB2 MYASTHENIC SYNDROME, CONGENITAL, 19; CMS19

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