Disorders


 

MSH2-Related Lynch Syndrome


Synonym(s): MSH2-Related Hereditary Non-Polyposis Colon Cancer, MSH2-Related HNPCC

 

OMIM

GeneLocusProtein
MSH22p21DNA mismatch repair protein Msh2

Laboratory Test Method Prenatal Carrier *
Aarhus University Hospital, Department of Molecular Medicine - Aarhus, Denmark• Sequence analysis of select exons
• Mutation scanning of select exons
  
Academic Medical Centre, University of Amsterdam, DNA Diagnostics Laboratory - Amsterdam, Netherlands  
Addenbrooke's Hospital, Molecular Genetics Laboratory - Cambridge, Great Britain  
Ambry Genetics Corp, Ambry Genetics - Aliso Viejo, CA, USA• Immunohistochemistry
  
Amplexa Genetics A/S, Amplexa Genetics - Odense, Denmark  
ARUP Laboratories, Molecular Genetics Laboratory - Salt Lake City, UT, USA• Immunohistochemistry
  
Asper Biotech Ltd., Asper Biotech - Tartu, Estonia  
Baylor College of Medicine, Medical Genetics Laboratories - Houston, TX, USA• Immunohistochemistry
  
Center for Human Genetics, Bioscientia GmbH - Ingelheim, Germany  
Center for Human Genetics, Inc - Cambridge, MA, USA  
Centogene AG, Rare Disease Company - Rostock, Germany  
CGC Genetics - Porto, Portugal  
Children's Hospital of Eastern Ontario, Molecular Genetics Diagnostic Laboratory - Ottawa, Canada  
City of Hope National Medical Center, Clinical Molecular Diagnostic Laboratory - Duarte, CA, USA• Immunohistochemistry
  
Diagenom GmbH, Medical Genetics Laboratory - Rostock, Germany  
Dr. Eberhard and Partner, MVZ Dortmund - Dortmund, Germany  
Emory University School of Medicine, Emory Molecular Genetics Laboratory - Atlanta, GA, USA• Immunohistochemistry
  
Endokrinologikum Hamburg - Center for Hormonal and Metabolic Diseases, Prenatal, and Reproductive Medicine, Molecular Diagnostics - Hamburg, Germany  
GGA - Galil Genetic Analysis - Kazerin, Israel  
Harvard Medical School and Partners Healthcare, Laboratory for Molecular Medicine - Cambridge, MA, USA  
Hospital Italiano de Buenos Aires, ICBME - Unidad de Medicina Molecular y Genómica - Buenos Aires, Argentina• Mutation scanning of the entire coding region
• Immunohistochemistry
  
Huntington Medical Research Institutes, Cancer Genetics Laboratory - Pasadena, CA, USA• Immunohistochemistry
  
HUSLAB, Laboratory of Genetics - Helsinki, Finland  
Innovagenomics S.L, Innovagenomics - Salamanca, Spain  
Institut de Cancrologie Gustave Roussy, Laboratoire de Gntique - Villejuif, France  
Institute of Medical Genetics, All Wales Molecular Genetics Laboratory - Cardiff, Great Britain  
Instituto de Medicina Genmica, IMEGEN - Paterna, Spain  
InVitae Corporation - San Francisco, CA, USA  
Klinikum Stuttgart, Institute of Clinical Genetics - Stuttgart, Germany  
LabPLUS - Auckland City Hospital, Molecular Genetics Laboratory - Diagnostics Genetics - Auckland, New Zealand  
London Health Sciences Centre, Molecular Diagnostic Laboratory - London, Canada• Immunohistochemistry
  
Maastricht University Medical Centre, Clinical Genomics - Maastricht, Netherlands  
Masaryk Memorial Cancer Institute, Cancer Epidemiology and Genetics - Brno, Czech Republic• Sequence analysis of select exons
• Mutation scanning of the entire coding region
  
Mayo Clinic - Minnesota, Molecular Genetics Laboratory - Rochester, MN, USA• Immunohistochemistry
  
Medgene, MedGene - Bratislava, Slovakia  
MGZ München, Medizinisch Genetisches Zentrum München - München, Germany• Immunohistochemistry
  
Mount Sinai Hospital, Advanced Molecular Diagnostics - Toronto, Canada  
Myriad Genetic Laboratories, Inc., Myriad Genetic Laboratories - Salt Lake City, UT, USA  
Northwick Park and St. Mark's Hospitals, Kennedy-Galton Centre - NW Thames Regional Genetics Service - Harrow, Great Britain• Immunohistochemistry
  
Oregon Health and Science University, Knight Diagnostic Laboratories - Molecular Diagnostic Center - Portland, OR, USA  
Oxford Medical Genetics Laboratories, Oxford Genetics Laboratories - Oxford, Great Britain  
Praxis fuer Humangenetik Wien - Vienna, Austria  
PreventionGenetics, Clinical DNA Testing and DNA Banking - Marshfield, WI, USA  
Pronto Diagnostics Ltd., ProntoLab - MLPA Lab - Tel Aviv, Israel• Targeted mutation analysis
  
Quest Diagnostics Nichols Institute - California, Molecular Genetics Laboratory - San Juan Capistrano, CA, USA  
Rabin Medical Center, Molecular Genetics - Petah Tikva, Israel• Targeted mutation analysis
  
Radboud University Nijmegen Medical Centre, Genome Diagnostics Nijmegen - Nijmegen, Netherlands  
Ruhr University, Human Genetics - Bochum, Germany  
Samsung Medical Center, Department of Laboratory Medicine and Genetics - Seoul, South Korea  
Seoul National University Hospital, Molecular Diagnostics Laboratory - Seoul, South Korea  
Shaare Zedek Medical Center, Medical Genetics Institute - Jerusalem, Israel• Targeted mutation analysis
  
Sheffield Children's NHS Foundation Trust, Sheffield Diagnostic Genetics Service - Sheffield, Great Britain  
Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain  
St. Elisabeth Cancer Institute, Department of Clinical Genetics - Heydukova 2, Slovakia  
Synlab MVZ Humane Genetik Mnchen, Labor fr Humangenetik - München, Germany  
University Children's Hospital, Labor Molekulargenetik, Abteilung Medizinische Genetik - Basel, Switzerland  
University Hospitals - University Hospitals Laboratory Service Foundation, Center for Human Genetics Laboratory - Cleveland, OH, USA  
University of Bonn, Institute of Human Genetics - Bonn, Germany  
University of Oklahoma Health Sciences Center, Genetics Laboratory - Oklahoma City, OK, USA  
University of Washington Medical Center, Laboratory Medicine-Genetics Laboratory - Seattle, WA, USA  

* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.

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