Disorders


 

Crohn Disease


 

OMIM

GeneLocusProtein
NOD216q12Nucleotide-binding oligomerization domain-containing protein 2

Laboratory Test Method Prenatal Carrier *
bio.logis Center for Human Genetics - Frankfurt, Germany• Sequence analysis of select exons
  
Center for Genetics at Saint Francis, Genetics Laboratory - Tulsa, OK, USA• Sequence analysis of the entire coding region
Center for Human Genetics and Laboratory Medicine Martinsried, Molecular Genetics - Martinsried, Germany• Sequence analysis of select exons
• Targeted mutation analysis
Center for Human Genetics, Bioscientia GmbH - Ingelheim, Germany• Targeted mutation analysis
CGB Laboratory Inc - Ostrava, Czech Republic• Targeted mutation analysis
CGC Genetics - Porto, Portugal• Targeted mutation analysis
CHRU Montpellier, Laboratoire des maladies rares et Auto-Inflammatoires - Montpellier, France• Targeted mutation analysis
• Mutation scanning of select exons
Dr. Eberhard and Partner, MVZ Dortmund - Dortmund, Germany• Sequence analysis of the entire coding region
• Sequence analysis of select exons
GENETAQ, Molecular Genetics Centre - Malaga, Spain• Sequence analysis of the entire coding region
• Targeted mutation analysis
GGA - Galil Genetic Analysis - Kazerin, Israel• Sequence analysis of the entire coding region
 
MGZ München, Medizinisch Genetisches Zentrum Mnchen - München, Germany• Targeted mutation analysis
 
Pronto Diagnostics Ltd., ProntoLab - MLPA Lab - Tel Aviv, Israel• Sequence analysis of the entire coding region
Tor Vergata University of Roma, School of Medicine, Servizio di Genetica Medica - Rome, Italy• Mutation scanning of the entire coding region

* 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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