Disorders


 

KCNJ11-Related Hyperinsulinism


 

OMIM

GeneLocusProtein
KCNJ1111p15.1ATP-sensitive inward rectifier potassium channel 11

Laboratory Test Method Prenatal Carrier *
Academic Medical Centre, University of Amsterdam, DNA Diagnostics Laboratory - Amsterdam, Netherlands  
Ambry Genetics Corp, Ambry Genetics - Aliso Viejo, CA, USA  
Athena Diagnostics Inc, Reference Lab - Worcester, MA, USA  
bio.logis Center for Human Genetics - Frankfurt, Germany  
Center for Human Genetics, Bioscientia GmbH - Ingelheim, Germany  
Center for Nephrology and Metabolic Disorders, Laboratory for Molecular Diagnostics - Weisswasser, Germany  
Centogene AG, Rare Disease Company - Rostock, Germany  
GENETAQ, Molecular Genetics Centre - Malaga, Spain  
Hadassah-Hebrew University Medical Center, Endocrinology and Metabolism Service - Jerusalem, Israel  
Klinikum Stuttgart, Institute of Clinical Genetics - Stuttgart, Germany  
Laboratory for Molecular Diagnostics, Labor-MVZ Westmecklenburg - Schwerin, Germany  
Odense University Hospital, Department of Genetics - Odense, Denmark  
Royal Devon and Exeter Hospital, Department of Molecular Genetics - Exeter, Great Britain• Sequence analysis of select exons
  
Seattle Children's Hospital, Biochemical and Molecular Genetics Laboratories - Seattle, WA, USA  
Synlab MVZ Humane Genetik Mnchen, Labor fr Humangenetik - München, Germany  
University of Chicago, Genetic Services Laboratory - Chicago, IL, 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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