Disorders

Polycystic Kidney Disease 1, Autosomal Dominant

Synonym(s): PKD 1

Gene	Locus	Protein
PKD1	16p13.3	Polycystin-1

Laboratory	Test Method	Prenatal	Carrier *
Aachen, RWTH, Institute of Human Genetics - Aachen, Germany	• Linkage analysis
Athena Diagnostics Inc, Reference Lab - Worcester, MA, USA
Center for Genetics at Saint Francis, Genetics Laboratory - Tulsa, OK, USA	• Linkage analysis
Center for Human Genetics and Laboratory Medicine Martinsried, Molecular Genetics - Martinsried, Germany
Centogene AG, Rare Disease Company - Rostock, Germany
CGC Genetics - Porto, Portugal
Cyprus Institute of Neurology and Genetics, Molecular Genetics, Function and Therapy - Nicosia, Cyprus	• Linkage analysis
Diagenom GmbH, Medical Genetics Laboratory - Rostock, Germany
GENDA - Ciudad autonoma de Buenos Aires, Argentina	• Linkage analysis
GENETAQ, Molecular Genetics Centre - Malaga, Spain
GGA - Galil Genetic Analysis - Kazerin, Israel
Innovagenomics S.L, Innovagenomics - Salamanca, Spain	• Sequence analysis of select exons
Klinikum Stuttgart, Institute of Clinical Genetics - Stuttgart, Germany
Laboratory for Molecular Diagnostics, Labor-MVZ Westmecklenburg - Schwerin, Germany
Sheffield Children's NHS Foundation Trust, Sheffield Diagnostic Genetics Service - Sheffield, Great Britain
Synlab MVZ Humane Genetik Mnchen, Labor fr Humangenetik - München, Germany
Tor Vergata University of Roma, School of Medicine, Servizio di Genetica Medica - Rome, Italy	• Linkage analysis

^* 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.