Disorders

Congenital Stationary Night Blindness, Autosomal Dominant 3

Synonym(s): Autosomal Dominant Congenital Stationary Night Blindness, Nougaret Type, CSNBAD3, GNAT1-Related Autosomal Dominant Congenital Stationary Night Blindness

OMIM

Gene	Locus	Protein
GNAT1	3p21	Guanine nucleotide-binding protein G(t) subunit alpha-1

Laboratory	Test Method	Prenatal	Carrier *
CeGaT GmbH - Tuebingen, Germany
Centogene AG, Rare Disease Company - Rostock, Germany
GeneDx - Gaithersburg, MD, USA
Oregon Health and Science University, Casey Eye Institute Molecular Diagnostic Laboratory - Portland, OR, 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.