Health Conditions Related to Genetic Changes
Bradyopsia
At least two mutations in the RGS9 gene have been found to cause bradyopsia, a rare condition that affects vision. In people with bradyopsia, the eyes adapt more slowly than usual to changing light conditions (for example, walking out of a darkened movie theater into daylight or driving into a dark tunnel on a sunny day). Some affected individuals also have difficulty seeing small moving objects, such as a tennis ball.
The RGS9 gene mutations that cause bradyopsia greatly reduce or eliminate the function of RGS9-1 in photoreceptors. (These mutations do not appear to affect the function of RGS9-2 in the brain.) A loss of RGS9-1 function prevents photoreceptors from recovering quickly after responding to light. Normally they return to their resting state in a fraction of a second, but in people with RGS9 gene mutations, it can take ten seconds or longer. During that time, the photoreceptors cannot respond to light. This delay causes temporary blindness in response to changing light conditions and may interfere with seeing small objects when they are in motion.
More About This Health ConditionOther Names for This Gene
- MGC111763
- MGC26458
- regulator of G-protein signaling 9
- regulator of G-protein signalling 9
- RGS9L
Additional Information & Resources
Tests Listed in the Genetic Testing Registry
Scientific Articles on PubMed
Catalog of Genes and Diseases from OMIM
References
- Martemyanov KA, Arshavsky VY. Biology and functions of the RGS9 isoforms. Prog Mol Biol Transl Sci. 2009;86:205-27. doi: 10.1016/S1877-1173(09)86007-9. Epub 2009 Oct 7. Citation on PubMed
- Michaelides M, Li Z, Rana NA, Richardson EC, Hykin PG, Moore AT, Holder GE, Webster AR. Novel mutations and electrophysiologic findings in RGS9- and R9AP-associated retinal dysfunction (Bradyopsia). Ophthalmology. 2010 Jan;117(1):120-127.e1. doi: 10.1016/j.ophtha.2009.06.011. Epub 2009 Oct 8. Citation on PubMed
- Nishiguchi KM, Sandberg MA, Kooijman AC, Martemyanov KA, Pott JW, Hagstrom SA, Arshavsky VY, Berson EL, Dryja TP. Defects in RGS9 or its anchor protein R9AP in patients with slow photoreceptor deactivation. Nature. 2004 Jan 1;427(6969):75-8. doi: 10.1038/nature02170. Citation on PubMed
- Psifogeorgou K, Papakosta P, Russo SJ, Neve RL, Kardassis D, Gold SJ, Zachariou V. RGS9-2 is a negative modulator of mu-opioid receptor function. J Neurochem. 2007 Oct;103(2):617-25. doi: 10.1111/j.1471-4159.2007.04812.x. Epub 2007 Aug 23. Citation on PubMed
The information on this site should not be used as a substitute for professional medical care or advice. Contact a health care provider if you have questions about your health.