protein-coupled receptor 98 (GPR98) or Very Large G-protein coupled receptor 1 (VLGR1), is a protein that in humans is encoded by the GPR98 gene. Several alternatively...
11 KB (1,126 words) - 12:44, 4 September 2024
type II may be caused by mutations in any of three different genes: USH2A, GPR98 and DFNB31. The protein encoded by the USH2A gene, usherin, is located in...
34 KB (3,528 words) - 20:30, 29 October 2024
worldwide SMPD1 Usher syndrome 1:23000 in the U.S. 1:28000 in Norway 1:12500 in Germany CDH23, CLRN1, DFNB31, GPR98, MYO7A, PCDH15, USH1C, USH1G, USH2A...
99 KB (10,142 words) - 15:38, 13 October 2024
Genetic associations Type OMIM Gene FEB3A 604403 SCN1A FEB3B 604403 SCN9A FEB4 604352 GPR98 FEB8 611277 GABRG2...
29 KB (2,998 words) - 19:30, 16 March 2024
female births Usher syndrome MYO7A, USH1C, CDH23, PCDH15, USH1G, USH2A, GPR98, DFNB31, CLRN1 recessive 3-6:100,000 (type I) Variegate porphyria PPOX dominant...
42 KB (983 words) - 18:14, 6 October 2024
infantile, 3; 607745; SCN2A1 Convulsions, familial febrile, 4; 604352; GPR98 COPD, rate of decline of lung function in; 606963; MMP1 Coproporphyria;...
234 KB (18,877 words) - 15:43, 9 May 2024