GPR179

G protein-coupled receptor 179
OMIM: 614515, Gene2Phenotype

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green GPR179 in Mendeliome Version 1.1902	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Night blindness, congenital stationary (complete), 1E, autosomal recessive (MIM#614565)
Green GPR179 in Congenital Stationary Night Blindness Level 2: Ophthalmological disorders Version 0.23 Component of the following Super Panels: Retinal Disorders Superpanel	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Royal Melbourne Hospital Phenotypes Night blindness, congenital stationary (complete), 1E, autosomal recessive, 614565
Green GPR179 in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.109	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Night blindness, congenital stationary (complete), 1E, autosomal recessive, 614565 (3)
Green GPR179 in Congenital nystagmus Level 2: Ophthalmological disorders Version 1.21	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Royal Melbourne Hospital Phenotypes Night blindness, congenital stationary (complete), 1E, autosomal recessive, 614565
Green GPR179 in Prepair 1000+ Level 2: Screening Version 1.9	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Night blindness, congenital stationary (complete), 1E, autosomal recessive, 614565 (3)