GPR179

G protein-coupled receptor 179
OMIM: 614515, ClinGen, DECIPHER

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green GPR179 in Mendeliome Version 1.2302	1 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	1 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	0 reviews	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 1.22	2 reviews	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 1.1566	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes Night blindness, congenital stationary (complete), 1E, autosomal recessive, 614565 (3)