NR2E3

nuclear receptor subfamily 2 group E member 3
OMIM: 604485, ClinGen, DECIPHER

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green NR2E3 in Mendeliome Version 1.2302	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Retinitis pigmentosa 37 - MIM#611131 Enhanced S-cone syndrome - MIM#268100 Goldmann-Favre syndrome - MONDO#0100289 retinal dystrophy
Green NR2E3 in Retinitis pigmentosa_Autosomal Recessive/X-linked Level 2: Ophthalmological disorders Version 0.155 Component of the following Super Panels: Retinal Disorders Superpanel Retinitis Pigmentosa Superpanel	0 reviews	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Royal Melbourne Hospital Phenotypes Enhanced S - cone syndrome (AR) Retinitis pigmentosa 37 (AD and AR)
Green NR2E3 in Retinitis pigmentosa_Autosomal Dominant Level 2: Ophthalmological disorders Version 0.57 Component of the following Super Panels: Retinal Disorders Superpanel Retinitis Pigmentosa Superpanel	0 reviews	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Royal Melbourne Hospital Phenotypes Enhanced S - cone syndrome (AR) Retinitis pigmentosa 37 (AD and AR)
Green NR2E3 in Vitreoretinopathy Level 2: Ophthalmological disorders Version 1.5 Component of the following Super Panels: Retinal Disorders Superpanel	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Enhanced S-cone syndrome, MIM# 268100
Red NR2E3 in Prepair 1000+ Level 2: Screening Version 1.1566	2 reviews	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Enhanced S-cone syndrome (MIM#268100) Retinitis pigmentosa 37 (MIM#611131)