RPGRIP1

RPGR interacting protein 1
OMIM: 605446, ClinGen, DECIPHER

9 panels

Panel Reviews Mode of inheritance Details
9 panels

Green RPGRIP1 in Ciliopathies


Level 2: Dysmorphic and congenital abnormality syndromes
Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert Review
Phenotypes
  • Leber congenital amaurosis 6 (MIM#613826)

Green RPGRIP1 in Mendeliome


Version 2.0

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert Review
  • Victorian Clinical Genetics Services
Phenotypes
  • Cone-rod dystrophy 13 (MIM#608194) , Leber congenital amaurosis (MIM#61382)

Red RPGRIP1 in Skeletal dysplasia

Level 3: Skeletal dysplasias
Level 2: Skeletal disorders
Version 1.0

2 reviews Not set
Sources
  • Expert Review
  • Emory Genetics Laboratory

Green RPGRIP1 in Retinitis pigmentosa


Level 2: Ophthalmological disorders
Version 1.0

0 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Royal Melbourne Hospital
Phenotypes
  • Leber congenital amaurosis 6, 613826
  • Cone-rod dystrophy 13, 608194

Green RPGRIP1 in Macular Dystrophy/Stargardt Disease


Level 2: Ophthalmological disorders
Version 1.0

0 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Royal Melbourne Hospital
  • Expert Review Green
Phenotypes
  • Leber congenital amaurosis 6, 613826
  • Cone-rod dystrophy 13, 608194

Green RPGRIP1 in Mackenzie's Mission_Reproductive Carrier Screening


Level 2: Screening
Version 1.0

0 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Mackenzie's Mission
Phenotypes
  • Cone-rod dystrophy 13, 608194 (3)

Green RPGRIP1 in Cone-rod Dystrophy


Level 2: Ophthalmological disorders
Version 1.0

0 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Royal Melbourne Hospital
Phenotypes
  • Cone-rod dystrophy 13, 608194

Green RPGRIP1 in Congenital nystagmus


Level 2: Ophthalmological disorders
Version 2.0

3 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert list
  • Expert Review
Phenotypes
  • Leber congenital amaurosis 6, MIM# 613826
  • congenital nystagmus

Green RPGRIP1 in Prepair 1000+


Level 2: Screening
Version 3.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Mackenzie's Mission
Phenotypes
  • Cone-rod dystrophy 13 MIM#608194, MONDO:0011987, Leber congenital amaurosis MIM#61382,MONDO:0013446