TOPORS

TOP1 binding arginine/serine rich protein, E3 ubiquitin ligase
OMIM: 609507, ClinGen, DECIPHER

7 panels

Panel Reviews Mode of inheritance Details
7 panels

Amber TOPORS in Ciliopathies


Level 2: Dysmorphic and congenital abnormality syndromes
Version 2.0

3 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Expert Review
Phenotypes
  • ciliopathy, MONDO:0005308, TOPORS-associated
  • postaxial polydactyly, MONDO:0020927, TOPORS-related
  • multiple lingual hamartomas

Amber TOPORS in Joubert syndrome and other neurological ciliopathies


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • Joubert syndrome, MONDO:0018772, TOPORS-related
Tags
  • founder

Green TOPORS in Mendeliome


Version 2.0

2 reviews BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert Review
  • Victorian Clinical Genetics Services
Phenotypes
  • Retinitis pigmentosa 31 (MIM#609923)
  • Ciliopathy, MONDO:0005308, TOPORS-associated, AR

Amber TOPORS in Polydactyly


Level 2: Dysmorphic and congenital abnormality syndromes
Version 1.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • MONDO:0005308
  • ciliopathy
  • postaxial polydactyly
  • multiple lingual hamartomas
  • dysmorphic features

Red TOPORS 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 TOPORS in Retinitis pigmentosa


Level 2: Ophthalmological disorders
Version 1.0

1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Royal Melbourne Hospital
  • Expert Review Green
Phenotypes
  • Retinitis pigmentosa 31, MIM#609923
  • TOPORS-related retinopathy MONDO:0700233

Amber TOPORS in Fetal anomalies


Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Literature
Phenotypes
  • MONDO:0005308
  • ciliopathy
  • postaxial polydactyly
  • multiple lingual hamartomas
  • dysmorphic features