Skeletal ciliopathies

Gene: TOPORS

Red List (low evidence)

TOPORS (TOP1 binding arginine/serine rich protein)
EnsemblGeneIds (GRCh38): ENSG00000197579
EnsemblGeneIds (GRCh37): ENSG00000197579
OMIM: 609507, Gene2Phenotype
TOPORS is in 10 panels

1 review

Ida Ertmanska (Genomics England Curator)

Red List (low evidence)

Comment on list classification: There are 4 probands reported in literature with Joubert syndrome and the same homozygous missense variant in TOPORS (p.Pro10Gln). All 4 individuals are of Dominican ancestry. Hence, this is likely a founder allele, and the gene should be rated Red, until more evidence emerges for the association. A founder-efffect tag was added.
Created: 3 Nov 2026, 11:44 a.m. | Last Modified: 3 Nov 2026, 11:44 a.m.
Panel Version: 7.5
PMID: 40358237 Lob & Brown, 2025
Report of a 12-month-old Dominican boy with a Dandy-Walker malformation (DWM, anomaly of cerebellar development), trigeminal neuralgia, molar tooth sign, mesoaxial polydactyly of hands and feet, hypotonia, and developmental delay. He was diagnosed with OFDS VI / Joubert syndrome. He was homozygous for TOPORS: c.29 C>A, p.Pro10Gln.

PMID: 37227088 Strong et al., 2023
Report of a proband of Dominican ancestry with Joubert syndrome. Exome seq showed he was homozygous for the c.29C>A, p.(Pro10Gln) variant in TOPORS.

PMID: 34132027 Strong et al., 2021
Study described two unrelated Dominican probands with oral cavity malformations, dysmorphic features, postaxial polydactyly, multiple lingual hamartomas, and dysmorphic features. Molar tooth sign also seen in Patient 2 - indicative of Joubert syndrome. Both patients were found to be homozygous for an identical TOPORS missense variant, c.29 C>A; (p.Pro10Gln). NO haplotype analysis. Variant may represent a Dominican Republic founder allele. 31 hets and no homozygotes reported in gnomAD v4.1.2. (MAF = 0.0001000, Admixed American pop).

TOPORS is not yet associated with a recessive disease entity in OMIM (heterozygous TOPORS variants between residues 807-867 are known to cause Retinitis pigmentosa 31) - OMIM accessed 3rd Nov 2026.
Sources: Literature
Created: 3 Nov 2026, 11:41 a.m.

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Joubert syndrome, MONDO:0018772

Publications

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Literature
Phenotypes
  • Joubert syndrome, MONDO:0018772
Tags
founder-effect
OMIM
609507
Clinvar variants
Variants in TOPORS
Penetrance
None
Publications
Panels with this gene

History Filter Activity

3 Nov 2026, Gel status: 1

Created, Added New Source, Added Tag, Set mode of inheritance, Set publications, Set Phenotypes

Ida Ertmanska (Genomics England Curator)

gene: TOPORS was added gene: TOPORS was added to Skeletal ciliopathies. Sources: Literature founder-effect tags were added to gene: TOPORS. Mode of inheritance for gene: TOPORS was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: TOPORS were set to 34132027; 37227088; 40358237 Phenotypes for gene: TOPORS were set to Joubert syndrome, MONDO:0018772 Review for gene: TOPORS was set to RED