Genes in panel

Fetal anomalies

Gene: TP53RK

Green List (high evidence)

TP53RK (TP53 regulating kinase)
EnsemblGeneIds (GRCh38): ENSG00000172315
EnsemblGeneIds (GRCh37): ENSG00000172315
OMIM: 608679, Gene2Phenotype
TP53RK is in 4 panels

2 reviews

Arina Puzriakova (Genomics England Curator)

Green List (high evidence)

The rating of this gene has been updated to Green and the mode of inheritance set to BIALLELIC, autosomal or pseudoautosomal following NHS Genomic Medicine Service approval.
Created: 10 Mar 2026, 12:27 p.m. | Last Modified: 10 Mar 2026, 12:27 p.m.
Panel Version: 6.149
This gene and phenotype were reviewed during meetings between November 2025 & January 2026. The meetings included representatives of the Central & South and North Thames R21 testing GLHs and from the R21 Clinical Oversight Group. Clinical review and curation was performed by Stephanie Allen, Elizabeth Young and Sarah Graham (Central & South GLH), Natalie Chandler and Elizabeth Scotchman (North Thames GLH), and Tazeen Ashraf, Anna De Burca, Natalie Canham, Samantha Doyle, Alice Gardham, Victoria Harrison, Tessa Homfray, Esther Kinning, and Soo-Mi Park (R21 Clinical Oversight Group).
Created: 10 Mar 2026, 11:35 a.m. | Last Modified: 10 Mar 2026, 11:35 a.m.
Panel Version: 6.148

Natalie Canham (Liverpool Women's Hospital)

Green List (high evidence)

associated with distal arthrogryposis picture, thin CC, Dandy Walker. Plenty of evidence
Created: 10 Mar 2026, 11:27 a.m. | Last Modified: 10 Mar 2026, 11:27 a.m.
Panel Version: 6.147

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
Galloway-Mowat syndrome 4, OMIM:617730

Publications

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
Phenotypes
  • Galloway-Mowat syndrome 4, OMIM:617730
OMIM
608679
Clinvar variants
Variants in TP53RK
Penetrance
None
Panels with this gene

History Filter Activity

10 Mar 2026, Gel status: 3

Set Phenotypes

Arina Puzriakova (Genomics England Curator)

Added phenotypes Galloway-Mowat syndrome 4, OMIM:617730 for gene: TP53RK

9 Mar 2026, Gel status: 3

Created, Added New Source, Set mode of inheritance

Arina Puzriakova (Genomics England Curator)

gene: TP53RK was added gene: TP53RK was added to Fetal anomalies. Sources: Expert Review Green Mode of inheritance for gene: TP53RK was set to BIALLELIC, autosomal or pseudoautosomal