Genomics England
GMS Panels
Panels
Genes and Entities

WRN

Werner syndrome RecQ like helicase
OMIM: 604611
PanelMode of inheritanceDetails
4 panels
Green
in Bilateral congenital or childhood onset cataracts
R-numbers: R31
Signed-off version 8.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Werner syndrome
Green
in Childhood solid tumours
Signed-off version 5.11
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Werner Syndrome, Werner syndrome, 277700
Green
in Sarcoma of possible germline origin
R-numbers: R457
Signed-off version 1.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Werner syndrome, MONDO:0010196, Werner syndrome, OMIM:277700
Green
in Severe insulin resistance and lipodystrophy syndromes
R-numbers: R158
Signed-off version 5.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Werner syndrome, OMIM:277700