Genomics England
GMS Panels
Panels
Genes and Entities

TXNDC15

thioredoxin domain containing 15
PanelMode of inheritanceDetails
4 panels
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 8.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Meckel syndrome 14, OMIM:619879
Green
in Limb disorders
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 9.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Meckel syndrome 14, OMIM:619879
Green
in Neurological ciliopathies
Component of the following Super Panels:
  • - Hereditary ataxia and cerebellar anomalies, childhood onset
  • - Paediatric disorders
  • - Rare multisystem ciliopathy Super panel
Signed-off version 7.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Meckel syndrome 14, OMIM:619879
Green
in Renal ciliopathies
Component of the following Super Panels:
  • - Cystic renal disease
  • - Paediatric disorders
  • - Rare multisystem ciliopathy Super panel
  • - Unexplained young onset end-stage renal disease
Signed-off version 5.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Meckel syndrome 14, OMIM:619879