Genomics England
GMS Panels
Panels
Genes and Entities

ISCA-37432-Loss

17q12 recurrent (RCAD syndrome) region (includes HNF1B) Loss
PanelMode of inheritanceDetails
3 panels
Green
in Cystic kidney disease
Component of the following Super Panels:
  • - Cystic renal disease
  • - Unexplained young onset end-stage renal disease
Signed-off version 5.4
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
RCAD syndrome, utero-vaginal atresia, Schizophrenia, 614527, delayed development, intellectual disability, Renal cysts and diabetes syndrome, Autism Spectrum Disorder, Mayer-Rokitansky-Kster-Hauser (MRKH) syndrome in females, Chromosome 17q12 deletion syndrome, global developmental delay
Green
in Intellectual disability
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 6.13
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
RCAD syndrome, utero-vaginal atresia, Schizophrenia, 614527, delayed development, intellectual disability, Renal cysts and diabetes syndrome, Autism Spectrum Disorder, Mayer-Rokitansky-Kster-Hauser (MRKH) syndrome in females, Chromosome 17q12 deletion syndrome, global developmental delay
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 3.7
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Schizophrenia, Mayer-Rokitansky-Kster-Hauser (MRKH) syndrome in females, delayed development, intellectual disability, 614527, RCAD syndrome, utero-vaginal atresia, Chromosome 17q12 deletion syndrome, Autism Spectrum Disorder, global developmental delay, Renal cysts and diabetes syndrome