Genomics England
GMS Panels
Panels
Genes and Entities

IFT27

intraflagellar transport 27
OMIM: 615870
PanelMode of inheritanceDetails
6 panels
Green
in Bardet Biedl syndrome
R-numbers: R107
Signed-off version 2.16
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Bardet-Biedl syndrome 19, OMIM:615996
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 7.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Bardet-Biedl syndrome 19, OMIM:615996
Green
in Limb disorders
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 8.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Bardet-Biedl syndrome 19, OMIM:615996, Polydactyly
Green
in Ophthalmological ciliopathies
Component of the following Super Panels:
  • - Paediatric disorders
  • - Rare multisystem ciliopathy Super panel
Signed-off version 6.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Bardet-Biedl syndrome 19, OMIM:615996
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 5.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Bardet-Biedl syndrome 19, OMIM:615996
Green
in Retinal disorders
R-numbers: R32
Signed-off version 9.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Bardet-Biedl syndrome 19, OMIM:615996