Genomics England
GMS Panels
Panels
Genes and Entities

RBP4

retinol binding protein 4
OMIM: 180250
PanelMode of inheritanceDetails
3 panels
Green
in Likely inborn error of metabolism - targeted testing not possible
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
  • - Unexplained death in infancy and sudden unexplained death in childhood
R-numbers: R98
Signed-off version 4.78
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Retinol binding protein deficiency (Other disorders of vitamins and cofactors), Posterior segment abnormalities
Green
in Retinal disorders
R-numbers: R32
Signed-off version 4.42
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Achromatopsia, Cone, and Cone-rod Dystrophy, Macular Dystrophy/Degeneration/Stargardt Disease, Congenital Stationary Night Blindness, Retinitis pigmentosa
Green
in Structural eye disease
R-numbers: R36
Signed-off version 3.0
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
Retinal dystrophy, iris coloboma, and comedogenic acne syndrome, 615147