IFITM5

interferon induced transmembrane protein 5
OMIM: 614757
PanelMode of inheritanceDetails
4 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
OSTEOGENESIS IMPERFECTA TYPE V 610967
R-numbers: R21
Signed-off version 1.92
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
OSTEOGENESIS IMPERFECTA TYPE V
R-numbers: R102
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Osteogenesis imperfecta, type V, 610967, Osteogenesis Imperfecta and Decreased Bone Density, skeletal dysplasias, c-14C>T IFITM5 testing
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R104
Signed-off version 2.2
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Osteogenesis imperfecta, type V 610967