Osteogenesis imperfecta
Gene: RAF1EnsemblGeneIds (GRCh38): ENSG00000132155
EnsemblGeneIds (GRCh37): ENSG00000132155
OMIM: 164760, Gene2Phenotype
RAF1 is in 19 panels
2 reviews
Rebecca Pollitt (Sheffield Diagnostic Genetics Service ; University of Sheffield)
Meena Balasubramanian (Sheffield Children's NHS Foundation Trust)
Remove from panelCreated: 27 Nov 2015, 3:04 p.m.
Details
- Sources
-
- Expert Review Removed
- Emory Genetics Laboratory
- Phenotypes
-
- Proportionate Short Stature/Small for Gestational Age
- Tags
- OMIM
- 164760
- Clinvar variants
- Variants in RAF1
- Penetrance
- Complete
- Panels with this gene
-
- Paediatric or syndromic cardiomyopathy
- Childhood solid tumours cancer susceptibility
- Primary lymphoedema
- Hypertrophic cardiomyopathy
- Hereditary neuropathy or pain disorder
- Adult solid tumours cancer susceptibility
- Monogenic short stature
- Fetal anomalies
- Osteogenesis imperfecta
- Dilated Cardiomyopathy and conduction defects
- Pigmentary skin disorders
- Fetal hydrops
- Neurofibromatosis Type 1
- Hereditary neuropathy
- DDG2P
- RASopathies
- IUGR and IGF abnormalities
- Childhood solid tumours
- Intellectual disability
History Filter Activity
Added Tag
Arina Puzriakova (Genomics England Curator)Tag curated_removed tag was added to gene: RAF1.
Gene classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)This gene has been removed from the panel.
Added New Source
Ellen McDonagh (Genomics England Curator)RAF1 was added to Osteogenesis Imperfecta panel. Sources: Emory Genetics Laboratory