Cytopenias and congenital anaemias
Gene: SAMD9
SAMD9 (sterile alpha motif domain containing 9)
EnsemblGeneIds (GRCh38): ENSG00000205413
EnsemblGeneIds (GRCh37): ENSG00000205413
OMIM: 610456, Gene2Phenotype
SAMD9 is in 20 panels
EnsemblGeneIds (GRCh38): ENSG00000205413
EnsemblGeneIds (GRCh37): ENSG00000205413
OMIM: 610456, Gene2Phenotype
SAMD9 is in 20 panels
1 review
Helen Brittain (Genomics England Curator)
Comment when marking as ready: De novo missense to date. Sufficient cases with appropriate phenotype.Created: 15 May 2017, 8:54 a.m.
Sufficient cases for causation. De novo missense reported to date. Early anaemia and thrombocytopaenia a recurrent feature in the described cases. Therefore appropriate to include on this panel.Created: 15 May 2017, 8:47 a.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
MIRAGE syndrome, 617053
Publications
Mode of pathogenicity
Other
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
- Sources
-
- Expert Review Green
- Literature
- Phenotypes
-
- MIRAGE syndrome, 617053
- Tags
- OMIM
- 610456
- Clinvar variants
- Variants in SAMD9
- Penetrance
- Complete
- Publications
- Mode of Pathogenicity
- Other - please provide details in the comments
- Panels with this gene
-
- Gastrointestinal epithelial barrier disorders
- Monogenic short stature
- Infantile enterocolitis & monogenic inflammatory bowel disease
- Cytopenia - NOT Fanconi anaemia
- Radial dysplasia
- Intellectual disability
- Pigmentary skin disorders
- Cytopenias and congenital anaemias
- COVID-19 research
- Congenital adrenal hypoplasia
- Gastrointestinal neuromuscular disorders
- Fetal anomalies
- Familial Hirschsprung Disease
- Familial tumoral calcinosis
- Differences in sex development
- Primary immunodeficiency or monogenic inflammatory bowel disease
- IUGR and IGF abnormalities
- Inherited predisposition to acute myeloid leukaemia (AML)
- Multiple monogenic benign skin tumours
- DDG2P
History Filter Activity
15 May 2017, Gel status: 4
Gene classified by Genomics England curator
Helen Brittain (Genomics England Curator)This gene has been classified as Green List (High Evidence).
15 May 2017, Gel status: 4
Gene classified by Genomics England curator
Helen Brittain (Genomics England Curator)This gene has been classified as Green List (High Evidence).
15 May 2017, Gel status: 0
Added New Source
Helen Brittain (Genomics England Curator)SAMD9 was added to Cytopaenias and congenital anaemiaspanel. Sources: Literature
15 May 2017, Gel status: 0
Created
Helen Brittain (Genomics England Curator)SAMD9 was created by helen.brittain