This Panel is marked as Deleted
Immunological disorders Victorian Clinical Genetics Services
Gene: ADA
ADA (adenosine deaminase)
EnsemblGeneIds (GRCh38): ENSG00000196839
EnsemblGeneIds (GRCh37): ENSG00000196839
OMIM: 608958, Gene2Phenotype
ADA is in 13 panels
EnsemblGeneIds (GRCh38): ENSG00000196839
EnsemblGeneIds (GRCh37): ENSG00000196839
OMIM: 608958, Gene2Phenotype
ADA is in 13 panels
0 reviews
Details
- Sources
-
- Victorian Clinical Genetics Services
- Expert Review Green
- OMIM
- 608958
- Clinvar variants
- Variants in ADA
- Penetrance
- None
- Panels with this gene
-
- Likely inborn error of metabolism
- Severe combined immunodeficiency with adenosine deaminase deficiency
- Haematological malignancies cancer susceptibility
- DDG2P
- COVID-19 research
- Undiagnosed metabolic disorders
- Intellectual disability
- Childhood onset dystonia, chorea or related movement disorder
- Autoinflammatory disorders
- Fetal anomalies
- Gastrointestinal epithelial barrier disorders
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Infantile enterocolitis & monogenic inflammatory bowel disease
History Filter Activity
12 Jun 2018, Gel status: 4
Added New Source
Sarah Leigh (Genomics England Curator)ADA was added to Immunological disorders Victorian Clinical Genetics Services panel. Sources: Expert Review Green,Victorian Clinical Genetics Services
12 Jun 2018, Gel status: 4
Created
Sarah Leigh (Genomics England Curator)ADA was created by Sarah Leigh