Gene therapy clinical trials
Gene: ADAEnsemblGeneIds (GRCh38): ENSG00000196839
EnsemblGeneIds (GRCh37): ENSG00000196839
OMIM: 608958, Gene2Phenotype
ADA is in 13 panels
1 review
Ellen McDonagh (Genomics England Curator)
Genetic: ADA lentiviral vector transduced patient Cd34+ cells - trial https://ClinicalTrials.gov/show/NCT01380990. Biological: Intravenous infusion of transduced cells - trial https://ClinicalTrials.gov/show/NCT01279720Created: 2 May 2018, 3:12 p.m.
Phenotypes
Adenosine deaminase (ADA) deficiency
Details
- Sources
-
- Expert Review Green
- ClinicalTrials.gov
- Phenotypes
-
- Adenosine deaminase (ADA) deficiency
- OMIM
- 608958
- Clinvar variants
- Variants in ADA
- Penetrance
- None
- Panels with this gene
-
- Likely inborn error of metabolism
- Haematological malignancies cancer susceptibility
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Fetal anomalies
- Severe combined immunodeficiency with adenosine deaminase deficiency
- COVID-19 research
- Undiagnosed metabolic disorders
- DDG2P
- Dystonia, chorea or related movement disorder, childhood onset
- Gastrointestinal epithelial barrier disorders
- Autoinflammatory disorders
- Infantile enterocolitis & monogenic inflammatory bowel disease
- Intellectual disability
History Filter Activity
Set penetrance
Ellen McDonagh (Genomics England Curator)Phenotypes for gene ADA were set to Adenosine deaminase (ADA) deficiency
Added New Source
Ellen McDonagh (Genomics England Curator)ADA was added to Gene therapy clinical trials panel. Sources: ClinicalTrials.gov,Expert Review Green
Created
Ellen McDonagh (Genomics England Curator)ADA was created by Ellen McDonagh