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
-
- Infantile enterocolitis & monogenic inflammatory bowel disease
- Autoinflammatory disorders
- Haematological malignancies cancer susceptibility
- Undiagnosed metabolic disorders
- Severe combined immunodeficiency with adenosine deaminase deficiency
- Fetal anomalies
- Likely inborn error of metabolism
- Intellectual disability
- COVID-19 research
- Primary immunodeficiency or monogenic inflammatory bowel disease
- Childhood onset dystonia, chorea or related movement disorder
- DDG2P
- Gastrointestinal epithelial barrier disorders
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