Pharmacogenomics_Paediatric
Gene: CYP2D6EnsemblGeneIds (GRCh38): ENSG00000100197
EnsemblGeneIds (GRCh37): ENSG00000100197
OMIM: 124030, Gene2Phenotype
CYP2D6 is in 2 panels
2 reviews
David Metz (Royal Children's Hospital)
PMID: 18406467
Genotype-phenotype concordance from 2 weeks of age
PMID: 24458010
Strong evidence. Risk of toxicity from codeine, tramadol, (oxycodone) if ultrarapid metaboliser.
Insensitivity to codeine, tramadol, (oxycodone) if poor metaboliser.Created: 14 Aug 2020, 12:31 a.m. | Last Modified: 14 Aug 2020, 4:18 a.m.
Panel Version: 0.33
Mode of inheritance
Other
Publications
Details
- Mode of Inheritance
- Other
- Sources
-
- Expert Review Green
- Phenotypes
-
- Codeine, tramadol, oxycodone
- OMIM
- 124030
- Clinvar variants
- Variants in CYP2D6
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Set publications
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Publications for gene: CYP2D6 were set to 18406467
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: cyp2d6 has been classified as Green List (High Evidence).
Set Phenotypes
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Phenotypes for gene: CYP2D6 were changed from to Codeine, tramadol, oxycodone
Entity classified by Genomics England curator
Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)Gene: cyp2d6 has been classified as Green List (High Evidence).
Created, Added New Source, Set mode of inheritance, Set publications
David Metz (Royal Children's Hospital)gene: CYP2D6 was added gene: CYP2D6 was added to Pharmacogenomics_Paediatric. Sources: Other Mode of inheritance for gene: CYP2D6 was set to Other Publications for gene: CYP2D6 were set to 18406467