Transplant Co-Morbidity Superpanel
Gene: CYP4F2EnsemblGeneIds (GRCh38): ENSG00000186115
EnsemblGeneIds (GRCh37): ENSG00000186115
OMIM: 604426, Gene2Phenotype
CYP4F2 is in 1 panel
1 review
Claire Fryer-Smith (University of Melbourne)
It is involved in guidelines for warfarin
https://www.pharmgkb.org/gene/PA27121/overview
Sources: Expert listCreated: 25 Aug 2023, 4:40 a.m.
Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Warfarin dosage sensitivity MIM# 122700
Publications
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Phenotypes
-
- Warfarin dosage sensitivity MIM# 122700
- OMIM
- 604426
- Clinvar variants
- Variants in CYP4F2
- Penetrance
- None
- Publications
- Panels with this gene
History Filter Activity
Entity classified by Genomics England curator
Bryony Thompson (Royal Melbourne Hospital)Gene: cyp4f2 has been classified as Green List (High Evidence).
Entity classified by Genomics England curator
Bryony Thompson (Royal Melbourne Hospital)Gene: cyp4f2 has been classified as Green List (High Evidence).
Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes
Claire Fryer-Smith (University of Melbourne)gene: CYP4F2 was added gene: CYP4F2 was added to Transplant Co-Morbidity Superpanel. Sources: Expert list Mode of inheritance for gene: CYP4F2 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: CYP4F2 were set to 25370453; 20555338; 19207028; 18250228 Phenotypes for gene: CYP4F2 were set to Warfarin dosage sensitivity MIM# 122700 Review for gene: CYP4F2 was set to GREEN