Transplant Co-Morbidity Superpanel
Gene: PPARGEnsemblGeneIds (GRCh38): ENSG00000132170
EnsemblGeneIds (GRCh37): ENSG00000132170
OMIM: 601487, Gene2Phenotype
PPARG is in 7 panels
0 reviews
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
- Sources
-
- Expert Review Green
- NHS GMS
- Phenotypes
-
- FPLD3
- Lipodystrophy, familial partial, type 3
- LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3
- Insulin resistance, severe, digenic
- Obesity, severe, 601665
- Carotid intimal medial thickness 1, 609338
- Lipodystrophy, familial partial, type 3, 604367
- {Diabetes, type 2}, 125853
- Lipodystrophy, familial partial, type 3 604367
- [Obesity, resistance to]
- Insulin resistance, severe, digenic 604367
- Diabetes Mellitus, Noninsulin-Dependent, with Acanthosis Nigricans and Hypertension
- Insulin resistance, severe, digenic, 604367
- OMIM
- 601487
- Clinvar variants
- Variants in PPARG
- Penetrance
- None
- Panels with this gene
History Filter Activity
Created, Added New Source, Set mode of inheritance, Set Phenotypes
Bryony Thompson (Royal Melbourne Hospital)gene: PPARG was added gene: PPARG was added to Transplant Co-Morbidity Superpanel. Sources: NHS GMS,Expert Review Green Mode of inheritance for gene: PPARG was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: PPARG were set to FPLD3; Lipodystrophy, familial partial, type 3; LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; Insulin resistance, severe, digenic; Obesity, severe, 601665; Carotid intimal medial thickness 1, 609338; Lipodystrophy, familial partial, type 3, 604367; {Diabetes, type 2}, 125853; Lipodystrophy, familial partial, type 3 604367; [Obesity, resistance to]; Insulin resistance, severe, digenic 604367; Diabetes Mellitus, Noninsulin-Dependent, with Acanthosis Nigricans and Hypertension; Insulin resistance, severe, digenic, 604367