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Transplant Co-Morbidity Superpanel

Gene: PPIB

Green List (high evidence)

PPIB (peptidylprolyl isomerase B)
EnsemblGeneIds (GRCh38): ENSG00000166794
EnsemblGeneIds (GRCh37): ENSG00000166794
OMIM: 123841, Gene2Phenotype
PPIB is in 9 panels

0 reviews

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Osteogenesis imperfecta, type IX, MIM# 259440
OMIM
123841
Clinvar variants
Variants in PPIB
Penetrance
None
Publications
Panels with this gene

History Filter Activity

1 Aug 2023, Gel status: 3

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes

Bryony Thompson (Royal Melbourne Hospital)

gene: PPIB was added gene: PPIB was added to Transplant Co-Morbidity Superpanel. Sources: Victorian Clinical Genetics Services,Expert Review Green Mode of inheritance for gene: PPIB was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: PPIB were set to 32392875; 19781681 Phenotypes for gene: PPIB were set to Osteogenesis imperfecta, type IX, MIM# 259440