Multiple Tumours
Gene: PRSS2EnsemblGeneIds (GRCh38): ENSG00000275896
OMIM: 601564, Gene2Phenotype
PRSS2 is in 1 panel
2 reviews
Eleanor Williams (Genomics England Curator)
Ensembl identifier not available for GRCh37 (release 82)Created: 8 Jul 2020, 2:03 p.m. | Last Modified: 8 Jul 2020, 2:03 p.m.
Panel Version: 1.95
Ellen McDonagh (Genomics England Curator)
On the UKGTN Hereditary Cancers 82 Gene Panel for Familial Pancreatic Cancer.Created: 18 Apr 2017, 1:50 p.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
{Pancreatitis, chronic, protection against} 167800
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
- Sources
-
- Expert Review Amber
- UKGTN
- Phenotypes
-
- {Pancreatitis, chronic, protection against} 167800
- Tags
- OMIM
- 601564
- Clinvar variants
- Variants in PRSS2
- Penetrance
- Complete
- Panels with this gene
History Filter Activity
Added Tag
Eleanor Williams (Genomics England Curator)Tag ensembl_ids_known_missing tag was added to gene: PRSS2.
Gene classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)This gene has been classified as Amber List (Moderate Evidence).
Created
Ellen McDonagh (Genomics England Curator)PRSS2 was created by ellenmcdonagh
Added New Source
Ellen McDonagh (Genomics England Curator)PRSS2 was added to Multiple Tumourspanel. Sources: UKGTN