Multiple Tumours
Gene: CTRCEnsemblGeneIds (GRCh38): ENSG00000162438
EnsemblGeneIds (GRCh37): ENSG00000162438
OMIM: 601405, Gene2Phenotype
CTRC is in 1 panel
1 review
Ellen McDonagh (Genomics England Curator)
On the UKGTN Hereditary Cancers 82 Gene Panel for Familial Pancreatic Cancer.Created: 18 Apr 2017, 1:41 p.m.
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
{Pancreatitis, chronic, susceptibility to} 167800
Details
- Mode of Inheritance
- MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
- Sources
-
- Expert Review Amber
- UKGTN
- Phenotypes
-
- {Pancreatitis, chronic, susceptibility to} 167800
- OMIM
- 601405
- Clinvar variants
- Variants in CTRC
- Penetrance
- Complete
- Publications
- Panels with this gene
History Filter Activity
Gene classified by Genomics England curator
Ellen McDonagh (Genomics England Curator)This gene has been classified as Amber List (Moderate Evidence).
Set publications
Ellen McDonagh (Genomics England Curator)Publications for CTRC were set to 24624459
Created
Ellen McDonagh (Genomics England Curator)CTRC was created by ellenmcdonagh
Added New Source
Ellen McDonagh (Genomics England Curator)CTRC was added to Multiple Tumourspanel. Sources: UKGTN