GT/TP identifiers for the NHSE Digital Genomic Test Service are temporarily visible in PanelApp but are not yet in use in Genomics England systems
  1. Panels
  2. Familial prostate cancer

Familial prostate cancer (Version 1.4)


Panel types: Rare Disease 100K
Previous code: 5763f2bf8f620350a1996047
Description
This panel is NO LONGER ACTIVELY MAINTAINED.

Please use with caution, as the gene list has not been recently updated. Reviews added to this panel are no longer a priority for curation and may not be followed up.

Please consider using an NHS Genomic Medicine Service (GMS) panel instead. The full list of GMS panels can be found here: https://nhsgms-panelapp.genomicsengland.co.uk/panels, with links back to PanelApp should you wish to leave a review on the panel.

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There is currently no eligibility criteria for this disorder.
Panel Activity

2 reviewers

  • Ellen McDonagh (Genomics England Curator)

    Group: Other
    Workplace: Other

  • Clare Turnbull (Queen Mary University London)

    Group: GeCIP domain
    Workplace: NHS clinical service

14 Entities

14 reviewed, 1 green

List Entity Reviews Mode of inheritance Details
14 Entitiess
Green List (high evidence)
BRCA2
2 reviews
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Green
Phenotypes
  • {Prostate cancer}, OMIM:176807
Tags
Amber List (moderate evidence)
BRCA1
2 reviews
1 green
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert list
  • Expert Review Amber
Phenotypes
  • Prostate cancer, MONDO:0008315
Tags
Red List (low evidence)
BRIP1
1 review
Unknown
Sources
  • Literature
Tags
Red List (low evidence)
CHEK2
1 review
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Literature
Phenotypes
  • {Prostate cancer, familial, susceptibility to}
Tags
Red List (low evidence)
ELAC2
1 review
Unknown
Sources
  • Literature
Phenotypes
  • hereditary prostate cancer
Tags
Red List (low evidence)
HOXB13
1 review
Unknown
Sources
  • Literature
Tags
Red List (low evidence)
MSH2
1 review
1 red
Unknown
Sources
  • Expert list
Tags
Red List (low evidence)
MSH5
1 review
Unknown
Sources
  • Literature
Phenotypes
  • prostate cancer susceptibility
Tags
Red List (low evidence)
MSH6
1 review
Unknown
Sources
  • Literature
Tags
Red List (low evidence)
MSR1
1 review
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Other
Phenotypes
  • Prostate cancer, hereditary
Tags
Red List (low evidence)
PALB2
1 review
Unknown
Sources
  • Literature
Tags
Red List (low evidence)
PTEN
1 review
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Other
Phenotypes
  • harmartoma, glioma, prostate, endometrial
  • Cowden syndrome, Bannayan-Riley-Ruvalcaba syndrome
Tags
Red List (low evidence)
RNASEL
1 review
Unknown
Sources
  • Literature
Phenotypes
  • hereditary prostate cancer
Tags
Red List (low evidence)
SPOP
1 review
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Other
Phenotypes
  • prostate cancer
Tags

Major version comments

  • 07/03/2017 - revised and ready to promote to version 1.

Downloads

Download lists

  • Whole panel
  • Green list (high evidence)
  • Green and Amber Genes
  • Amber Genes
  • Red list (low evidence)

Download Version