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  2. Incidentalome_PREGEN_DRAFT
  3. CDH1
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Incidentalome_PREGEN_DRAFT

Gene: CDH1

Amber List (moderate evidence)
CDH1 (cadherin 1)
EnsemblGeneIds (GRCh38): ENSG00000039068
EnsemblGeneIds (GRCh37): ENSG00000039068
OMIM: 192090, Gene2Phenotype
CDH1 is in 9 panels

1 review

Tony Roscioli (New South Wales Health Pathology)

I don't know

Comment on list classification: Needs review by PreGen committee - a cause for syndromic Clefting but also for later onset gastric cancer with incomplete overlap of gen phen correlations
Created: 7 Jan 2021, 1:25 a.m. | Last Modified: 7 Jan 2021, 1:25 a.m.
Panel Version: 0.14
A cause of syndromic orofacial clefting but may cause gastric cancer - needs discussion
Created: 4 Dec 2020, 4:14 a.m. | Last Modified: 4 Dec 2020, 4:14 a.m.
Panel Version: 0.3
Created: 4 Dec 2020, 4:14 a.m.
Last Modified: 4 Dec 2020, 4:14 a.m.
Panel version: 0.3

History Filter Activity

7 Jan 2021, Gel status: 2

Entity classified by Genomics England curator

Tony Roscioli (New South Wales Health Pathology)

Gene: cdh1 has been classified as Amber List (Moderate Evidence).

7 Jan 2021, Gel status: 2

Entity classified by Genomics England curator

Tony Roscioli (New South Wales Health Pathology)

Gene: cdh1 has been classified as Amber List (Moderate Evidence).

9 Nov 2020, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: CDH1 was added gene: CDH1 was added to Incidentalome_NSW. Sources: Expert Review Green,NSW Health Pathology Mode of inheritance for gene: CDH1 was set to Unknown