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Mendeliome

Gene: BCL2

Red List (low evidence)

BCL2 (BCL2, apoptosis regulator)
EnsemblGeneIds (GRCh38): ENSG00000171791
EnsemblGeneIds (GRCh37): ENSG00000171791
OMIM: 151430, Gene2Phenotype
BCL2 is in 2 panels

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

No evidence for association with Mendelian disease.
Created: 1 May 2022, 7:36 a.m. | Last Modified: 1 May 2022, 7:36 a.m.
Panel Version: 0.13507

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
OMIM
151430
Clinvar variants
Variants in BCL2
Penetrance
None
Panels with this gene

History Filter Activity

1 May 2022, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: bcl2 has been classified as Red List (Low Evidence).

1 May 2022, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: bcl2 has been classified as Red List (Low Evidence).

17 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: BCL2 was added gene: BCL2 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: BCL2 was set to Unknown