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Mendeliome

Gene: MYC

Red List (low evidence)

MYC (MYC proto-oncogene, bHLH transcription factor)
EnsemblGeneIds (GRCh38): ENSG00000136997
EnsemblGeneIds (GRCh37): ENSG00000136997
OMIM: 190080, Gene2Phenotype
MYC is in 1 panel

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

Not associated with Mendelian disease.
Created: 14 Jul 2021, 6:03 a.m. | Last Modified: 14 Jul 2021, 6:03 a.m.
Panel Version: 0.8320

Mode of inheritance
Other

Phenotypes
Burkitt lymphoma, somatic, MIM# 113970

Details

Mode of Inheritance
Other
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Burkitt lymphoma, somatic, MIM# 113970
OMIM
190080
Clinvar variants
Variants in MYC
Penetrance
None
Panels with this gene

History Filter Activity

14 Jul 2021, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

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

14 Jul 2021, Gel status: 1

Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Phenotypes for gene: MYC were changed from to Burkitt lymphoma, somatic, MIM# 113970

14 Jul 2021, Gel status: 1

Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Mode of inheritance for gene: MYC was changed from Unknown to Other

14 Jul 2021, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

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