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Mendeliome

Gene: ING3

Red List (low evidence)

ING3 (inhibitor of growth family member 3)
EnsemblGeneIds (GRCh38): ENSG00000071243
EnsemblGeneIds (GRCh37): ENSG00000071243
OMIM: 607493, Gene2Phenotype
ING3 is in 1 panel

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

Cannot find evidence for Mendelian gene-disease association.
Created: 3 Mar 2020, 1:34 a.m. | Last Modified: 3 Mar 2020, 1:34 a.m.
Panel Version: 0.1592

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
OMIM
607493
Clinvar variants
Variants in ING3
Penetrance
None
Panels with this gene

History Filter Activity

3 Mar 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: ing3 has been classified as Red List (Low Evidence).

3 Mar 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: ing3 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: ING3 was added gene: ING3 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: ING3 was set to Unknown