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Mendeliome

Gene: RNF139

Red List (low evidence)

RNF139 (ring finger protein 139)
EnsemblGeneIds (GRCh38): ENSG00000170881
EnsemblGeneIds (GRCh37): ENSG00000170881
OMIM: 603046, Gene2Phenotype
RNF139 is in 1 panel

1 review

Belinda Chong (Victorian Clinical Genetics Services)

Red List (low evidence)

Single variant identified in a tumor sample of a family with hereditary renal cell carcinoma.
Created: 13 May 2022, 4:03 a.m. | Last Modified: 13 May 2022, 4:03 a.m.
Panel Version: 0.14223

Mode of inheritance
Other

Phenotypes
Renal cell carcinoma MIM#144700

Publications

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Renal cell carcinoma MIM#144700
OMIM
603046
Clinvar variants
Variants in RNF139
Penetrance
None
Publications
Panels with this gene

History Filter Activity

16 May 2022, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: rnf139 has been classified as Red List (Low Evidence).

16 May 2022, Gel status: 1

Set Phenotypes

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Phenotypes for gene: RNF139 were changed from to Renal cell carcinoma MIM#144700

16 May 2022, Gel status: 1

Set publications

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Publications for gene: RNF139 were set to

16 May 2022, Gel status: 1

Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Mode of inheritance for gene: RNF139 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted

16 May 2022, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: rnf139 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: RNF139 was added gene: RNF139 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: RNF139 was set to Unknown