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Mendeliome

Gene: NR4A3

Red List (low evidence)

NR4A3 (nuclear receptor subfamily 4 group A member 3)
EnsemblGeneIds (GRCh38): ENSG00000119508
EnsemblGeneIds (GRCh37): ENSG00000119508
OMIM: 600542, Gene2Phenotype
NR4A3 is in 2 panels

1 review

Ain Roesley (Victorian Clinical Genetics Services)

Red List (low evidence)

currently no mendelian association has been reported
Created: 17 Nov 2021, 6:31 a.m. | Last Modified: 17 Nov 2021, 6:31 a.m.
Panel Version: 0.9763

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
OMIM
600542
Clinvar variants
Variants in NR4A3
Penetrance
None
Panels with this gene

History Filter Activity

28 Mar 2022, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: nr4a3 has been classified as Red List (Low Evidence).

28 Mar 2022, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: nr4a3 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: NR4A3 was added gene: NR4A3 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: NR4A3 was set to Unknown