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Hearing loss

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 1 panel

1 review

Jun Shen (Harvard Medical School)

Red List (low evidence)

Mode of inheritance
Unknown

Phenotypes
#612237:Chondrosarcoma, extraskeletal myxoid[<omim version=1.0><clinicalSynopsisList>]

Publications

Details

Sources
  • Expert
OMIM
600542
Clinvar variants
Variants in NR4A3
Penetrance
Complete
Panels with this gene

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

NR4A3 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert