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Hearing loss

Gene: RARA

Red List (low evidence)

RARA (retinoic acid receptor alpha)
EnsemblGeneIds (GRCh38): ENSG00000131759
EnsemblGeneIds (GRCh37): ENSG00000131759
OMIM: 180240, Gene2Phenotype
RARA is in 2 panels

1 review

Jun Shen (Harvard Medical School)

Red List (low evidence)

Mode of inheritance
Unknown

Phenotypes
#612376:Leukemia, acute promyelocytic[<omim version=1.0><clinicalSynopsisList>]

Publications

Details

Sources
  • Expert
OMIM
180240
Clinvar variants
Variants in RARA
Penetrance
Complete
Panels with this gene

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

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