Genes in panel
STRs in panel
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Monogenic hearing loss

Gene: FBXO2

Red List (low evidence)

FBXO2 (F-box protein 2)
EnsemblGeneIds (GRCh38): ENSG00000116661
EnsemblGeneIds (GRCh37): ENSG00000116661
OMIM: 607112, Gene2Phenotype
FBXO2 is in 1 panel

2 reviews

Maria Bitner-Glindzicz (UCL)

Red List (low evidence)

Jun Shen (Harvard Medical School)

Red List (low evidence)

FBXO2 is not associated with a phenotype entry in OMIM.
Created: 9 Feb 2016, 10:06 a.m.
FBXO2 is not associated with a phenotype entry in OMIM.
Created: 7 Feb 2016, 3:41 p.m.

Publications

Details

Sources
  • Expert
OMIM
607112
Clinvar variants
Variants in FBXO2
Penetrance
Complete
Panels with this gene

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

FBXO2 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert