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Hearing loss

Gene: IFT88

Red List (low evidence)

IFT88 (intraflagellar transport 88)
EnsemblGeneIds (GRCh38): ENSG00000032742
EnsemblGeneIds (GRCh37): ENSG00000032742
OMIM: 600595, Gene2Phenotype
IFT88 is in 2 panels

1 review

Jun Shen (Harvard Medical School)

Red List (low evidence)

IFT88 is not associated with a phenotype entry in OMIM.
Created: 9 Feb 2016, 10:07 a.m.
IFT88 is not associated with a phenotype entry in OMIM.
Created: 7 Feb 2016, 3:42 p.m.

Publications

Details

Sources
  • Expert
OMIM
600595
Clinvar variants
Variants in IFT88
Penetrance
Complete
Panels with this gene

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

IFT88 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert