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Hearing loss

Gene: GFI1

Red List (low evidence)

GFI1 (growth factor independent 1 transcriptional repressor)
EnsemblGeneIds (GRCh38): ENSG00000162676
EnsemblGeneIds (GRCh37): ENSG00000162676
OMIM: 600871, Gene2Phenotype
GFI1 is in 6 panels

2 reviews

Maria Bitner-Glindzicz (UCL)

Red List (low evidence)

Jun Shen (Harvard Medical School)

Red List (low evidence)

Mode of inheritance
Unknown

Phenotypes
#607847:Neutropenia, nonimmune chronic idiopathic, of adults[<omim version=1.0><clinicalSynopsisList>]; #613107:Neutropenia, severe congenital 2, autosomal dominant[<omim version=1.0><clinicalSynopsisList>]

Publications

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

GFI1 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert