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Hearing loss

Gene: LFNG

Red List (low evidence)

LFNG (LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase)
EnsemblGeneIds (GRCh38): ENSG00000106003
EnsemblGeneIds (GRCh37): ENSG00000106003
OMIM: 602576, Gene2Phenotype
LFNG is in 10 panels

1 review

Jun Shen (Harvard Medical School)

Red List (low evidence)

Mode of inheritance

#609813:?Spondylocostal dysostosis 3, autosomal recessive[<omim version=1.0><clinicalSynopsisList>]


History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

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