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Hearing loss

Gene: HOXA1

Red List (low evidence)

HOXA1 (homeobox A1)
EnsemblGeneIds (GRCh38): ENSG00000105991
EnsemblGeneIds (GRCh37): ENSG00000105991
OMIM: 142955, Gene2Phenotype
HOXA1 is in 6 panels

1 review

Jun Shen (Harvard Medical School)

Red List (low evidence)

Mode of inheritance

#601536:Bosley-Salih-Alorainy syndrome[<omim version=1.0><clinicalSynopsisList>]


History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

HOXA1 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert