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Hearing loss

Gene: AXIN1

Red List (low evidence)

AXIN1 (axin 1)
EnsemblGeneIds (GRCh38): ENSG00000103126
EnsemblGeneIds (GRCh37): ENSG00000103126
OMIM: 603816, Gene2Phenotype
AXIN1 is in 2 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
#114550:Hepatocellular carcinoma, somatic[Hepatocellular carcinomaMicronodular cirrhosisSubacute progressive viral hepatitis; Primary liver cancer; Often integrated HBV sequences in hepatocellular carcinomas]; #607864:?Caudal duplication anomaly[<omim version=1.0><clinicalSynopsisList>]

Publications

Details

Sources
  • Expert
OMIM
603816
Clinvar variants
Variants in AXIN1
Penetrance
Complete
Panels with this gene

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

AXIN1 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert