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Hearing loss

Gene: GPX1

Red List (low evidence)

GPX1 (glutathione peroxidase 1)
EnsemblGeneIds (GRCh38): ENSG00000233276
EnsemblGeneIds (GRCh37): ENSG00000233276
OMIM: 138320, Gene2Phenotype
GPX1 is in 5 panels

2 reviews

Maria Bitner-Glindzicz (UCL)

Red List (low evidence)

Jun Shen (Harvard Medical School)

Red List (low evidence)

Mode of inheritance
BIALLELIC, autosomal or pseudoautosomal

Phenotypes
#614164:Hemolytic anemia due to glutathione peroxidase deficiency[Hemolytic disease of the newborn; Compensated hemolytic anemia; Neonatal hyperbilirubinemia; Glutathione peroxidase deficiency; Heinz bodies; Selenium deficiency interaction]

Publications

Details

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

GPX1 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert