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Hearing loss

Gene: CASP3

Red List (low evidence)

CASP3 (caspase 3)
EnsemblGeneIds (GRCh38): ENSG00000164305
EnsemblGeneIds (GRCh37): ENSG00000164305
OMIM: 600636, Gene2Phenotype
CASP3 is in 3 panels

2 reviews

Maria Bitner-Glindzicz (UCL)

Red List (low evidence)

Jun Shen (Harvard Medical School)

Red List (low evidence)

CASP3 is not associated with a phenotype entry in OMIM.
Created: 9 Feb 2016, 10:05 a.m.
CASP3 is not associated with a phenotype entry in OMIM.
Created: 7 Feb 2016, 3:40 p.m.

Publications

Details

Sources
  • Expert
OMIM
600636
Clinvar variants
Variants in CASP3
Penetrance
Complete
Panels with this gene

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

CASP3 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert