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Hearing loss

Gene: PRRX2

Red List (low evidence)

PRRX2 (paired related homeobox 2)
EnsemblGeneIds (GRCh38): ENSG00000167157
EnsemblGeneIds (GRCh37): ENSG00000167157
OMIM: 604675, Gene2Phenotype
PRRX2 is in 1 panel

1 review

Jun Shen (Harvard Medical School)

Red List (low evidence)

PRRX2 is not associated with a phenotype entry in OMIM.
Created: 9 Feb 2016, 10:08 a.m.
PRRX2 is not associated with a phenotype entry in OMIM.
Created: 7 Feb 2016, 3:45 p.m.

Publications

Details

Sources
  • Expert
OMIM
604675
Clinvar variants
Variants in PRRX2
Penetrance
Complete
Panels with this gene

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

PRRX2 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert