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Hearing loss

Gene: ALDH1A2

Red List (low evidence)

ALDH1A2 (aldehyde dehydrogenase 1 family member A2)
EnsemblGeneIds (GRCh38): ENSG00000128918
EnsemblGeneIds (GRCh37): ENSG00000128918
OMIM: 603687, Gene2Phenotype
ALDH1A2 is in 2 panels

1 review

Jun Shen (Harvard Medical School)

Red List (low evidence)

ALDH1A2 is not associated with a phenotype entry in OMIM.
Created: 9 Feb 2016, 10:05 a.m.

Publications

Details

Sources
  • Expert
OMIM
603687
Clinvar variants
Variants in ALDH1A2
Penetrance
Complete
Panels with this gene

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

ALDH1A2 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert