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Hearing loss

Gene: AP3D1

Red List (low evidence)

AP3D1 (adaptor related protein complex 3 delta 1 subunit)
EnsemblGeneIds (GRCh38): ENSG00000065000
EnsemblGeneIds (GRCh37): ENSG00000065000
OMIM: 607246, Gene2Phenotype
AP3D1 is in 7 panels

2 reviews

Maria Bitner-Glindzicz (UCL)

Red List (low evidence)

Jun Shen (Harvard Medical School)

Red List (low evidence)

AP3D1 is not associated with a phenotype entry in OMIM.
Created: 9 Feb 2016, 10:05 a.m.
AP3D1 is not associated with a phenotype entry in OMIM.
Created: 7 Feb 2016, 3:39 p.m.

Publications

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

AP3D1 was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert