Genes in panel
STRs in panel
Prev Next
Regions in panel
Prev Next

Hearing loss

Gene: CDKN2D

Red List (low evidence)

CDKN2D (cyclin dependent kinase inhibitor 2D)
EnsemblGeneIds (GRCh38): ENSG00000129355
EnsemblGeneIds (GRCh37): ENSG00000129355
OMIM: 600927, Gene2Phenotype
CDKN2D is in 1 panel

2 reviews

Maria Bitner-Glindzicz (UCL)

Red List (low evidence)

Jun Shen (Harvard Medical School)

Red List (low evidence)

CDKN2D is not associated with a phenotype entry in OMIM.
Created: 9 Feb 2016, 10:05 a.m.
CDKN2D is not associated with a phenotype entry in OMIM.
Created: 7 Feb 2016, 3:40 p.m.

Publications

Details

Sources
  • Expert
OMIM
600927
Clinvar variants
Variants in CDKN2D
Penetrance
Complete
Panels with this gene

History Filter Activity

24 Jun 2015, Gel status: 0

Added New Source

Ellen McDonagh (Genomics England Curator)

CDKN2D was added to Congenital hearing impairment (Profound/Severe)panel. Sources: Expert